Working PaperPDF Available

Spirulina in combating Protein Energy Malnutrition (PEM) and Protein Energy Wasting (PEW) - A review

Authors:

Figures

Content may be subject to copyright.
J Nut Res (2015) 3(1): 62-79
ISSN: 2348-1064
Abstract
Spirulina, is a simple extract of blue-green algae, which is now
used worldwide as a food product and as a dietary supplement. It
contains, essential amino acids, lipids, vitamins, minerals and
anti-oxidants and can be considered as a wholesome food
supplement. Spirulina contains, approximately, 65% to 71%
protein by dry weight and is claimed to be non toxic nutritious
food with exceptional properties. A large amount of scientific
literature available about Spirulina and its usage in treatment of
child malnutrition, nutrition rehabilitation of HIV-infected,
cancer patients, hepato-protective effects etc. However, there is
no specific review available which gives more emphasis on the
protein and energy content and its effects. In the present work, we
reviewed several papers and reports and paid more attention on
protein content, which is the major constituent of Spirulina and
its effect on various disease conditions and possibility of using
Spirulina in combating against Protein Energy Malnutrition
(PEM) and Protein Energy Wasting (PEW). This work is of
certain significance for nutritionists, doctors and public health
workers involved in combating malnutrition. The risks involved
and optimal intake level for humans and animals are discussed in
detail.
Keywords: Protein Energy Malnutrition (PEM):Protein Energy
Wasting (PEW):Spirulina¸ Toxicity.
Introduction
It is not accurately known when people started using microalgae
as food source or food supplement but the first recorded evidence
is from Bernal Diaz del Castillo, a member of Heman Cortez‟s
(Spanish conquistador) troops, reported in 1520, in Tenochtitlan
(today Mexico City):that S. maxima was harvested from the lake
Texcoco, dried and sold for human consumption. Native
Mexicans called it as Tecuitlalt, meaning “excrements of stones”.
The topic of the Tecuitlalt, which was earlier discovered in 1520,
was not mentioned again until 1940, the French phycologist
Pierre Dangeard mentioned about a cake called “dihe”, consumed
by Kanembu tribe, African Lake Chad, Kanem (Chad, Africa).
Dangeard studied the dihe” samples and found that it is like a
puree of spring form blue algae (Sánchez et al. 2003).
The first unialgal culture achieved by Beijerinck in 1890 and
cultivation only started in 1919 by Otto Warburg‟s (Richmond
2008). Otto Warburg is well known for his work on Chlorella and
his aim is to understand and use them as a model for physiology
and photosynthesis research and not as a potential food source.
He used microalgae, Chlorella, because of its fast growing, non-
motile and simple life cycle properties. Warburg's study was
important because he was able to understand the number of
quantas required to possess photosynthesis and he also proposed
the concept of light utilization efficiency and conversion of light
to chemical energy (Richmond 2008).
During 1964 and 1965, the botanist Jean Leonard, during his
Belgian Trans-Sabaran Expedition, confirmed that dihe is made
up of Spirulina and thus chemical analysis was started on
Spirulina (Sanchez, 2003). During that time, Léonard received a
request from Sosa-Texcoco Ltd, Mexico to study a bloom of
algae in their sodium hydroxide production facility. As a result,
the first systematic and detailed study of the growth requirements
and physiology of Spirulina was performed. This study, which
was a part of Ph.D. thesis by Zarrouk (1966):was the basis for
establishing the first large-scale production plant of Spirulina
(Habib et al. 2008).
A single cell protein, which is nothing but a protein derived from
culture of single celled organisms, has gained popularity as
alternative food source during World War 1 and World War II.
After the formation of United Nations in the post war period,
hunger and malnutrition problems were highlighted by the Food
and Agriculture Organization of United Nations and has
introduced the concept of protein gap and reported that 25% of
Spirulina in combating Protein Energy Malnutrition (PEM) and
Protein Energy Wasting (PEW) - A review
Siva Kiran RR, Madhu GM*, Satyanarayana SV
Received: 10 March 2015 / Received in revised form: 17 December 2015, Accepted: 02 February 2016, Published online: 10 February 2016
© The Society for Clinical Nutrition and Metabolism 2013-2016
Siva Kiran RR, Madhu GM*
Department of Chemical Engineering, M.S. Ramaiah Institute of
Technology, Bangalore-560054
*Email: gmmadhu@gmail.com
Satyanarayana SV
Department of Chemical Engineering, JNTU College of
Engineering, Anantapur-515002
J Nut Res (2015) 3(1): 62-79
63
Composition Per 100 g
Companies
Earthrise
Nutrionals,
USA
DIC LIFETEC
Co. Ltd. Japan
(Hainan-DIC
Microalgae Co.
Ltd. China)
Parry
Nutraceuticals,
India
Nutrex Hawaii,
USA
Foundation
Antenna
Technologies,
Switzerland
1. Macronutrients
Calories (kcal)
373
386
410
333
Total fat
5.6 g
8.2 g
5 to 6 g
5 g
4 - 7 g
Myristic (C 14:0)
10 mg
16.4 mg
10-30 mg
40 mg
Palmitic (C 16:0)
2440 mg
3632 mg
2000 - 2500 mg
6100 mg
1032 - 1806 mg
Palmitoleic (C 16:1)
330 mg
237.8 mg
594 mg
152 - 266 mg
Heptadecanoic (C17:0)
20 mg
24.6 mg
Stearic (C18:0)
80 mg
90.2 mg
10 - 50 mg
250 mg
68 - 119 mg
Oleic (C18:1)
120 mg
246 mg
100 - 200 mg
51 mg
664 - 1162 mg
Linoleic (C18:2)
970 mg
2000 mg
750 -1200 mg
3300 mg
480 - 840 mg
Gamma-Linolenic (C18:3)
1350 mg
1238 mg
1000 - 1500 mg
3200 mg
1604 - 2807 mg
Others (C20)
140 mg
715 mg
Total carbohydrate
17.8 g
12.7 g
15 to 25 g
16 g
15 - 25 g
Dietary fiber
7.7 g
8.3 g
7 g
4 - 7 g
Sugars
1.3 g
4.4
9 g
Lactose
<0.1 g
-
Protein
63 g
69.4 g
56 to 69 g
67 g
55 - 70 g
Ash
< 9 %
5.6 %
6 to 9 g
8 - 13 g
7 - 13 g
Moisture
< 7 %
< 4.1 %
2.5 to 4.5 %
3 - 6 g
3 - 7 g
Essential amino acids
Histidine
1000 mg
1170 mg
500 - 1500 mg
1500 mg
1000 mg
Isoleucine
3500 mg
3480 mg
3000 - 4000 mg
3260 mg
3500 mg
Leucine
5380 mg
5610 mg
3000 - 5000 mg
4890 mg
5400 mg
Lysine
2960 mg
3080 mg
3000 - 6000 mg
2620 mg
2900 mg
Methionine
1170 mg
1590 mg
1000 - 6000 mg
1330 mg
1400 mg
Phenylalanine
2750 mg
2870 mg
2500 - 3500 mg
2610 mg
2800 mg
Threonine
2860 mg
3300 mg
1500 - 3000 mg
2810 mg
3200 mg
Tryptophan
1090 mg
1100 mg
1000 - 2000 mg
8500 mg
900 mg
Valine
3940 mg
3900 mg
1000 - 3000 mg
3740 mg
4000 mg
Nonessential amino acids
Alanine
4590 mg
4910 mg
4000 - 5000 mg
4660 mg
4700 mg
Arginine
4310 mg
4190 mg
3000 - 5000 mg
4760 mg
4300 mg
Aspartic acid
5990 mg
6180 mg
1500 - 3000 mg
7280 mg
6100 mg
Cystine
590 mg
700 mg
500 - 750 mg
5600 mg
600 mg
Glutamic acid
9130 mg
9290 mg
6000 - 9000 mg
8440 mg
9100 mg
Glycine
3130 mg
3210 mg
2000 - 4000 mg
3190 mg
3200 mg
Proline
2380 mg
2400 mg
2000 - 3000 mg
2470 mg
2700 mg
Serine
2760 mg
3210 mg
3000 - 4500 mg
2650 mg
3200 mg
Tyrosine
2500 mg
2740 mg
1000 - 2000 mg
2380 mg
3000 mg
2. Vitamins
Vitamin A
352000 IU
18000mcg
11250 IU
Vitamin K
1090 mcg
2220 mcg
0.90 - 1.05 mg
2500 mcg
2.24 mg
Vitamin C
0 mg
0 mg
-
0 mg
traces
Vitamin E
10 IU
10.6 mg
9500 mcg
10 mg
Vitamin B1 (Thiamine HCl)
0.5 mg
4.82 mg
0.15 - 0.30 mg
117 mcg
3.5 mg
Vitamin B2 (Riboflavin)
4.53 mg
3.93 mg
4.0 - 7.0 mg
4667 mcg
4 mg
Vitamin B3 (Niacin)
14.9 mg
39.3 mg
10.0 - 25.0 mg
13330 mcg
14 mg
Vitamin B6 (Pyridox. HCl)
0.96 mg
0.91 mg
0.5 - 1.5 mg
1000 mcg
0.8 mg
Vitamin B12
162 mcg
0.24 mg
0.10 - 0.30 mg
300 mcg
0.32 mg
Biotin
5 mcg
32.3 mcg
17 mcg
0.005 mg
Folic acid
10 mcg
73 mcg
0.05 - 0.30 mg
206 mcg
0.01 mg
Phantothenic acid
100 mcg
1.23 mg
150 mcg
0.1 mg
Inositol
64 mg
103 mg
70 - 90 mg
57 mg
64 mg
3. Minerals
Calcium
468 mg
70.5 mg
60 - 110 mg
334 mg
1000 mg
Iron
87.4 mg
83.3 mg
25 - 100 mg
217 mg
180 mg
Phosphorus
961 mg
921 mg
700 - 1000 mg
1100 mg
800 mg
Iodine
142 mcg
0.2 - 0.4 mg
500 mcg
Magnesium
319 mg
278 mg
200 - 300 mg
500 mg
400 mg
Zinc
1.45 mg
1.04 mg
1.0 - 3.0 mg
3 mg
30 mg
Selenium
25.5 mcg
-
0.003 - 0.010 mg
0.03 mg
0.01 - 0.04 ppm
64
J Nut Res (2015) 3(1): 62-79
world‟s population has a deficiency of protein intake in their diet.
Many research projects on yeast, chlorella, Spirulina, some
bacteria and moulds for large scale production of “single cell
proteins” were launched. In 1950, the United States and Japan
began the experimental cultivations of this microorganism to
investigate its chemical composition and industrial applications.
Studies were accelerated after the release of the book, Algal
Culture from Laboratory to Pilot Plant (Burlew, 1953):which
triggered research work around the globe (Richmond, 2008).
Japan was the first country to produce Chlorella based diet food
(Sanchez, 2003). Spirulina, in 1967 was established as a
“wonderful food source” by the International Association of
Applied Microbiology.
The first pilot plant which produced 150 tonnes of dry Spirulina
biomass per year started production in 1973; its production
capacity was thereafter raised to 300 tonnes of medium-grade
product per year from 12.0 hectares of natural ponds by Sosa-
Texcoco Ltd, Mexico. The annual value of Spirulina production
represented a third of the company's income from the
manufacture of powdered soda from the lake deposits. In 1995,
Sosa-Texcoco ceased production of Spirulina. The only remnant
today, Lake Texcoco, still has a living algae Spirulina population.
From 1970, the nutritional and medicinal studies on Spirulina
have been extensively studied along with its applications in water
treatment. According to the national report received by Food and
Agriculture Organization (FAO):United Nation, the production of
algae culture was greater than 68000 tons in 2008 and major
contribution from China and Chile. China started to produce
Spirulina through factories in 1990 and there were more than 80
factories by 1997 (Habib et al. 2008). Spirulina is produced in at
least 30 countries (Australia, Bangladesh, Benin, Brazil, Burkina
Faso, Chad, Chile, China, Costa Rica, Côte d'Ivoire, Cuba,
Ecuador, France, India, Israel, Italy, Japan, Madagascar,
Martinique, Mexico, Myanmar, Philippines, Peru, Portugal,
Spain, Thailand, Togo, United States of America and Vietnam)
(Habib et al. 2008).
Benefits of Spirulina
Spirulina does not need fertile land and has an advantage of
having rapid growth within 20 days, takes less energy input and
less water per kilo than soya, corn proteins and is environmental
friendly as there is possibility of recycling water after harvesting
and produce more oxygen than trees per acre by consuming
carbon dioxide (H.E. Remigio M. Maradona 2008).
Very few studies were found to describe the actual respiration
rate of Spirulina Sp. and in the below analysis, we could able to
collect some information to prove Spirulina produces more
oxygen than trees per acre. The notations used to measure trees
size is “dbh”. dbh refers to the tree diameter measured at 4.5 feet
above the ground and based on a study conducted on trees and
their oxygen release rates by David et al. (2007):trees with 1 - 3
inch - dbh produce 2.9 kg O2/per year; 9-12 inch dbh: 22.6 kg
O2/year; 18-21 inch dbh: 45.6 kg O2/year; 27-30 inch dbh; 91.1
kg O2/year and greater than 30 inch dbh 110.3 kg/O2 year. With
reference to the data reported by Dinesh et al. (2010):after
calculations, 42 ft2 area with 1000 L can produce approx. 20.717
kg oxygen per year with cell concentration varying from 1 * 105
to 5 * 105 cells per ml and 200 ft2 area with 4000 L, can produce
approx. 100 kg oxygen per year, if cell concentration per ml
increases, still increase in the rate of oxygen release can be
achieved. With reference to the respiration rate reported by Rym
(2012):115.89 kg O2 per year and as per Ohira et al. (1998):5.676
kg O2 per year per 150 grams dry weight Spirulina, can be
Copper
0.47 mg
0.26 mg
0.2 - 0.4 mg
0.67 mg
1.2 mg
Manganese
3.26 mg
3.81 mg
1.0 - 3.0 mg
13.3 mg
5 mg
Boron
1000 mcg
0.733 mg
Chromium
<400 mcg
0.39 mg
0.1 - 0.3 mg
1.34mg
0.28 mg
Molybdenum
1000 mcg
< 400 mcg
Potassium
1660 mg
1520 mg
1000 - 1500 mg
2000 mg
1400 mg
Sodium
641 mg
210 mg
700 - 1000 mg
1000 mg
900 mg
4. Phytonutrients
Phycocyanin
14000 mg
6550 mg
14000 - 16000 mg
8000 mg
15000 mg
Chlorophyll
1000 mg
1220 mg
1100 -1500 mg
1000 mg
1100 mg
Superoxide dismutase (SOD)
531000 IU
1000unit/g
3600 units
Gamma linolenic acid (GLA)
1080 mg
1067 mg
1300 mg
Total carotenoids
504 mg
360 - 500 mg
500 mg
370 mg
β-carotene
211 mg
216 mg
140 - 200 mg
227 mg
140 mg
Other Carotenes
30 mg
Zeaxanthin
101 mg
114 mg
125 - 200 mg
300 mg
Xanthophylls
170 mg
180 - 300 mg
Myxoxanthophyll
70 mg
Zeaxanthin
60 mg
Cryptoxanthin
10 mg
Echinenone
10 mg
Other Xanthophylls
20 mg
Sulfolipids
100 mg
Glycolipids
2000 mg
5. Other Minerals
Arsenic
< 1 ppm
-
< 0.50 ppm
< 0.5 ppm
0.06 - 2 ppm
Cadmium
< 0.5 ppm
< 0.20 ppm
<0.2 ppm
0.01 - 0.1 ppm
Mercury
< 0.05 ppm
< 0.05 ppm
<0.025 ppm
0.01 = 0.2 ppm
Lead
\< 2.5 ppm
-
< 0.2 ppm
<0.2 ppm
0.6 - 5.1 ppm
Germanium
60 mcg
Silicon
743 ppm
Sulfur
0.69 g
Cobalt
0.30 ppm
Fluorene
112-630 ppm
J Nut Res (2015) 3(1): 62-79
65
produced. It is quite evident based on the above scientific data
that Spirulina produce more oxygen than trees per acre.
Spirulina and its nutritional composition
The common name, Spirulina, refers to the dried biomass of
Arthrospira platensis, (Gershwin and Belay 2007):which belongs
to the oxygenic photosynthetic bacteria that cover the groups
Cyanobacteria and Prochlorales. These photosynthetic
organisms, Cyanobacteria, were first considered as alge until
1962 and for the first time, these blue green algae were added to
prokaryote kingdom and proposed to call these microorganisms
as Cyanobacteria (Stanier and Van Neil 1962):where algae is
considered to be a very large and diverse group of eukaryotic
organisms. This designation was accepted and published in 1974
by the Bergey's Manual of Determinative Bacteriology, which is
worldwide considered as a bible for biologists (Sánchez et al.
2003). Scientifically, there is a quite distinction between
Spirulina and Arthrospira genus. Stizenberger, in 1852 gave the
name Arthrospira based on the septa presence, helical form and
multicellular structure and Gomont in 1892, confirmed aseptate
form of the Spirulina genus. Geitler in 1932, reunified both
members designating them as Spirulina without considering the
septum. The worldwide research on microalgae was carried out in
the name of Spirulina, but the original species exploited as food
with excellent health properties belongs to genus Arthrospira.
This common difference between scientists and customers is
difficult to change (Sánchez et al. 2003). These Arthrospira
genus, constitute a helical trichomes of varying size and with
various degree of coiling including tightly coiled morphology to
even straight uncoiled form. The filaments are solitary and
reproduce by binary fission and the cells of the trichomes vary
from 2 µm to 12 µm and can sometime reach up to 16 µm.
Species of the genus Arthrospira have been isolated from alkaline
brackish and saline waters in tropical and subtropical regions.
Among the various species included in the genus Arthrospira, A.
platensis is the most widely distributed and is mainly found in
Africa but also in Asia. Arthrospira maxima is believed to be
found in California and Mexico (Gershwin 2007).
Since, 1970, Spirulina was analyzed physically and chemically
and numerous properties were evaluated. Based on the nutrition
profile listing of various multi-national global players, Spirulina
contains approximately 65 to 70% proteins, 15 to 25%
carbohydrates, 4 to 9 % fats and remaining vitamins, minerals,
pigments and very few toxic contaminations. In this article, the
main focus is review of all the works carried out on protein
content for combating against Protein Energy Malnutrition (PEM)
and Protein Energy Wasting (PEW) around the globe is discussed
in detail.
Comparision of protein content in Spirulina with other foods
Spirulina contains more natural proteins when compared with
other natural foods (Table 2). The true protein digestibility and
the biological activity of Spirulina protein calculated by
Narasimha et al. (1982) is 75.5 and 68 respectively. The
Recommended Dietary Allowance (RDA) for protein
consumption is 0.8g/kg body weight and for athletes, RDA ranges
from 1.2 to 1.4 g/kg/day (Otten et al. 2006). The advantage of
Spirulina protein can withstand without denaturating up to 670C
(Sánchez et al. 2003).
Table 2: Comparision of protein content of other foods with Spirulina
(Henrikson 1994)
Food Type
Crude Protein (%)
Spirulina powder
65 to 70
Whole Dried egg
47
Skimmed powdered milk
37
Whole soybean flour
36
Peanuts
26
Chicken
24
Fish
22
Beef meat
22
Cereal flours
<12
Vegetables
< 5
Risk assessment of Spirulina
Extensive care should be taken while consuming or prescribing
Spirulina as a protein source. Spirulina has more vitamin A, in
terms of beta carotenes, when compared with any natural foods
and care should be taken while administrating Spirulina that it
should not exceed the Recommended Dietary Allowance (RDA)
of 400 mcg to 900 mcg for normal adult male or female, where as
lactation stage, it can go up to 1300 mcg per day. Daily intake of
Vitamin A >25,000 IU for >6 years an >100,000 IU for >6
months are considered toxic (Fairfield and Fletcher 2002). 100
grams of Spirulina, contains greater than 353000 IU (Gershwin
and Belay 2007) and based on the recommended dietary
allowance of Vitamin A, it is recommended to consume only 7
grams of Spirulina per day which contains 25000 IU and children
less than 6 years to 6 months can take 25 grams of Spirulina per
day.
Excessive consumption of vitamin K, up to 0.2 g/kg body weight
does not show any toxic effect on rats (Molitor and Robinson
1940) and recommended RDA for vitamin K is >19 years, 90
mcg per day and >6 months to 12 months, 2.5 mcg per day and it
varies between 30 mcg to 60 mcg for 1 to 19 years. With
reference to these values, <1 year to 6 months kids, it is
recommended to give 4 grams of Spirulina per day for adults
which contributes about 90 mcg vitamin K and < 2 grams for 1
year to 6 months kids. Based on the composition, other vitamins
are within RDA limit per 10 grams of Spirulina powder. After
observing, RDA for adults for minerals, calcium (1300 mg):iron
(10 mg):iodine (150mcg): phosphorus (700mg):Magnesium (420
mg):Zinc (11 mg):Selenium (0.055 mg):Copper (0.9
mg):Manganese (2.3 mg):Boron (1000 to 10000
mcg):Germanium (1.5 mg) (Schauss 1991):Potassium (4700 mg)
and Sodium (1500 mg):most of them are within the range for
consumption of 100 grams of Spirulina. Based on RDA values
for chromium (35 mcg) and molybdenum (45 mcg) are safe for
10 grams of Spirulina per day. Coming to the pigments,
phycocyanin at 0.25 to 5.0 g/kg body weight have not shown any
toxic effect in rats (Naidu et al. 1999) and GLA can be consumed
up to 1.6 g per day. RDA recommends 30 to 45 grams of
carbohydrates per meal and maximum of 195 grams per day and
maximum of 40 % of calories coming from carbohydrates and
fats about 20 to 60 g per day for an average adult (Dietary
Reference Intakes, 2004).
Overall, based on the complete nutritional assessment, normal
healthy adult can take < 4 grams of Spirulina per day. But, it is
found that there is no toxic effect on rats, when consumed greater
than 0.8 g/kg of pure Spirulina powder (Krishnakumari et al.
1981). Based on the nutritional facts and composition and RDA
values, it is recommended to take < 4 grams of Spirulina per day
for healthy adult due to the presence of excess Vitamin A and not
66
J Nut Res (2015) 3(1): 62-79
more than 10 grams as it exceeds the RDA values of heavy
metals (Table 3).
The black color in the Table 3 shows that the particular nutrient
exceeds the RDA value. It was not colored black at 4 grams at
Vitamin A and Vitamin B, even though they are exceeding the
RDA values as the Vitamin A, upper limit is 7500 mcg and
Vitamin B, there is no upper limit (Dietary Reference Intakes,
2004). Chromium, molybdenum and vitamin A are exceeding
RDA values at 10 grams of Spirulina and at 15 grams
consumption, vitamin K is exceeding and at 25 grams, Iron was
exceeding RDA value and at 100 grams, protein, manganese,
phosphorous, vitamin B2 are exceeding and at 200 grams,
vitamin E, B3, B6, copper, iodine and magnesium are exceeding
and at 500 grams, calcium, vitamin B1, potassium and sodium are
exceeding RDA and it is strongly recommended to consume less
than 4 grams per day for an average healthy adult to avoid any
toxic effect based on the above scientific data. Care should be
taken while consuming and data related to cobalt and fluorine in
water used for Spirulina production was not reported by many
companies and these contents will also affect the quality of
Spirulina along with arsenic, lead, cadmium, mercury and silicon
concentrations. We believe that the above Table 3 will give basic
idea about Spirulina and risks involved in consumption and
industries should take care while preparing formulations or food
fortification products using Spirulina.
Protein Energy Malnutrition (PEM)
The World Health Organization (WHO) defines malnutrition as
„„the cellular imbalance between the supply of nutrients and
energy and the body‟s demand for them to ensure growth,
maintenance, and specific functions” and Protein Energy
Malnutrition (PEM) refers to a form of malnutrition, where there
is inadequate calorie or protein intake. Malnutrition is present in
both developed as well as under developing nations. Due to lack
of adequate food supply caused by socio-economical, political
and environmental factors, malnutrition was prevalent in
developing countries and in developed countries 6 to 51% of
hospitalized children were found to be malnourished (Grover and
Ee 2009).
Table 3: Risk assessment of spirulina based on US-RDA values for healthy adults (19 to 50) years and the black color indicates excess than RDA
Nutrients
US - RDA
(RDI, 2004)
Consumption pattern (per day)
4 gram
10 grams
15 grams
25 grams
100 grams
200 grams
500 grams
Total fat
20-35 g
0.224 g
0.56 g
0.84 g
1.4 g
5.6 g
11.2 g
28 g
Linoleic (C18:2)
10-17 g
0.0388 g
0.097 g
0.1455 g
0.2425 g
0.97 g
1.94 g
4.85 g
Total carbohydrate
130 g
0.712 g
1.78 g
2.67 g
4.45 g
17.8 g
35.6 g
89 g
Fibre
38 g
0.308 g
0.77 g
1.155 g
1.925 g
7.7 g
15.4 g
38.5 g
Protein
46-56 g
2.52 g
6.3 g
9.45 g
15.75 g
63 g
126 g
315 g
Vitamin A (Upper
Limit: 7500 mcg)
700-900 mcg
4224 mcg
10560 mcg
15840 mcg
26400 mcg
105600 mcg
211200 mcg
528000 mcg
Vitamin K (Upper
Limit: No adverse
effect)
90 -120 mcg
43.6 mcg
109 mcg
163.5 mcg
272.5 mcg
1090 mcg
2180 mcg
5450 mcg
Vitamin C
75-90 mg
0 mg
0 mg
0 mg
0 mg
0 mg
0 mg
0 mg
Vitamin E
15 mg
0.36 mg
0.9 mg
1.35 mg
2.25 mg
9 mg
18 mg
45 mg
Vitamin B1
1.1 - 1.2 mg
0.02 mg
0.05 mg
0.075 mg
0.125 mg
0.5 mg
1 mg
2.5 mg
Vitamin B2
1.1-1.3 mg
0.1812 mg
0.453 mg
0.6795 mg
1.1325 mg
4.53 mg
9.06 mg
22.65 mg
Vitamin B3
14-16 mg
0.596 mg
1.49 mg
2.235 mg
3.725 mg
14.9 mg
29.8 mg
74.5 mg
Vitamin B6
1.3-1.7 mg
0.0384 mg
0.096 mg
0.144 mg
0.24 mg
0.96 mg
1.92 mg
4.8 mg
Vitamin B12 (Upper
Limit: No adverse
effect)
2.4 -2.6 mcg
6.48 mcg
16.2 mcg
24.3 mcg
40.5 mcg
162 mcg
324 mcg
810 mcg
Biotin
30 mcg
0.2 mcg
0.5 mcg
0.75 mcg
1.25 mcg
5 mcg
10 mcg
25 mcg
Folic acid
400 mcg
0.4 mcg
1 mcg
1.5 mcg
2.5 mcg
10 mcg
20 mcg
50 mcg
Phantothenic acid
5 mg
0.004 mg
0.01 mg
0.015 mg
0.025 mg
0.1 mg
0.2 mg
0.5 mg
Inositol
Not available
2.56 mg
6.4 mg
9.6 mg
16 mg
64 mg
128 mg
320 mg
Calcium
1000-1200 mg
18.72 mg
46.8 mg
70.2 mg
117 mg
468 mg
936 mg
2340 mg
Iron
8-18 mg
3.496 mg
8.74 mg
13.11 mg
21.85 mg
87.4 mg
174.8 mg
437 mg
Phosphorus
700 mg
38.44 mg
96.1 mg
144.15 mg
240.25 mg
961 mg
1922 mg
4805 mg
Iodine
150 mcg
5.68 mcg
14.2 mcg
21.3 mcg
35.5 mcg
142 mcg
284 mcg
710 mcg
Magnesium
310-420 mg
12.76 mg
31.9 mg
47.85 mg
79.75 mg
319 mg
638 mg
1595 mg
Zinc
8-11 mg
0.058 mg
0.145 mg
0.2175 mg
0.3625 mg
1.45 mg
2.9 mg
7.25 mg
Selenium
55 mcg
(Upper Limit -
400 mcg)
1.02 mcg
2.55 mcg
3.825 mcg
6.375 mcg
25.5 mcg
51 mcg
127.5 mcg
Copper
900 mcg
18.8 mcg
47 mcg
70.5 mcg
117.5 mcg
470 mcg
940 mcg
2350 mcg
Manganese
1.8-2.3 mg
0.1304 mg
0.326 mg
0.489 mg
0.815 mg
3.26 mg
6.52 mg
16.3 mg
Boron
Not available
40 mcg
100 mcg
150 mcg
250 mcg
1000 mcg
2000 mcg
5000 mcg
Chromium
20-35 mcg
16 mcg
40 mcg
60 mcg
100 mcg
400 mcg
800 mcg
2000 mcg
Molybdenum
45 mcg
40 mcg
100 mcg
150 mcg
250 mcg
1000 mcg
2000 mcg
5000 mcg
Potassium
4.7 g
0.0664 g
0.166 g
0.249 g
0.415 g
1.66 g
3.32 g
8.3 g
Sodium
1.2-1.5 g
0.02564 g
0.0641 g
0.09615 g
0.16025 g
0.641 g
1.282 g
3.205 g
Germanium
1.5 mg /day
(Schauss 1991)
0.0024 mg
0.006 mg
0.009 mg
0.015 mg
0.06 mg
0.12 mg
0.3 mg
Cobalt
25-600 mcg
(Mucklow et al.
1990)
NA
NA
NA
NA
NA
NA
NA
Fluorene
3 - 4 mg
NA
NA
NA
NA
NA
NA
NA
J Nut Res (2015) 3(1): 62-79
67
Protein Energy Wasting (PEW)
Wasting refers to the process by which a debilitating diseases
cause‟s muscle and fat tissue to waste “away” and it is also
referred to acute malnutrition. Protein Energy Wasting (PEW):
term was coined by the “International Society of Renal Nutrition
and Metabolism (ISRNM)” to address the syndromes of muscle
wasting, malnutrition and inflammation during Chronic Kidney
Diseases (CKD) orAcute Kidney Injury (AKI) and it also means
loss of body protein mass and fuel reserves (Fouque et al. 2008).
Spirulina: PEM and PEW
The idea of using Spirulina to combat against malnutrition i.e.
hunger alleviation, was conceived in 1984 by Fox RD, in his
work on fighting against malnutrition with Spirulina with various
available technologies. He also promoted villagers to grow
Spirulina from recycled village wastes and proposed to use
Spirulina as concentrated nutritional food supplement to increase
immuno-resistance against infectious diseases (Fox 1985).
Henrikson (1989):in his book on “Earth food Spirulina”,
explained various nutritional properties, clinical studies and in
recent updated edition released in 2010, he has also included
chapters on alge for bio-fuel production and interesting recipes. S.
platensis is described as a good source of complementary diet to
prevent malnutrition in developing countries (Kim 1990). The
idea of cultivation of Spirulina or any other alternative protein
source, for reducing the incidents off hunger, starvation, and
malnutrition was suggested by Rodulfo (1990). Bucaille (1990)
studied the effectiveness of Spirulina algae as food for children
with protein-energy malnutrition. Many experiments were done
on rats to prove the renoprotective properties of Spirulina
(Table 9).
Table 4: Production of Spirulina and its social acceptance, cost effectiveness studies for hunger alleviation in developing countries
Country
Summary of Results
Subject
Reference
Chile
Mass cultivation, process optimization and economic analysis for growth of spirulina in 30
ponds (1120 m2) was carried out at Santaigo production facility, Chile
Production
Valderrama et al.
1987
India
Spirulina (Arthrospira) fusiformis was grown in small mud pots to provide food supplements
for a family has been developed and acceptability of the method as a family enterprise was
evaluated.
Production
Jeeji and
Seshadri 1988
USA
Earthrise Farms, USA tried popularizing spirulina by preparing granola bar and various kinds
of pasta
Product
development
Henrikson 1989
Vietnam
Spirulina platensis culture was bought from France to Institute of Biology, Hanoi, Vietnam. In
1977, a pilot pond of 12 m2 was started in Thuanha, Vietnam and in 1980, it is expanded to
3000 m2 and all process parameters were optimized to suite Vietnam atmosphere.
Production
Kim 1990
Bangladesh
Spiruilna cultivation in pilot plant was started by Applied Botany Section, Biological Research
Division, Bangladesh Council of Scientific and Industrial Research Laboratories
(BCSIR):Dhaka. A technology was developed to suite Bangladesh environment.
Production
(Nahar and
Begum 1991)
France
The use of Spirulina as a possible feed for aqua culture was demonstrated in the study by
growing tilapia, small pelagic fishes, shrimp, and mollusks in a series of artificial canals.
Aqua culture
Fox 1999
Kenya
Five spirulina cultivation sites were selected and the possibility for further development and
promotion were evaluated in the project. It is found that is Significant efforts need to be made
to improve the scope of production, bringing nutrition experts and NGO‟s at national level.
Production
Harris 2010
Brazil
Spirulina was proved to be an adequate protein source for recovery of body weight and muscle
protein of protein malnourished rats.
Rats
Voltarelli 2011
India
Value added extruded product with 5% Spirulina + 95% Wheat flour + 5% Corn flour was
developed and sensory parameters like taste, odour, texture, color, appearance were found to
be at acceptable level.
Product
development
Vijayarani et al.
2012
Brazil.
Different formulations of cassava cake were developed varying the concentration of
Spirulina platensis and cassava bran. Based on the sensory tests, the product received excellent
acceptance level.
Product
development
Navacchi et al.
2012
Chad
Detailed explanation about the Spirulina and its development in Chad since 1988 and
initiatives of the BIEP (Interminestrial Bureau of Studies and Programing):in collaboration
with the BECMA (Bureau of Studies and Culture of Microalgae) were outlines in this paper
along with the production technology.
Production
Halawlaw 2013
Iran
The Spirulina platensis and Chlorella vulgaris were incorporated into probiotic fermented
milks to increase the functional properties.
Product
development
Beheshtipour
2013
Indonesia
The aim of the work is to develop a product for local production of Spirulina in Indonesia and
promoting amoung uneducated Indonesian fishermen.
Production
Van Koolwijk
2014
Egypt
Sixteen food formulas were prepared for as complementary food babies (1-3 years age) by
using spirulina at 0, 2.5 0.5 and 7.5% for the production of two types of baby food one of them
is ready to eat by using some fruits and vegetables and evaluated.
Product
development
Sharoba 2014
Algeria
The product formulation composed by 2/3 of jujube syrup, 1/6 Spirulina water extract and 1/6
natural lemon juice was found to be best and further analysis of nutrients was done. The
formulation reveals satificatory microbiological quality and also allows exploration of the
Ziziphus jujuba fruit which is in extinction in Algeria.
Product
development
Benahmed et al.
2014
Arab League
Five blends were prepared with one control and other blends with varying spirulina
concentration from 2.5 to 10% and properties like taste, texture, odour, nutritional
composition, physical and functional properties and microbiological properties were
evaluated.
Product
development
Morsy et al.
2014
France
The phenomenon of social conversion by farmers from traditional agricultural systems to
Spirulina production was explained in detail along with the impact on conversion.
Production
Stéfanini 2015
India
High saline (0.4M NaCl) and low nitrogen (<0.01 M NaNO3) significantly increased the
carotenoid production in Spirulina platensis, which may be resulted due to excessive
formation of free radicals under stress.
Production
Sujatha and
Nagarajan 2013
Spain
Supercritical fluid extraction (SFE) was used to enrich Vitamin E in spirulina and 29.4 mg/g
vitamin E was achieved.
Production
Mendiola et al.
2008
68
J Nut Res (2015) 3(1): 62-79
PEM due to hunger
There are two types of hungers, one is hunger due to lack of food
and other is lack of micronutrients, “hidden hunger” (Bindu and
Channarayappa, 2014). Lack of adequate food sources in under
developing countries and lack of proper nutritional awareness in
developed countries, resulted in micronutrient deficiency and
malnutrition. The self sufficiency in some developing countries
was achieved by increasing the production of cereal crops but it
resulted in decrease in the production of pulses which are main
sources of protein (Babu and Rajasekaran 1991). This may be the
prime cause of malnutrition in developing countries.
Spirulina can be considered as a best source of protein in terms of
gram protein per cultivatable land ratio but major problem faced
in developing countries is the acceptance level of this super food
into daily recipes. Various studies from 1991 on social
acceptance of algal supplements as alternative food, cost
effectiveness in growing Spirulina in developing countries, field
and clinical studies on human population were done by many
researchers (Table 4 and Table 5) to understand and alleviate
hidden hunger and malnutrition (Babu and Rajasekaran 1991) and
provide food security. Few studies on each and every micro
nutrient were tabulated in Table 7 and Spirulina as an alternative
cheap feed for animals and aqua culture was also tabulated in
Table 8.
In 1989, Earthrise Farms, USA, tried popularizing granular bars.
Mass cultivation, process optimization and economic analysis for
growing Spirulina was done at Santaigo production facility, Chile
(Valderrama et al. 1987). In 1988, Jeeji and Seshadri tried
popularizing mud pot cultivation in India i.e. 30 to 40 L capacity
open culture vessel to produce 2 grams of Spirulina per day per
person and 3 pots are sufficient to produce enough Spirulina for a
family with 3 to 4 members. Mass production in Vietnam was
started from 1980 (Kim 1990). Pilot scale plants in 1980‟s were
started in Bangladesh by Applied Botany Section, Biological
Research Division, Bangladesh Council of Scientific and
Industrial Research Laboratories (BCSIR):Dhaka and later
extended to rural communities (Habib et al. 2008). Detailed
experimentation about Spirulina since 1988 was done by BIEP
(Interminestrial Bureau of Studies and Programing):in
collaboration with the BECMA (Bureau of Studies and Culture of
Microalgae in Chad (Halawlaw 2013). In China, Spirulina
Table 5: Clinical studies for combating malnutrition using Spirulina in developed and in under developing countries.
Country
Summary of Results
Subject
Reference
France
At the Hôpital Bichat, France, Spirulina (80-90 grams/day) was administrated to
undernourished children. Adsorption of Spirulina protein was found to be good and also
observed that in spite of heavy dosage, there is no noteworthy increase in blood uric acid.
Children
Santillan 1974
Mexico
Administration of 2 to 3 grams of protein (in terms of either Spirulina/Cow‟s milk/Soya) per
body weight for four days was given to 10 children aged 5 to 10 months and it found that the
relative retention of Spirulina is high when compared with cow‟s milk and soya.
Children
Proteus Inc.
(1975)
China
27 children aged 2-6 years old were administrated with 1.5 g Spirulina mixed with 12 g baked
barley sprout, Vitaimn B1 and Zinc. The children in a short period recovered from diarrhea
and constipation at Nanjing Children Hospital, China.
Children
Miao 1987
Democratic
Republic of
the Congo
Spirulina was administrated to 28 children suffering from protein-energy diseases. The
parameters measured during the study, showed a positive effect of Spirulina on patients.
Children
Bucaille 1990
Austria
Suggested to use C13 stable isotope as tracer to assess the impact of infection in
undernourished people and on kinetics of protein breakdown and synthesis.
Malnourished
population
IAEA (1992)
India
1 gram of dried Spirulina fusiformis was given every day as nutritional supplement to 5000
pre-school children for a period of 6 to 13 months and clinical parameters were evaluated.
Based on the survey at the end of the study, 4% reduction in incidence of Bitot's spots was
observed.
Children
Seshadri 1993
Burkina-Faso
The effectiveness of giving 5 g/day of Spirulina to 182 children for 90 days, suffering from
malnutrition does not resulted in any change in weight gain.
Children
Branger et al.
2003
Burkina-Faso
Spirulina + Misola (millet, soja, peanut) based food was given to 550 undernourished children
suffering from malnutrition at the Centre Medical St. Camille, Uagadougou, Burkina Faso.
This study confirms that Spirulina plus Misola are good food supplements for undernourished
children.
Children
Simpore et al.
2006
Brazil
Young Wistar rats (30 days old) were fed for 60 days with 17% protein from Spirulina and
compared to rats fed 17% protein casein. The body weight, length, soleus muscle total protein,
protein degradation and DNA were similar in both groups but The muscle protein synthesis
rates were increased in rats fed with Spirulina diet.
Rats
Voltarelli and de
Mello 2008
Brazil
Spirulina was proved to be an adequate protein source for recovery of body weight and muscle
protein of protein malnourished rats.
Rats
Voltarelli 2011
India
900 mg of Spirulina was administrated to 100 girls with age 11 to 13 years for 6 months and
significant improvement anthropometric measurements and hemoglobin, serum ferrtin, serum
zinc, serum protein and serum albumin levels was observed.
Children
Ramesh et al.
2013
Brazil
23 Wistar rats were given Spirulina based diet in malnutrition phase for 30 days and
significant nutrition recovery of animals was observed. The study proved that low Spirulina
percentage diet (Spirulina 8.8% + casein 5.0%) are better than high Spirulina percentage diet
(Spirulina 17.6% + casein 0.15% or Spirulina 26.4%).
Rats
Moreira et al.
2013
Zambia
60 children (18 to 36 months) were divided into two equal groups and one group was given
10 g Spirulina daily intake and other group without Spirulina intake were monitored for 9
months and the Spirulina treated children showed larger improvement in height for age Z
score.
Children
Masuda et al.
2014
India
200 adolescent girls (13-15 years):from Shimla were divided into equal groups and one group
was given 1 gram Spirulina + 40 grams wheat basan ladoo (an Indian recipe) for 6 days a
week for two months and other group was given placebo for the same period. The group with
Spirulina supplementation showed less prevalence of common ailments (paleness of skin,
conjunctiva, dental caries, fatigue) when compared with other group.
Children
Dewan 2014
J Nut Res (2015) 3(1): 62-79
69
Micronutrient
Summary of Results
Subject
Country
Reference
Vitamin A
The experiments done on rats showed that the biological values of
alga were acceptable and also established in his work that dried
spirulnia contain more β-carotene (pro-vitamin A).
Rats
France
Clement et al. 1967
Spirulina (0 to 26.7%) was fed to male rats for 6 weeks. At low levels
of Spirulina feed (<2.7) and high level (>10.7%) caused reduction in
plasma, liver and heart α-tocopherol. Liver retinoid levels decreased
when fed with >10.7% and < 10.7 % there is in increase in retinoids.
Spirulina was found to significantly alter the storage and utilization of
Vitamin A.
Rats
USA
Mitchell et al. 1990
The absorption of β-carotene in Spirulina fed rats was found to be low
when compared with rats fed with synthetic β-carotene. Spirulina fed
rats have not shown dosage related increase in Vitamin A in liver and
serum but the vitamin A storage was found to be much higher than
expected.
Rats
India
Annapurna et al.
1991
The initial loss of beta-carotene on spray drying were between 7 to
10% and on storage in colored bottles containing air, more than 50%
loss was observed in <45 days. Flakes (>20 mesh size) retain 52% and
spray dried fine powder (100 mesh) retained 34%. The authors
recommended producing dry alga in the form of flakes or granules to
retain beta carotene. Sodium metabisulphite (0.1 to 1.0%) as an
antioxidant can be used to retard degradation rate of beta carotene.
The opened containers should be exhausted within 15 days of
purchase and minimum air/oxygen access is required to retain beta-
carotene.
Storage and
loss
India
Seshadri et al 1991
Spirulina based on β - carotene level (equivalent to 60 µg/d and 120
µg/d) was fed to vitamin A depleted rats for 10 days. The Spirulina
fed group showed better growth.
Rats
India
Kapoor and Mehta
1993
Hexachlorocyclohexane (HCH) (1000 ppm) was mixed with Spirulina
(0.0628% and 3.18%) and fed to male albino rats for 7 weeks. Growth
rate reduced but body weight increased at the end of seventh week.
The ameliorating effects of alga on the dietary toxicity of HCH in
retinol deficient albino rats were established.
Rats
India
Venkataraman et al.
1994
Spirulina (30 g/Kg) was fed to female shrimps with Pigment
Deficiency Syndrome (PDS) for 4 weeks and the study confirms that
the bioavailablity of carotenoids is high and inclusion in diet to is
recommended for shrimps with precluded carotenoid deficiency
related problems.
Shrimp
India
Regunathan and
Wesley 2006
In a group of well-nourished, normal-weight Chinese men following
low-vitamin A diets, 4.5 mg Spirulina β-carotene consumed with 22 g
fat has the same Vitamin A activity as does 1 mg retinyl acetate.
Human
China
Wang et al. 2008
Neuroprotective effects of a Spirulina 0.1% supplemented diet in the
G93A SOD1 mouse model of ALS beginning at 5 weeks of age and
continuing for 10 weeks. Spirulina dietary supplement significantly
maintained body weight and extension reflex, and reduced
inflammatory markers and motor neuron degeneration in G93A mice.
Rats
USA
Garbuzova-Davis
and Bickford 2010
Spirulina (2 grams and 4 grams) was fed to 228 children (6-11 years)
for 5 days per week for 10 weeks. The total body vitamin storage
increased significantly with a median increase of 0.160 mmol in the
children taking 2 grams and 0.279 mmol for children taking 4 grams
Spirulina.
Human
China
Li et al. 2012
Vitamin B
Complex
Spirulina produce non-cobalamin Vitamin B-12 analogues that are
unavailable to humans and even block Vitamin B-12 metabolism.
Human
USA
Herbert and Drivas
1982
The bioavailability of the Vitamin B-12 in children with B12
deficiency was checked by feeding them 0.1 to 2.7 mcg Vitamin B-
12/day (Algal equivalent) for 2 months. There is an increase in plasma
vitamin B-12 level but change in Mean Corpuscular Volume (MCV)
is not significant suggesting that low bioavailablity of Vitamin B-12
from Spirulina.
Human
The
Netherlands
Dagnelie et al. 1991
No difference in body weight gain, relative liver, or relative kidney
weight could be found in male weaning Wistar rats fed with Spirulina
for four weeks. The rats were initially feed for 6 weeks, vitamin B-12
deficient diet. These data illustrate that cobalamins from algae are
indeed absorbed by the rat but distribution pattern over liver and
kidneys indicates that at least part of the cobalamins, measured by a
specific radioassay, may actually be analogues.
Rats
The
Netherlands
Van den Berg 1991
Vitamin E
Spirulina (1500 mg/kg/day) and Vitamin E (50mg/kg/day) was fed to
adult female albino rats of wistar strain weighting between 180 and
220 grams for 6 weeks. The lens soluble protein, glutathione and
water content profiles show the preventive role of Spirulina and
Vitamin E in naphthalene-induced cataract in rats.
Rats
India
Haque and Gilani
2005
70
J Nut Res (2015) 3(1): 62-79
Calcium
Novel sulfated polysaccharide (named calcium spirulan (Ca-SP)) alga
Spirulina platensis was extracted using hot water by bioactivity-
directed fractionation. The unique polysaccharide was composed of
rhamnose, ribose, mannose, fructose, galactose, xylose, glucose,
glucuronic acid, galacturonic acid, sulfate, and calcium. Ca-SP was
found to inhibit the replication of several enveloped viruses, including
Herpes simplex virus type 1, human cytomegalovirus, measles virus,
mumps virus, influenza A virus, and HIV-1.
Inhibitor
Japan
Hayashi et al. 1996
These results suggest that Ca-SP, a novel sulfated polysaccharide,
could reduce the lung metastasis of B16-BL6 melanoma cells, by
inhibiting the tumor invasion of basement membrane probably through
the prevention of the adhesion and migration of tumor cells to laminin
substrate and of the heparanase activity.
Inhibitor
Japan
Mishima et al. 1998
Ca-SP after further purification, found to contain rhamnose, 3-O-
methylrhamnose (acofriose):2,3-di-O-methylrhamnose, 3-O-
methylxylose, uronic acids, and sulfate. The backbone of Ca-SP
consisted of 1,3-linked rhamnose and 1,2-linked 3-O-methylrhamnose
units with some sulfate substitution at the 4-position. The polymer was
terminated at the nonreducing end by 2,3-di-O-methylrhamnose and 3-
O-methylxylose residues.
Inhibitor
Japan
Lee et al. 1998
Ca-SP at 20 μg/ml or less may retard the repair process of damaged
vascular endothelium through inhibition of vascular endothelial cell
proliferation by induction of a lower ability to respond to stimulation
by endogenous basic fibroblast growth factor.
Inhibitor
Japan
Kaji et al. 2002
Iron
Ingestion of daily dose of Spiruline (10 g) recommended for human
consumption by the commercial source would provide up to 1.5 to 2
mg absorbed iron.
Rats
USA
Johnson and
Shubert 1986
The absorption of iron from Spirulina was significantly lower than that
of ferrous sulphate and whole egg but significantly greater than that
from whole wheat.
Rats
India
Kapoor and Mehta
1992
Spirulina might promote the growth rate of Iron Deficiency Anemia
(IDA) rats and there was an repletion effect of Spirulina on IDA rats.
Rats
China
Jiangming et al.
1994
The pregnant and lactating rats fed with Spirulina + wheat gluten
(22% protein equivalent) showed significant higher iron storage and
hemoglobin content then casein + wheat gluten diet.
Rats
India
Kapoor and Mehta
1998
In vitro digestion/Caco-2 cell culture system was used to measure the
iron Spirulina availability. 6.5-fold increase in iron content using
Spirulina digest in comparison with meat was observed.
Iron
Availability
France
Puyfoulhoux et al.
2001
Spirulina (3 grams/day) is supplemented for 12 weeks to 40 people
with >50 years age both male and female. Increase in hemoglobin is
found after 12 weeks and increase in Complete cell count (CCC) and
indoleamine 2,3-dioxygenase (IDO) enzyme activity was observed.
Spirulina may ameliorate anemia and immunosenescence in older
subjects.
Human
(>50 years)
USA
Selmi et al. 2011
Iodine
Spirulina was grown in 10-8 to 10-4 g/l Potassium Iodide (KI) and 0.5
to 15 mg/L Selenious acid (H2SeO3) and bioaccumulation was
observed for pharmaceutical formulation purpose. The increase of
selenium and iodine accumulation is observed at maximum 13 mg/L
and 500 mg/L concentrations respectively and polynomial equation to
explain the accumulation was also developed. If iodine content in
medium is 500mg/L, then iodine concentration in biomass 2 mg/L,
total lyophilized biomass is 0.8 g/l and iodine enrichment coefficient is
0.4%.
Formulation
Russia
Mosulishvili et al.
2002
Magnesium
Mg-fortification of Spirulina does not improve Mg availability and
that crude spirulina represents an adequate source of Mg as efficient as
all bran and Banania.
Formulation
France
Planes et al 2002
Zinc
The highest bioenrichment of Spirulina platensis to Zn and Se were
371.2μg/g and 752.7μg/g under the concentration of 4mg/L Zn and
200mg/L Se was found and above that the growth speed changed.
Bio-
enrichment
China
Wang and
Songgang 1998
Spirulina extract (250 mg) plus zinc (2 mg) twice daily for 16 weeks
may be useful for the treatment of chronic arsenic poisoning with
melanosis and keratosis.
Human
Bangladesh
Misbahuddin et al.
2006
Selenium
Se-deficient rats were then repleted for 56 days with Se (75 µg/kg of
diet) supplied as sodium selenite and Selenium enriched spirulina. The
bioavailabilities of Se in retentate, as assessed by slope ratio analysis
using selenite as a reference Se, were 89 and 112% in the tissue Se
content and 106 - 133% in the glutathione peroxidase activities.
Rats
France
Cases et al. 2002
In vitro antioxidant and antiproliferative activities of selenium-
containing phycocyanin (Se-PC) purified from selenium-enriched
Spirulina platensis was investigated and the results indicated that Se-
PC exhibited stronger antioxidant activity than phycocyanin by
scavenging ABTS, DPPH, superoxide anion, and 2,2′-azobis-(2-
amidinopropane)dihydrochloride free radicals and have potential
applications in chemoprevention.
Bio-
enrichment
China
Chen and Wong
2009
J Nut Res (2015) 3(1): 62-79
71
industries are supported by State Science and Technology
Commission (SSTC) as a National Strategic Programme since
1986. The SSTC developed various technologies related to
medium optimization, downstream processing, practical use and
strain selection and there were approximately 80 factories in
China in 1997 cultivating about 106 m2 producing 400 tons
Spirulina powder per year (Li and Qi, 1997). Promotion of
Spirulina in five cultivation sites in Kenya was done by Harris
2010. A value added food products were developed by Vijayarani
et al. (2012) and Navacchi et al. (2012):India, Beheshtipour
(2013):Iran, Sharoba (2014):Egypt, Benahmed et al.
(2014):Algeria, Morsy et al. (2012):Arab League, and Van
Koolwijk (2014):Indonesia and social conversion by farmers
from traditional agro systems to Spirulina production was studied
in France (Stefanini 2015).
Spirulina proved to recover malnourished rats (Volatrelli and De
Mello 2008;Voltarelli 2011) and another study on malnourished
rats for 30 days, proved that low Spirulina diet (8.8%) is more
effective than high Spirulina diet (>17.6%). In one study,
Spirulina fed 5 g/day to malnourished children does not resulted
in any change in weight gain (Branger et al. 2003) (Table 5).
Spirulina was administered up to 90 g/day to under nourished
children at the Hôpital Bichat, France and in spite of heavy
dosage, absorption levels of proteins were found good (Santillan
1974). Spirulina was administered 2 to 3 grams per kg body
weight to 5 to 10 month‟s old children and observed that the
protein retention rate is high (Proteus Inc. 1975). 1.5 grams of
Spirulina mixed with 12 g baked barley sprout, vitamin B1 and
zinc recovered children from diarrhea and constipation (Miao
1987). Many such studies on children with protein energy
diseases (Bucaille 1990):malnutrition (Simpore et al.
2006):Vitamin A deficiency (Seshadri 1993):nutrition for healthy
children (Ramesh et al. 2013;Masuda et al. 2014;Dewan 2014)
were done along with special studies like using C13 stable isotope
along with Spirulina to understanding the kinetics of protein
breakdown (IAEA 1992). Still further studies on Spirulina are
required to establish the optimal concentration level for each
disease conditions and malnutrition. Various studies on
micronutrients and role of Spirulina in human body is listed in
Table 6.
According to IIMSAM (Intergovernmental Institution for the use
of Micro-algae Spirulina against Malnutrition):recognized by
United Nations (UN) and consultative observer of The United
Nations Economic and Social Council (ECOSOC):UN, there are
178 million globally estimated stunned children. IIMSAM works
to promote the use of Spirulina against acute malnutrition and
global food security by promoting its mandate and collaborating
with various countries (H.E. Remigio M. Maradona 2008).
Since 1967, many researchers tried establishing Spirulina as a
major source of vitamin A with highest bioavailability of beta-
carotene in rats (Clement et al. 1967; Mitchell et al. 1990;
Annapurna et al. 1991; Kapoor and Mehta 1993; Venkataraman
et al. 1994; Garbuzova-Davis and Bickford 2010):humans
(Wang et al. 2008; Li et al. 2012) and aqua culture (Regunathan
and Wesley 2006). The studies on loss of beta-carotene during
storage, spray drying and other unit operations was done by
Seshadri et al (1991). The studies for increasing the productivity
of beta-carotene by changing the medium composition of
Spirulina were also done (Sujatha and Nagarajan 2013).
Based on their studies on bioavailability of Vitamin B12 in
humans (Herbert and Drivas (1982) and Dagnelie et al. (1991)) it
is suggested not to use it as a source of vitamin B12 for children
with B12 deficiencies as it contain non-cobalamin Vitamin B-12
analogues that are unavailable to humans. Similar results were
also supported by Van den Berg (1991). Studies on Vitamin K,
were not available and studies on Vitamin E are found to be less
(Haque and Gilani 2005; Mendiola et al. 2008). Calcium spirulan
(Ca-SP)) from Spirulina platensis was isolated in Japan in 1998
and since then enormous amount of research was done on it,
against various diseases including HIV, measles virus, mumps
virus, influenza A virus, and cancer (Hayashi et al. 1996;Mishima
et al. 1998; Lee et al. 1998; Kaji et al. 2002). Research on
Spirulina as a source of iron for healthy and anemic rats were
done since 1986 (Johnson and Shubert 1986; Kapoor and Mehta
1992; Jiangming et al. 1994; Kapoor and Mehta 1998;
Puyfoulhoux et al. 2001) and aged population in 2011 (Selmi et
al. 2011) and exact bioavailability values were also established
(Table 6).
Magnesium fortification of Spirulina does not improve the
magnesium bioavailability (Planes et al 2002) but further studies
on this area are required and bioenrichment of Spirulina with
high concentrations of iodine (Mosulishvili et al. 2002):zinc and
selenium (Wang and Songgang 1998) significantly improved the
mineral concentrations. Spirulina with zinc can be used for
treatment of chronic arsenic poisoning with meelanosis and
keratosis (Misbahuddin et al. 2006). The bioavailability values of
selenium were available in Table 6 (Cases et al. 2002). Purified
selenium from Spirulina can be used as strong antioxidant and
have potential applications in chemoprevention (Chen and Wong
2009). Large corporations are required to promote research on
Spirulina for establishing exact bioavailability values of
micronutrients so that Spirulina can be used for enteral nutrition
in malnourished patients. Overall, based on the above data,
Spirulina can be used as a source for alleviating hidden hunger or
micronutrient deficiencies in children but care should also be
taken while administrating Spirulina to the patients by referring
to Table 3.
Spirulina as an alternative feed for animals and aquaculture
Spirulina as an alternative feed for animals and aqua was reported
in Table 7. Cyanobacteria as a source of food for aqua culture
were established by Fox (1999). A system including Spirulina,
Artemia and mangrove fauna was used for producing tilapia,
small pelagic fishes, shrimp, and mollusks in artificial canals with
circulating filtered sea water. Spirulina was used as a feed for
poultry, pig, cattle and many other animals and aqua culture.
Various studies on Spirulina as an alternative feed for animals
and aquaculture were listed in Table 7.
After considering the listed facts in table 6, Spirulina can be fed
up to 10 % for poultry (Ross and Dominy 1990) and less than 4%
for Quail (Ross et al. 1994). Increase in the Spirulina content up
to 40g/kg for 16 d in 21 day old boiler male chicks, resulted in
yellow and red coloration of flesh and this may be due to the
accumulation of the yellow pigment, zeaxanthin (Toyomizu et al.
2001). Pigs (Nedeva et al. 2014):rabbits (Peiretti and Meineri
2008) and lambs (Holman et al. 2012) can receive up to 10% of
the feed and increase in the Spirulina content in cattle resulted in
increase in milk yield and weight (Stanley and Jones 1976;
Kulpys et al. 2009; Heidarpour et al 2011). Spirulina as an
alternative feedstock and immune booster for various types of
fish including big mouth buffalo, (Stanley and Jones 1976):milk
fish (Santiago et al. 1989):cultured striped jack (Shigeru et al.
1991):carp (Ayyappan 1992; Ramakrishnan et al. 2008):red sea
bream (Mustafa et al. 1994):tilapia (OlveraNovoa et al.
72
J Nut Res (2015) 3(1): 62-79
Table 7: Various studies on Spirulina as an alternative feed for animals and aquaculture for alleviating hunger and for providing food security
Country
Summary of Results
Subject
Reference
USA
Bigmouth buffalo Ictiobus cyprinellus (Valenciennes):was fed with 29 g dry weight per kg body
weight Spirulina for 28 days and an increase of 14 g/Kg body weight was observed.
Big mouth
buffalo
Stanley and
Jones (1976)
French
Polynesia
Spirulina (0 to 8 %) in pelletized form was fed to shrimps. The growth, survival and pigmentation
were considerably more when compared with single cell ingredient sources like lactic yeast.
Shrimp
Cuzon et al.
1981
The
Philippines
Wild milkfish fry (90/m2):were fed with Spirulina and formulated diet. The stocking rate was
92.5/m2 after 7 weeks and the Spirulina fed fish gave weight increment (0.881±0.140 g).
Milkfish
Santiago et al.
1989
USA
Spirulina (0 to 20%) was fed to poultry and found that day old chicks, after 3 weeks, the growth rate
reduced for 10% and 20% spirulina feed and >12% diet receiving Hubbard male boiler chicks after
41 days, a slight decrease in growth was observed but there is no significant difference due to the
Spirulina and concentration level up to 10% except increase in color of yolk and fertility rate.
Poultry
Ross and
Dominy 1990
Japan
The levels of carotenoids were increased by supplementation of S. maxima 5 to 10% diet to Cultured
striped Jack Caranx delicatissimus.
Cultured
Striped
Jack
Shigeru et al.
1991
India
10% Spirulina in basal diet improved specific growth rates and live weight
Carp
Ayyappan 1992
Japan
The red sea bream were fed with 2% Spirulina for 95 days and elevated protein assimulation and
increased stromal fraction was observed.
Red sea
bream
Mustafa et al.
1994
USA
There was a consistent increase in yolk color with increase in concentration from 0% to 4% of freeze
dried spirulina in quails fed for 8 weeks. Yolk color increased more in freeze-dried Spirulina when
compared with extruded Spirulina.
Quail
Ross et al.
1994
USA
Spirulina and its potential applications as an animal feed were reviewed.
Aqua
Culture
Belay et al.
1996
South
Africa
Juvenile Haliotis midae, Port Alfred, South Africa, were fed red alga (Pfocamium corallorhiza) for 3
months before the experiment. Spirulina based diet (19% protein) was fed for 124 days along with 4
other feeds (casein, fishmeal, soya oil cake and torula yeast). fishmeal and Spirulina spp. algae are
found to be most suitable proteins for inclusion in practical diets for H. midae.
Abalone
Britz 1996
México
Spirulina (20 to 100%) diet along with animal protein was given 6% of their body weight to tilapia in
a closed recirculating system. After a 9 week feeding period, the growth rate and protein utilization
increased in 20% and 40% spirulina diet. Further increase in Spirulina, decreased the growth.
Tilapia
OlveraNovoa
et al. 1998
Italy
40 crossbred rabbits were given Spirulina platensis (5% to 15%) for 24 days and found no obvious
health problems. The final weight gain and feed efficiency did not alter significantly but rabbits
receiving >10% spirulina showed highest feed intake.
Rabbits
Peiretti and
Meineri 2008
India
Spirulina maximus at 3% diet to common carp (Cyprinus carpio - 4.59±0.95 g) produced the specific
growth rate (1.27±0.02%/d):feed conversion ratio (0.71±0.08):and , protein efficiency ratio
1.96±0.03.
Carp
Ramakrishnan
et al. 2008
Lithuania
The Lithuanian black and white cows in their early lactation period were fed with 200 g of spirulina
per day for 90 days. The cow‟s receiving Spirulina became 8.5 to 11 % fatter and gave 34 kg milk
per day in the beginning of their lactation and it is found to be 6 kg more than those of the control
group.
Cow
Kulpys et al.
2009
Taiwan
White shrimp (Litopenaeus vannamei):were given Spirulina (6 to 20 µg/g):which is earlier hot water
extracted and compared with normal spirulina (200 to 600 mg/L) for 24 to 96 hours. Shrimp that
received the hot-water extract of S. platensis had enhanced innate immunity and increased resistance
against V. alginolyticus infection.
Shrimp
Tayag et al
2010
Iran
Twenty four Holstein calves were given Spirulina platensis 0 g to 25 g per day for 57 days. The
results showed that treatment effect was not significant on the final weight, daily gain; daily feed
intake, feed efficiency and digestibility coefficient below 25 g. Increase in the level up to 25 grams,
decrease in digestibility in terms of crude protein, dry matter, neutral detergent fiber, and organic
matter were observed. However, reduction in plasma cholesterol, LDL, HDL concentration was
found and there is no effect on other blood parametters like BUN, albumin and globulin.
Holstein
calves
Heidarpour et
al 2011
Thailand
Spirulina (3% and 5%) was fed to African Sharptooth Catfish (Clarias gariepinus) with initial size
30.63-32.47 g for 60 days. The immunity (1.70 Units/mL) for 5% Spirulina feed was found to be
higher.
Catfish
Promya and
Chitmanat
2011
Turkey
Spirulina (0 to 10%) was fed to fish (3.75±0.02g) for 12 weeks. The specific growth rate, feed
intake, total egg production, hatching rate of eggs was found to be higher. The yellow and blue
coloration of the yellow tail cichlid and carotenoid in skin was enhanced.
Yellow tail
Güroy et al.
2012
Australia
24 weaned lambs (purebred Merino dams sired by Dorset, White Suffolk, Black Suffolk and
Merino rams lamb) weighing 37.5±5.2 kg, 42 days old were fed with 0 to 20 wt/vol Spirulina for 6
weeks. Lambs on Spirulina levels of 10% recorded the highest mean live weight of 41.9 ± 0.7 kg
and lambs with 20% did not significantly improve when compared to the control group (0%).
lamb
Holman et al.
2012
France
Spirulina platensis was given as a sole food for zebrafish broodstock, egg production was found to
be lower but survival rate (73%) was higher when compared with commercial feed (55%). No
difference in egg and larval weight and size was observed and the larval survival rate of 69% at 31
days post fertilization was observed. The spirulina based diet is recommended for zebrafish larvae in
the first few days of life.
Zebrafish
Geffroy 2013
Bangladesh
Studies were done on the growth performance, feed utilization and body composition of fiingerlings
of stinging cat fish and effect of spirulina.
Cat fish
Ali 2014
Bulgaria
48 Danube white pigs, weighing 12.15 to 12.471 kg were given 2 to 3 g per day for 47 days. The
weight increased to 30.9 to 33.9 kg and significant increase in growth intensity from 12.50% to
14.25% was observed. The number of erythrocytes and hemoglobin are 15% and 13 % higher in 3 g
fed pigs. There are relatively small number of sick animals (<2.40%) when compared with control
group (5.40%).
Pigs
Nedeva et al.
2014
J Nut Res (2015) 3(1): 62-79
73
1998):catfish (Promya and Chitmanat 2011; Ali 2014):yellow
tail (Güroy et al. 2012):Zebrafish (Geffroy 2013): and shrimps
(Cuzon et al. 1981; Tayag et al 2010) and Abalone (Britz 1996)
was established and up to 2% Spirulina per day in feed can be
safely recommended for fish, shrimps and abalone (Table 7).
Effect of Spirulina in combating against Protein Energy
Malnutrition (PEM) in patients with various chronic diseases
PEM in cancer patients
Protein calorie under nutrition is seen in advanced cancer patients
with loss of adipose tissue, visceral protein and skeletal muscle
varying unpredictably from patient to patient. Good nutrition may
increase the survival rate of the patients (Nixon et al. 1980).
Table 8 shows the list of clinical studies on Spirulina and its
benefits for alleviating protein energy malnutrition in cancer
patients.
Spirulina algae extract, when applied tropically for 3 times per
week for 28 weeks along with 0.1% 7,
12dimethylbenz[a]anthracene in mineral oil, removed tumors in
hamsters (Joel Schwartz 1988). This study promoted many
scientists to explore the antitumor immunotherapy potential of
Spirulina. Extensive studies including human trails (Babu et al
1995):cell lines (Konícková et al. 2014) and on rats (Zhang et al.
2001;Khan et al. 2005; Chamorro-Cevallos et al. 2008; Akao et
al. 2009 and Ismail et al. 2009) were done to prove the cancer
inhibitory properties of Spirulina.
PEM in HIV patients
After the discovery of calcium spirulan (Ca-Sp) by Hayashi et al.
(1996):extensive research has been done to inhibit the replication
of several enveloped viruses, including (human
immunodeficiency virus) HIV-1. Studies on peripheral blood
mononuclear cells (Ayehunie et al 1998) and humans (Simpore et
al 2005; Yamani et al. 2009; Azabji-Kenfack 2011) were done
along with structural modification studies on calcium spirulan
(Lee et al. 2001). Spirulina was fed up to 25 g/day to HIV
patients and considerable improvement in weight loss, anaemia,
karnofsky score, CD4 cell count was observed along with
decrease in the HIV viral load (Simpore et al 2005; Yamani et al.
2009;Azabji-Kenfack 2011) (Table 9).
Protein Energy Wasting
Protein energy wasting describes the increase of mechanisms
causing syndromes of wasting, malnutrition, inflammation, and
their interrelationships in individuals with chronic kidney disease
(CKD) or acute kidney injury (AKI) (Fouque et al. 2008). Studies
on abrupt loss of kidney function due to exposure to mercury to
the kidney and its failure in rats was studied by Fukino et al.
(1990). Spirulina was administered along with mercury to rats
which were alive up to 10 days, where the control group which
were fed only mercury died within 4 days. The study confirms the
protective effect of Spirulina against renal failures and reduction
of general renal dysfunctions. Extensive research was done on
Table 8: Various studies on Spirulina for nutrition rehabilitation patients suffering from cancer
Country
Summary of Results
Subject
Reference
USA
Spirulina algae extract along with 0.1% 7, 12dimethylbenz[a]anthracene in mineral oil when
applied tropically for 3 times per week for 28 weeks found to remove gross tumors in
Hamster. However, microscopic sections of the buccal pouch in the Spirulina fed group
showed localized areas of dysplasia and early carcinomainsitu undergoing destruction. β
carotene and mineral oil fed group of hamsters also showed considerable decrease in tumors.
Hamster
Joel Schwartz
1988
India
1g/day of Spirulina was fed to oral leukoplakia patients in Kerala, India and complete
regression of lesions was observed in 20 of 44 subjects supplemented and within one year of
discontinuing supplements, 9 out of 20 reponders within spirulina fed developed recurrent
lesions. Patients did not result in increased serum concentration of retinol or βcarotene, nor
was it associated with toxicity.
Human
Babu et al 1995
China
Spirulina platensis (12, 30 an 60 mg/kg) was administrated for 21 days to mice and dogs,
which were damaged by injecting cyclophosphamie annd 60Co- irradiation. 30 and 60 mg/kg
increased the level of white cells in blood and nucleated cells and DNA in bone marrow but no
effect in red cells in mice but 12 mg/kg increased the level of red cells, white cells and
hemoglobin in blood and nucleated cells in bone marrow in dogs. Spirulina has chemo-
protective and radio protective capabilities.
Mice and
Dog
Zhang et al. 2001
India
Spirulina was administered orally for 3 days, twice daily for 7 weeks to mouse, which were
earlier treated with doxorubicin (DOX) for 4 weeks. In vitro cytotoxic studies using ovarian
cancer cells demonstrated that Spirulina did not compromise the anti tumor activity of
doxorubicin.
Mouse
Khan et al. 2005
México
Spiruina (0 to 800mg/kg body weight) was given to mice for 2 weeks. Protective effects of
spirulina in relation to cyclophosphamide -induced genetic damage to germ cells was found.
Mice
Chamorro-
Cevallos et al.
2008
Japan
Syngeneic tumor-implant mice (C57BL/6 versus B16 melanoma) were fed with spirulina to
elucidate the mechanism of raising antitumor NK (Natural Killer) activation. Orally
administered Spirulina enhances tumoricidal NK activation through the MyD88 pathway.
Spirulina and BCGcell wall skeleton synergistically augmented IFN-γ production and
antitumor potential in the B16D8 versus C57BL/6 system. We infer from these results that NK
activation by Spirulina has some advantage in combinational use with BCGcell wall skeleton
for developing adjuvant-based antitumor immunotherapy.
Mice
Akao et al. 2009
USA
Spirulina (1%) against dibutyl nitrosamine (DBN) precursors were studied on rats (120±5g).
The study indicates that the liver tumor was reduced from 80% to 20% by Spirulina.
Immunohistochemical results show that PCNA and p53 were reduced by spirulina
supplementation. Spiruilna inhibited cell prolifeation, increased p21 and decreased the
expression levels at 48 hrs post treatment.
Rat
Ismail et al. 2009
Czech
Republic
Spirulina inhibited the pancreatic cancer growth rate since the third day of treatment. Decrease
in the generation of mitochondrial ROS and glutathione redox status was observed.
Human
pancreatic
cancer cell
lines
Konícková et al.
2014
74
J Nut Res (2015) 3(1): 62-79
rats but very few studies were available on human population
(Table 10).
Stoilov et al. (1999) proposed the idea of using 5 to 30% protein
hydrolysate from Spirulina, fish and macroronus along with
natural bee honey can be used to patients with chronic renal
insufficiency. High Spirulina diet should be avoided for patients
with renal stone deposition problems (Farooq et al. 2005).
Renoprotective potential against Gentamicin (Kuhad et al.
2006):Cisplatin (Mohan et al. 2006):ethylene glycol (Al-Attar
2010):4-nitroquinoline-1-oxide (Viswanadha et al.
2011):mercury (Rodríguez-Sánchez et al. 2012):deltamethrin
(Abdel-Daim et al. 2013) was established in rats and still human
trails are required to find the exact dosage of Spirulina. The
above summary of results, presented in the Table 9, from
various sources confirms that Spirulina can be used to combat
against protein energy wasting.
Conclusions
The present review had revealed that significant studies were
done on Spirulina to establish its potential use as a food
supplement, food additive, animal or aqua feed and to combat
against all forms of Protein Energy Malnutrition (PEM) and
Protein Energy Wasting (PEW). But many studies are required on
human population to find the exact clinical dosage of this super
food to patients with different protein-calorie or renal disease
conditions. The above review also suggests to use Spirulina not
greater than 4 grams per day for normal healthy adults, <25
Table 10: Various studies on spirulina and protein energy wasting in renal problems
Country
Summary of Results
Subject
Reference
USA
Approximately 5 to 30% protein hydrolysate prepared from protein source Spirulina, fish, and
macroronus with 70 to 95% of natural bee honey can be used to patients with chronic renal
insufficiency or other protein metabolic disorders.
Human
Stoilov et al.
1999
India
Effect of urinary oxalate and uric acid level on high spirulina diet and risk of nephrolithiasis was
found by Spirulina (1500 mg/kg and 0;75% in drinking water) for 4 weeks. The crystal deposition
and damage in renal cells was observed. During hyperoxaluric conditions the Spirulina diet must
possibly be avoided and can be considered in normal subjects checked for family history of renal
stone deposition.
Rats
Farooq et al. 2005
India
Renoprotective potential of Spirulina (500 too 1500mg/Kg) against Gentamicin (100mg/kg) was
evaluated on rats. Treatment with Spirulina significantly restored renal functions, reduced lipid
peroxidation and enhanced reduced glutathione levels, superoxide dismutase and catalase
activities.
Rats
Kuhad et al. 2006
India
Spirulina (1,000 mg/kg) was administered orally for 8 days and Cisplatin treatment was given on
day 4 and Nephrotoxicity was assessed after 6 days. There is decrease in the levels of superoxide
dismutase, catalase and glutathione peroxidase and increase in lipid peroxidation, plasma urea,
creatinine, urinary β-NAG, plasma and kidney tissue malondialdehyde. Spirulina significantly
protected the Cisplatin induced nephrotoxicity through its antioxidant properties.
Rats
Mohan et al. 2006
Saudi Arabia
Rats were fed with 0.75% ethylene glycol in drinking water for three weeks and after that they
were fed with Spirulina (20 mg/kg body weight) for another three weeks. The rats fed with
spirulina recovered from nephrolithiasis or renal stone disease and completely from hepatotoxicity
induced by ethylene glycol.
Rats
Al-Attar 2010
India
Oral pretreatment with Spirulina to rats, prevented 4-nitroquinoline-1-oxide induced hepato and
nephrotoxicity. The antioxidant properties mediated by Spirulina in eliminating reactive free
radicals were established.
Rats
Viswanadha et al.
2011
Mexico
Phycobiliproteins and C-phycocyanin extracted from Spirulina were fed to rats with mercury (5
mg/Kg Intraperitoneal). All doses of phycobiliprotein and C-phycocyanin prevented enhancement
of oxidative markers and protected against mercuric cholirde caused cellular damage in the
kidneys.
Rats
Rodríguez-
Sánchez et al.
2012
Egypt
Hepatonephroprotective and antioxidant potential of Spirulina against deltamethrin toxicity in rats
was assessed. Spirulina normalized the elevated serum levels of AST, ALT, APL, uric acid, urea
and creatinine. Furthermore, it reduced deltamethrin-induced lipid peroxidation and oxidative
stress in a dose dependent manner.
Rats
Abdel-Daim et al.
2013
Table 9: Various studies on Spirulina for nutrition rehabilitation patients suffering from HIV patients
Country
Summary of Results
Subject
Reference
USA
Spirulina (0.3 to 1.2 µg/ml):reduced viral production by approximatly 50% in peripheral
blood mononuclear cells (PBMC). Fractionation of the extract revealed antiviral activity in
the polysaccharide fraction and also in a fraction depleted of polysaccharides and tannins.
Peripheral
blood
mononuclear
cells (PBMC)
Ayehunie et al
1998
Japan
Calcium ion binding with the anionic part of the molecule was replaced with sodium and
potassium ion in Calcium Spirulan. The replacement of calcium ions with sodium and
potassium maintained the antiviral activity but divalent and trivalent metal ions decreased
the antiviral activity.
Structural
modification
Calcium
Spirulan
Lee et al. 2001
Italy
Spiurlina 15 to 25 g/day was fed to 84 children with HIV infection for 8 weeks and
compared with 86 undernourished children. Level of anaemia decreased during the study and
81.8% of undernourished children and 63.6% of HIV infected children were recuperated.
Spirulina can be effective for weight loss and anaemia for HIV and HIV negative
undernourished children.
Children
Simpore et al
2005
Central African
Republic
79 patients with HIV were given 10 grams of Spirulina per day for six months. No
difference was found in patients receiving Spirulina and the control group but there was an
increase in protidemia, creatinemia and Karnofsky score.
Human
Yamani et al.
2009
Cameroon
Food supplements, calculated as per 1.5 g/Kg body weight proteins and spirulina (25%) was
given to malnourished HIV infected adults with age 18 to 35 years for 12 weeks. HIV viral
load significantly decreased and increase in CD4 cell count was observed at the end of the
study.
Human
Azabji-Kenfack
2011
J Nut Res (2015) 3(1): 62-79
75
grams/day for HIV patients, <2 % for aqua culture and <10% for
poultry and animal feed. Exact dosage has to be developed for
cancer patients and patients with renal problems. Spirulina is not
recommended as a source of vitamin B12 for vitamin B12
deficiency children (Herbert and Drivas 1982;Dagnelie et al.
1991) and low dosage of Spirulina (5g/day) does not showed any
significant increase in weight in malnourished children (Branger
et al. 2003) and it is also not recommended for patients with
family history of renal stone depositions. Extensive studies on
Vitamin K, Vitamin B1, Vitamin B2, Vitamin B3, Vitamin B6,
improvement of cobalamin Vitamin B-12 in Spirulina strains
using genetic modification, clinical potential of calcium-spirulan
against HIV and other viral diseases, antitumor and
renoprotective properties of Spirulina on human population are
required for further understanding the clinical potential of
Spirulina to combat against PEM and PEW. Specific mechanisms
should be developed by industries to remove vitamin A, vitamin
K, vitamin B12, molybdenum and chromium to increase the
consumption level up to 100 grams of Spirulina per day.
Development of various Spirulina fortified foods are required to
create nutritional awareness and increase the acceptance level in
developing countries.
References
Abdel-Daim MM, Abuzead SMM, Halawa SM (2013) Protective
Role of Spirulina platensis against Acute Deltamethrin-
Induced Toxicity in Rats. PLoS ONE 8(9):e72991.
doi:10.1371/journal.pone.0072991
Akao Y, Ebihara T, Masuda H, Saeki, Y, Akazawa T, Hazeki K,
Seya T (2009) Enhancement of antitumor natural killer cell
activation by orally administered Spirulina extract in mice.
Cancer Sci 100(8):1494-1501.
Al-Attar AM (2010) Antilithiatic influence of Spirulina on
ethylene glycol-induced nephrolithiasis in male rats. Am J
Biochem Biotechnol 6(1):25-31.
Ali M (2014) Evaluation of the effects of feed attractants
(Spirulina and ekangi) on growth performance, feed
utilization and body composition of fingerlings of stinging
cat fish, Heteropneustes fossilis (Bloch, 1792) (Doctoral
dissertation)
Annapurna VV, Deosthale YG, Bamji MS (1991) Spirulina as a
source of vitamin A. Plant foods for human nutrition,
41(2):125-134.
Ayehunie S, Belay A, Baba TW, Ruprecht RM (1998) Inhibition
of HIV-1 Replication by an Aqueous Extract of Spirulina
platensis (Arthrospira platensis) JAIDS J Acquired Immune
Deficiency Syndromes 18(1):7-12.
Ayyappan S (1992) Potential of Spirulina as a feed supplement
for carp fry. Seshadri CV, Jeeji Bai N (eds) Spirulina
Ecology, Taxonomy, Technology, and Applications. National
Symposium, Murugappa Chettiar Research Centre, Madras
171-172.
Azabji-Kenfack M, Dikosso SE et al (2011) potential of Spirulina
Platensis as a nutritional supplement in Malnourished HIV-
Infected Adults in sub-saharan Africa: A Randomised,
single-Blind study. Nutrition Metabolic insights 4:29.
Babu Mathew, Rengaswamy Sankaranarayanan, Padmanabhan P
et al (1995) Evaluation of chemoprevention of oral cancer
with spirulina fusiformis. Nutrition and Cancer 24(2):45
Babu SC, Rajasekaran B (1991) Biotechnology for rural nutrition:
An economic evaluation of algal protein supplements in
south India. Food Policy 16(5):405-414.
Beheshtipour H, Mortazavian AM, Mohammadi R et al (2013)
Supplementation of Spirulina platensis and Chlorella vulgaris
algae into probiotic fermented milks. Comprehensive
Reviews Food Sci. Food Safety 12(2):144-154.
Belay A, Kato T, Ota Y (1996) Spirulina (Arthrospira): potential
application as an animal feed supplement. J App. Phycology
8(4-5): 303-311.
Belay A, Ota Y, Miyakawa K, Shimamatsu H (1993) Current
knowledge on potential health benefits of Spirulina. J App
Phycology 5(2): 235-241.
Benahmed Djilali A, Mahouel H, Kaci NM. et al. (2014, May).
Development of possibility of natural juice using
Ziziphusjujuba and Spirulina. In Industrial, Medical and
Environmental Applications of Microorganisms: Current
Status and Trends: Proceedings of the V International
Conference on Environmental, Industrial and Applied
Microbiology (BioMicroWorld2013) Mad (p. 272).
Wageningen Academic Publishers.
Bindu S, Channarayappa (2014) The hidden hunger and strategies
for its alleviation A review. J Nut Res 2(1):32-37
Branger B, Cadudal JL, Delobel M et al (2003). Spiruline as a
food supplement in case of infant malnutrition in Burkina-
Faso. Archives de pediatrie: organe officiel de la Societe
francaise de pediatrie, 10(5):424-431.
Britz PJ (1996). The suitability of selected protein sources for
inclusion in formulated diets for the South African abalone,
Haliotis midae. Aquaculture, 140(1):63-73.
Bucaille P (1990). Effectiveness of spirulina algae as food for
children with protein-energy malnutrition in a tropical
environment. PhD thesis, Toulouse, University Paul
Sabatier, France.
Burlew JS (1953). Algal culture. From Laboratory to Pilot Plant,
Carnegie Inst. Washington Publ, 600(1).
Cases J, Wysocka IA, Caporiccio B et al (2002). Assessment of
selenium bioavailability from high-selenium spirulina
subfractions in selenium-deficient rats. J Agricultural Food
Chemistry 50(13):3867-3873.
Chamorro-Cevallos G, Garduno-Siciliano L, Barron BL et al
(2008). Chemoprotective effect of Spirulina (Arthrospira)
against cyclophosphamide-induced mutagenicity in mice.
Food Chemical Toxic. 46(2):567-574.
Chen T, Wong YS (2008). In vitro antioxidant and
antiproliferative activities of selenium-containing
phycocyanin from selenium-enriched Spirulina platensis. J
Agri.Food Chemistry 56(12):4352-4358.
Clement G, Giddey C, Menzi R (1967). Amino acid composition
and nutritive value of the alga Spirulina maxima. J Sci. Food
Agri. 18(11):497-501.
Cuzon, G., Santos, R. D., Hew, M., & Poullaouec, G. (1981). Use
of Spirulina in Shrimp (Penaeus japonicus) diet. J World
Mariculture Society 12(2):282-291.
Dagnelie PC, van Staveren WA, van den Berg H (1991). Vitamin
B-12 from algae appears not to be bioavailable. American J
Clin. Nut. 53(3):695-697.
De Onis M, Monteiro C, Akré J, Clugston G (1993) The
worldwide magnitude of protein-energy malnutrition: an
overview from the WHO Global Database on Child Growth.
Bulletin of the World health Organization, 71(6):703-712.
Dewan A (2014) Impact of Spirulina as a Nutritional Supplement
on the Dietary Intake and Health Status of Adolescent Girls
of Shimla. J Res.: THE BEDE ATHENAEUM, 5(1):26-34.
Dietary Reference Intakes (DRIs): Recommended Intakes for
Individuals (PDF):(2004) Food and Nutrition Board, Institute
of Medicine, National Academies, USA 2004.
Dillon JC (1999) The young child nutrition and malnutrition. In
7th World Congress on Clinical Nutrition , 14-16 October
1999, New Delhi, India.
76
J Nut Res (2015) 3(1): 62-79
Dinesh Kumar R, Manikandavelu D, Guru Kasirajan K (2010)
Fixation of Carbon dioxide and oxygen production by
photosynthetic simulations in indoor environs, J Algal
Biomass Utln 1(4): 84-88
Fairfield KM, Fletcher RH (2002) Vitamins for chronic disease
prevention in adults: scientific review. Jama, 287(23):3116-
3126.
Falquet J (1997) The nutritional aspects of Spirulina. Antenna
Technology, Switzerland
Falquet J (2000) A sustainable response to malnutrition in hot
regions: the local production of spirulina, Geneva, Antenna
Technologies, 2000.
Farooq SM, Ebrahim AS, Asokan D et al (2005) Credentials of
Spirulina diet on stability and flux related properties on the
biomineralization process during oxalate mediated renal
calcification in rats. Clin. Nut. 24(6):932-942.
Fouque D, Kalantar-Zadeh K, Kopple J et al (2008) A proposed
nomenclature and diagnostic criteria for proteinenergy
wasting in acute and chronic kidney disease. Kidney
International, 73(4):391-398.
Fox RD (1984) Fighting Malnutrition with Spirulina Appropriate
Technology for the Third World. Worldview, I1 June.
Washington. I) c.
Fox RD (1985) Spirulina: The Alga That Can End Malnutrition.
Futurist, 19(1):30-35.
Fox RD (1999) Third millenium aquaculture. Farming the micro-
oceans. Bulletin de l'Institut océanographique, 547-563.
Fukino, H., Takagi, Y., & Yamane, Y. (1990) Effect of Spirulina
(S. platensis) on the Renal Toxicity Induced by Inorganic
Mercury and Cisplatin (Regular Presentations)(Proceedings
of the 15 th Symposium on Environmental Pollutants and
Toxicology) 衛生化学, 36(1)
Garbuzova-Davis S, Bickford PC (2010) Short communication:
neuroprotective effect of Spirulina in a mouse model of ALS.
Open Tissue Engineering and Regenerative Medicine J 3:36-
41.
Geffroy B (2013) Effects of a Spirulina platensis-based diet on
zebrafish female reproductive performance and larval
survival rate. Cybium, 37(1-2):31-38.
Gershwin ME, Belay A (Eds.) (2007) Spirulina in human
nutrition and health. CRC Press, USA
Gopalan C (1998) Micronutrient malnutrition in SAARC-the
need for a food-based approach. NFI BULLETIN, 19, 1-4.
Grover Z, Ee LC (2009) Protein energy malnutrition. Pediatric
Clinics of North America, 56(5):1055-1068.
Güroy B, Şahin İ, Mantoğlu S, Kayalı S (2012) Spirulina as a
natural carotenoid source on growth, pigmentation and
reproductive performance of yellow tail cichlid
Pseudotropheus acei. Aquaculture International, 20(5):869-
878.
HE Remigio M Maradona (2008):Presentation to IIMSAM US
Senate-Congress, 23-25, July 2008, Washington D.C., USA.
http://iimsam.org/images/presentation_to_congress_23_25_j
uly08.pdf
Habib MAB, Parvin M, Huntington TC, Hasan MR (2008) A
review on culture, production and use of spirulina as food for
humans and feeds for domestic animals and fish. Food And
Agriculture Organization of The United Nations.
Halawlaw YI (2013) Methodology of North-South Technology
Transfer. The Case of the Development of
Spirulina.International J Emerging Tech Adv Eng 3(6):42-58
Haque SE, Gilani KM (2005) Effect of ambroxol, Spirulina and
vitamin-E in naphthalene induced cataract in female rats.
Indian J. Physiol. Pharmacol, 49(1):57-64.
Harris KN (2010) The Prospects of Using Athrospira platensis as
a Malnutrition Treatment in Kenya.
Hayashi T, Hayashi K, Maeda M, Kojima I (1996) Calcium
spirulan, an inhibitor of enveloped virus replication, from a
blue-green alga Spirulina platensis. Journal of Natural
Products, 59(1):83-87.
Heidarpour A, Fourouzandeh-Shahraki AD, Eghbalsaied S (2011)
Effects of Spirulina platensis on performance, digestibility
and serum biochemical parameters of Holstein calves.
African Journal of Agricultural Research, 6(22):5061-5065.
Henrikson R (1989) Earth food spirulina. Laguna Beach, CA:
Ronore Enterprises, Inc.
Henrikson R (1994) Microalga Spirulina, superalimento del
futuro. Ronore Enterprises. 2• ed. Ediciones Urano,
Barcelona, España. 222 p.
Herbert V, Drivas G (1982) Spirulina and vitamin B12. JAMA,
248(23):3096-3097.
Hoffman JR, Falvo MJ (2004) Proteinwhich is best?. Journal of
sports science & medicine, 3(3):118.
Holman BWB, Kashani A, Malau-Aduli AEO (2012) Growth and
body conformation responses of genetically divergent
Australian sheep to Spirulina (Arthrospira platensis)
supplementation. American Journal of Experimental
Agriculture, 2(2):160-173.
Ismail MF, Ali DA, Fernando A et al (2009) Chemoprevention of
rat liver toxicity and carcinogenesis by Spirulina.
International journal of biological sciences, 5(4):377.
Jeeji Bai N, Seshadri CV (1988) Small scale culture of Spirulina
(Arthrospira) as a food supplement for rural households -
Technology development and transfer. Algological
Studies/Archiv für Hydrobiologie, 50-53:565 - 572
Jiangming L, Kaiguo W, Chuanzhen M et al (1994) Repletion
effect of spirulina on iron deficiency anemia in rats [j]. Acta
nutrimenta sinica, 4.
Joel Schwartz, Gerald Shklar , Susan Reid, Diane Trickier (1988)
Prevention of experimental oral cancer by extracts of
SpirulinaDunaliella algae. Nutrition and Cancer 11(2):127-
134.
Johnson PE, Shubert LE (1986) Availability of iron to rats from
spirulina, a blue-green alga. Nutrition Research, 6(1):85-94.
Kaji T, Fujiwara Y, Inomata Y, Hamada C, et al (2002) Repair of
wounded monolayers of cultured bovine aortic endothelial
cells is inhibited by calcium spirulan, a novel sulfated
polysaccharide isolated from Spirulina platensis. Life
sciences, 70(16):1841-1848.
Kapoor, R. A. S. H. M. I., & Mehta, U. (1992) Iron
bioavailability from Spirulina platensis, whole egg and whole
wheat. Indian journal of experimental biology, 30(10):904-
907.
Kapoor R, Mehta U (1993) Utilization of β-carotene from
Spirulina platensis by rats. Plant foods for human nutrition,
43(1):1-7.
Kapoor R, Mehta U (1998) Supplementary effect of spirulina on
hematological status of rats during pregnancy and lactation.
Plant Foods for Human Nutrition, 52(4):315-324.
Khan M, Shobha JC, Mohan IK et al (2005) Protective effect of
Spirulina against doxorubicininduced cardiotoxicity.
Phytotherapy Research, 19(12):1030-1037.
Kim DD (1990) Outdoor mass culture of Spirulina platensis in
Vietnam. Journal of Applied Phycology, 2(2):179-181.
Konícková R, Vanková K, Vaníková J et al (2014) Anti-cancer
effects of blue-green alga Spirulina platensis, a natural source
of bilirubin-like tetrapyrrolic compounds. Ann. Hepatol, 13,
273-283.
Krishnakumari MK, Ramesh HP, Venkataraman LV. (1981)
Food safety evaluation: acute oral and dermal effects of the
algae Scenedesmus acutus and Spirulina platensis on albino
rats. Journal of Food Protection®, 44(12):934-935.
J Nut Res (2015) 3(1): 62-79
77
Kuhad A, Tirkey N, Pilkhwal S, Chopra K (2006) Effect of
Spirulina, a blue green algae, on gentamicininduced
oxidative stress and renal dysfunction in rats. Fundamental &
clinical pharmacology, 20(2):121-128.
Kulpys J, Paulauskas E, Pilipavicius V, Stankevicius R (2009)
Influence of cyanobacteria Arthrospira (Spirulina) platensis
biomass additive towards the body condition of lactation
cows and biochemical milk indexes. Agron. Res, 7, 823-835.
Laliberte G, Olguín EJ, de la Noüe J (1997) Mass cultivation and
wastewater treatment using Spirulina. In A.
Lee JB, Hayashi T, Hayashi K et al (1998) Further purification
and structural analysis of calcium spirulan from Spirulina
platensis. Journal of natural products, 61(9):1101-1104.
Lee JB, Srisomporn P, Hayashi K, Tanaka T et al (2001) Effects
of structural modification of calcium spirulan, a sulfated
polysaccharide from Spirulina platensis, on antiviral activity.
Chemical and pharmaceutical bulletin, 49(1):108-110.
Li DM, Qi YZ (1997) Spirulina industry in China: Present status
and future prospects. Journal of applied Phycology, 9(1):25-
28.
Li L, Zhao X, Wang J, Muzhingi T et al (2012) Spirulina can
increase total-body vitamin A stores of Chinese school-age
children as determined by a paired isotope dilution technique.
Journal of nutritional science, 1, e19.
Masuda K, Inoue Y, Inoue R et al (2014) Spirulina Effectiveness
Study on Child Malnutrition in Zambia. Institute of
Development Studies, Brighton BN1 9RE, UK.
McCarty MF (2007) Clinical potential of Spirulina as a source of
phycocyanobilin. Journal of medicinal food, 10(4):566-570.
Mendiola JA, García-Martínez D, Rupérez FJ et al (2008)
Enrichment of vitamin E from Spirulina platensis microalga
by SFE. The Journal of Supercritical Fluids, 43(3):484-489.
Miao Jian Ren (1987):“Spirulina in Jiangxi China”. Academy of
Agricultural Science. Presented at Soc. Appl. Algology, Lille
France Sep. 1987
Misbahuddin M, Maidul Islam AZM, Khandker S et al (2006)
Efficacy of spirulina extract plus zinc in patients of chronic
arsenic poisoning: a randomized placebo-controlled study.
Clinical Toxicology, 44(2):135-141.
Mishima T, Murata J, Toyoshima M et al (1998) Inhibition of
tumor invasion and metastasis by calciumspirulan (Ca-SP):a
novel sulfated polysaccharide derived from a blue-green
alga, Spirulina platensis. Clinical & experimental metastasis,
16(6):541-550.
Mitchell GV, Grundel E, Jenkins M, Blakely SR (1990) Effects
of graded dietary levels of Spirulina maxima on vitamins A
and E in male rats. The Journal of nutrition, 120(10):1235-
1240.
Modestine KSM, Muhamadu N, Ekoe T, Inocent G (2015) Effect
of Spirulina platensis Supplementation on Nutritional and
Biochemical Parameters of Under Five Years Malnourished
Children from an Orphanage in Douala, Cameroon. Journal
of Pharmacy and Nutrition Sciences, 5(1):5-13.
Mohan IK, Khan M, Shobha JC et al (2006) Protection against
cisplatin-induced nephrotoxicity by Spirulina in rats. Cancer
chemotherapy and pharmacology, 58(6):802-808
Molitor H, Robinson HJ (1940) Oral and parenteral toxicity of
vitamin K1, phthiocol and 2 methyl 1, 4, naphthoquinone.
Experimental Biology and Medicine, 43(1):125-128.
Moorhead K, Capelli B, Cysewski GR (2011) Spirulina: Nature's
Superfood, Cyanotech Corporation, USA
Morsy OMAM, Sharoba AI EL-Desouky, HEM Bahlol, EM
Mawla (2014): "Production and evaluation of extruded food
products by using spirulina algae." Annals of Agric. Sci.,
Moshtohor ISSN 1110-0419 Vol. 52(4) 329342
Mosulishvili LM, Kirkesali EI, Belokobylsky AI et al (2002)
Experimental substantiation of the possibility of developing
selenium-and iodine-containing pharmaceuticals based on
bluegreen algae Spirulina platensis. Journal of
pharmaceutical and biomedical analysis, 30(1):87-97
Mucklow ES, Griffin SJ, Delves HT, Suchak B (1990) Cobalt
poisoning in a 6-year-old. The Lancet, 335(8695):981.
Mustafa MG, Umino T, Nakagawa H (1994) The effect of
Spirulina feeding on muscle protein deposition in red sea
bream, Pagrus major. Journal of applied ichthyology,
10(23):141-145.
Nahar L, Begum S (1991) Spirulina and its culture in Bangladesh.
In International Botanical Conference, Dhaka
(Bangladesh):10-12 Jun 1991. BBS.
Naidu KA, Sarada R, Manoj G et al (1999) Toxicity assessment
of phycocyanin-A blue colorant from blue green alga
Spirulina platensis. Food Biotechnology, 13(1):51-66.
Narasimha DLR, Venkataraman GS, Duggal SK, Eggum BO
(1982) Nutritional quality of the blue-green alga Spirulina
platensis geitler. J. Sci. Food Agric., 33: 456460.
Navacchi MFP, de Carvalho JCM, Takeuchi KP, Danesi EDG
(2012) Development of cassava cake enriched with its own
bran and Spirulina platensis-doi: 10.4025/actascitechnol.
v34i4. 10687. Acta Scientiarum. Technology, 34(4):465-472.
Nedeva R, Yordanova G, Kistanova E et al (2014) Effect of the
addition of Spirulina platensis on the productivity and some
blood parameters on growing pigs. Bulgarian Journal of
Agricultural Science (Bulgaria)
Nixon DW, Heymsfield SB, Cohen AE et al (1980) Protein-
calorie undernutrition in hospitalized cancer patients. The
American journal of medicine, 68(5):683-690.
Nowak DJ, Hoehn R, Crane DE (2007) Oxygen production by
urban trees in the United States. Arboriculture and Urban
Forestry, 33(3):220.
Ohira Y, Obata E, Kuga Y, Ando K (1998) Effect of light
intensity on respiration rate of Spirulina platensis. Kagaku
Kogaku Ronbunshu, 24(4):562-567.
OlveraNovoa MA, DominguezCen LJ, OliveraCastillo L,
MartínezPalacios CA (1998) Effect of the use of the
microalga Spirulina maxima as fish meal replacement in
diets for tilapia, Oreochromis mossambicus (Peters):fry.
Aquaculture research, 29(10):709-715.
Otten J, Hellwig J, Meyers L, eds. Dietary Reference Intakes: The
Essential Guide to Nutrient Requirements. Washington,
DC:National Academies Press; 2006
Peiretti PG, Meineri G (2008) Effects of diets with increasing
levels of Spirulina platensis on the performance and apparent
digestibility in growing rabbits. Livestock Science,
118(1):173-177.
Peiretti PG, Meineri G (2008) Effects of diets with increasing
levels of Spirulina platensis on the performance and apparent
digestibility in growing rabbits. Livestock Science,
118(1):173-177.
Planes P, Rouanet JM, Laurent C, Baccou JC, Besançon P,
Caporiccio B (2002) Magnesium bioavailability from
magnesium-fortified spirulina in cultured human intestinal
Caco-2 cells. Food chemistry, 77(2):213-218.
Promya J, Chitmanat C (2011) The effects of Spirulina platensis
and Cladophora algae on the growth performance, meat
quality and immunity stimulating capacity of the African
sharptooth catfish (Clarias gariepinus) Int J Agric Biol, 13,
77-82.
Proteus Inc. (1975) Clinical experimentation with Spirulina.
National Institute of Nutrition, Mexico City, 1975.
(Translated by Proteus, Inc.)
78
J Nut Res (2015) 3(1): 62-79
Puyfoulhoux G, Rouanet JM, Besançon P et al (2001) Iron
availability from iron-fortified spirulina by an in vitro
digestion/Caco-2 cell culture model. Journal of agricultural
and food chemistry, 49(3):1625-1629.
Ramakrishnan CM, Haniffa MA, Manohar M et al (2008) Effects
of probiotics and spirulina on survival and growth of juvenile
common carp (Cyprinus carpio) The Israeli Journal of
Aquaculture Bamidgeh 60(2):128-133.
Ramesh S, Manivasgam M, Sethupathy S, Shantha K (2013)
Effect of Spirulina on Anthropometry and Bio-Chemical
Parameters in School Children. IOSR Journal of Dental and
Medical Sciences, 7(5):11-15.
Regunathan C, Wesley SG (2006) Pigment deficiency correction
in shrimp broodstock using Spirulina as a carotenoid source.
Aquaculture Nutrition, 12(6):425-432.
Richmond A (Ed.) (2008) Handbook of microalgal culture:
biotechnology and applied phycology. John Wiley & Sons.
Rodríguez-Sánchez, R, Ortiz-Butrón R, Blas-Valdivia V,
Hernández-García A, Cano-Europa E (2012)
Phycobiliproteins or C-phycocyanin of Arthrospira
(Spirulina) maxima protect against HgCl 2-caused oxidative
stress and renal damage. Food chemistry, 135(4):2359-2365.
Rodulfo BR (1990) Culture and utilization of freshwater algae as
protein source.
Ross E, Dominy W (1990) The nutritional value of dehydrated,
blue-green algae (spirulina plantensis) for poultry. Poultry
Science, 69(5):794-800.
Ross E, Dominy W (1990) The nutritional value of dehydrated,
blue-green algae (spirulina plantensis) for poultry. Poultry
Science, 69(5):794-800.
Ross E, Puapong DP, Cepeda FP, Patterson PH (1994)
Comparison of freeze-dried and extruded Spirulina platensis
as yolk pigmenting agents. Poultry science, 73(8):1282-1289.
Rym BD (2012) Photosynthetic Behavior of Microalgae in
Response to Environmental Factors. Applied Photosynthesis,
23-46.
Sánchez M, Bernal-Castillo J, Rozo C, Rodríguez I (2003)
Spirulina (arthrospira): an edible microorganism: a review.
Universitas Scientiarum, 8(1):7-24.
Santiago CB, Pantastico JB, Baldia SF, Reyes OS (1989)
Milkfish (Chanos chanos) fingerling production in freshwater
ponds with the use of natural and artificial feeds.
Aquaculture, 77(4):307-318.
Santillan C (1974) Cultivation of the Spirulina for Human
Consumption and for Animal Feed. In International
Congress of Food Science and Technology.
Schauss AG (1991) Nephrotoxicity in humans by the ultratrace
element germanium. Renal failure, 13(1):1-4.
Selmi C, Leung PS, Fischer L et al (2011) The effects of
Spirulina on anemia and immune function in senior citizens.
Cellular & molecular immunology, 8(3):248-254.
Seshadri CV (1993):“Large scale nutritional supplementation
with Spirulina alga.” All India Coordinated Project on
Spirulina. Shri Amm Murugappa Chettiar Research Center
(MCRC) Madras, India
Seshadri CV, Umesh BV, Manoharan R (1991) Beta-carotene
studies in Spirulina. Bioresource technology, 38(2):111-113.
Sharoba AM (2014) Nutritional value of spirulina and its use in
the preparation of some complementary baby food formulas.
Journal of Food and Dairy Sci., Mansoura Univ, 5(4):517-
538.
Shigeru Okada, Wen-Liang Liao, Tetsu Mori et al (1991)
Pigmentation of Cultured Striped Jack Reared on Diets
Supplemented with the Blue-Green Alga Spirulina maxima.
NIPPON SUISAN GAKKAISHI, 57(7): 1403-1406.
Simpore J, Kabore F, Zongo F, et al (2006) Nutrition
rehabilitation of undernourished children utilizing Spiruline
and Misola. Nutr J, 5(3)7
Simpore J, Zongo F, Kabore F et al (2005) Nutrition
rehabilitation of HIV-infected and HIV-negative
undernourished children utilizing spirulina. Annals of
nutrition and metabolism, 49(6):373-380.
Stanier RY, Van Niel Y (1962) The concept of a bacterium. Arch
Mikrobiol, 42:17-35.
Stanley JG, Jones JB (1976) Feeding algae to fish. Aquaculture,
7(3):219-223.
Stéfanini P, Ravatua-Smith S (2015) The phenomenon of social
conversion among farmers in France: From traditional
agriculture to the Spirulina superfood. African Sociological
Review/Revue Africaine de Sociologie, 17(2):43-54.
Stoilov IL, Georgiev TD, Taskov MV, Koleva ID (1999) U.S.
Patent No. 5,935,605. Washington, DC: U.S. Patent and
Trademark Office.
Sujatha K, Nagarajan P (2013) Optimization of growth conditions
for carotenoid production from Spirulina platensis (Geitler)
Int J Curr Microbiol Appl Sci, 2, 325-328.
Tayag CM, Lin YC, Li CC, Liou CH, Chen JC. (2010)
Administration of the hot-water extract of Spirulina platensis
enhanced the immune response of white shrimp Litopenaeus
vannamei and its resistance against Vibrio alginolyticus. Fish
& shellfish immunology, 28(5):764-773.
Toyomizu M, Sato K, Taroda H, Kato T, Akiba Y (2001) Effects
of dietary Spirulina on meat colour in muscle of broiler
chickens. British Poultry Science, 42(2):197-202.
Valderrama G, Cardenas A, Markovits A (1987) On the
economics of Spirulina production in Chile with details on
drag-board mixing in shallow ponds. In Twelfth International
Seaweed Symposium (pp. 71-74) Springer Netherlands.
Van den Berg H, Brandsen L, Sinkeldam BJ (1991) Vitamin B-12
content and bioavailability of spirulina and nori in rats. The
Journal of Nutritional Biochemistry, 2(6):314-318.
Van Koolwijk TRS (2014) Using microorganisms to fight
malnutrition in Indonesia (Doctoral dissertation, TU Delft,
Delft University of Technology, Indonesia)
Venkataraman LV, Suvarnalatha G, Krishnakumari MK, Joseph
P (1994) Spirulίna platensis as Retinol Supplement for
Protection Against Hexachlorocyclohexane Toxicity in Rats.
Journal of Food Science and Technology, 31(5):430-432.
Vijayarani D, Ponnalaghu S, Rajathivya J (2012) Development of
Value Added Extruded Product Using Spirulina.
International Journal of Health Sciences and Research,
2(4):42-47.
Viswanadha VP, Sivan S, Shenoi RR (2011) Protective effect of
Spirulina against 4-nitroquinoline-1-oxide induced toxicity.
Molecular biology reports, 38(1):309-317.
Voltarelli FA, de Mello MAR (2008) Spirulina enhanced the
skeletal muscle protein in growing rats. European journal of
nutrition, 47(7):393-400.
Voltarelli FA, Araújo MA, Moura LP et al. (2011) Nutrition
recovery with spirulina diet improves body growth and
muscle protein of protein-restricted rats. Int J Nutr Metab, 3,
22-30.
Vonshak A (1990). Recent advances in microalgal biotechnology.
Biotech. Adv., 8: 709727.
Wang CBZHY, Songgang W (1998) Study on Bioenrichment
Selenium and Zinc by Spirulina platensis [J]. FOOD AND
FERMENTATION INDUSTRIES, 6.
Wang J, Wang Y, Wang Z et al (2008) Vitamin A equivalence of
spirulina β-carotene in Chinese adults as assessed by using a
stable-isotope reference method. The American journal of
clinical nutrition, 87(6):1730-1737.
J Nut Res (2015) 3(1): 62-79
79
Yamani E, Kaba-Mebri J, Mouala C et al (2009) Use of spirulina
supplement for nutritional management of HIV-infected
patients: study in Bangui, Central African Republic.
Medecine tropicale: revue du Corps de sante colonial,
69(1):66-70.
Yin JZ, Li Y, Zhou JY (2009) Impact Evaluation of Participatory
Nutrition Education Intervention Among School Children in
Poor Rural Area of Xiangyun County. Chinese J. School
Health 2:11.
Zhang HQ, Lin AP, Sun Y, Deng YM. (2001) Chemo-and radio-
protective effects of polysaccharide of Spirulina platensis on
hemopoietic system of mice and dogs. Acta Pharmacologica
Sinica, 22(12):1121-1124.
... It is well known that A. platensis contains a high amount of calcium, which can vary from 60 to 1,000 mg per 100 g (Guldas & Irkin, 2010;Gutiérrez-Salmeán et al., 2015;Siva Kiran et al., 2015), depending on the supplier. The recommended dietary allowance (RDA) for calcium is 1,000 mg/day for adults, 800 mg/day for children (4-8 years old), and ...
Article
Abstract Arthrospira platensis is a microalgae generally known as a source of bioactive compounds and protein. The aim of this study is to evaluate the nutritional value, sensory characteristics, and antioxidant activity of traditional kefir by addition of A. platensis. In the study, the traditional kefir samples were prepared by the addition of A. platensis at 0.05%, 0.1%, 0.5%, 1%, and 2% (w/v) by considering generally recommended daily intake rate and consumer's acceptability. The sensory analysis scores showed that kefir with 0.05% and 0.1% A. platensis have the highest score, in which case the protein in the kefir slightly increased from 27 to 37 mg/ml. The addition of 1% A. platensis to kefir was found to increase amino acid contents. Some slight differences in calcium content were observed; however, there was a fourfold increase in iron. Palmitic and oleic acids (28.94% and 19.04%) were the most abundant fatty acids. The result indicated that A. platensis addition increased the antioxidant activities (FRAP and DPPH) of kefir, and addition of traditional kefir by A. platensis is a suitable way to increase the nutritional value of kefir.
Article
Full-text available
Immunosuppressive drugs are essential for systemic lupus erythematosus (SLE) treatment, but there are concerns about their toxicity. In this study, Arthrospira platensis was used as a resource for screening of the SLE-related bioactive compounds. To discover the potential compounds, a total of 833 compounds of A. platensis C1 were retrieved from the Spirulina-Proteome Repository (SpirPro) database and by literature mining. We retrieved structures and bioassays of these compounds from PubChem database; and collected approved and potential drugs for SLE treatment from DrugBank and other databases. The result demonstrated that cytidine, desthiobiotin, agmatine, and anthranilic acid, from the alga, has Tanimoto matching scores of 100% with the following drugs: β-arabinosylcytosine/cytarabine, d-dethiobiotin, agmatine, and anthranilic acid, respectively. The bioassay matching and disease-gene-drug-compound network analysis, using VisANT 4.0 and Cytoscape, revealed 471 SLE-related genes. Among the SLE-related genes, MDM2, TP53, and JAK2 were identified as targets of cytarabine, while PPARG and IL1B were identified as targets of d-dethiobiotin. Binding affinity between the drug ligands and the algal bioactive compound ligands with their corresponding receptors were similarly comparable scores and stable, examined by molecular docking and molecular dynamic simulations, respectively.
Article
Full-text available
During the Mesolithic in Europe, there is widespread evidence for an increase in exploitation of aquatic resources. In contrast, the subsequent Neolithic is characterised by the spread of farming, land ownership, and full sedentism, which lead to the perception of marine resources subsequently representing marginal or famine food or being abandoned altogether even at the furthermost coastal limits of Europe. Here, we examine biomarkers extracted from human dental calculus, using sequential thermal desorption- and pyrolysis-GCMS, to report direct evidence for widespread consumption of seaweed and submerged aquatic and freshwater plants across Europe. Notably, evidence of consumption of these resources extends through the Neolithic transition to farming and into the Early Middle Ages, suggesting that these resources, now rarely eaten in Europe, only became marginal much more recently. Understanding ancient foodstuffs is crucial to reconstructing the past, while a better knowledge of local, forgotten resources is likewise important today.
Article
Full-text available
Spirulina, a kind of blue-green algae, is one of the Earth’s oldest known forms of life. Spirulina grows best in very alkaline environments, although it may flourish across a wide variety of pH values. There are several techniques for growing Spirulina spp., ranging from open systems such as ponds and lakes, which are vulnerable to contamination by animals and extraterrestrial species, to closed systems such as photovoltaic reactors, which are not. Most contaminated toxins come from other toxic algae species that become mixed up during harvest, necessitating the study of spirulina production processes at home. Lighting, temperature, inoculation volume, stirring speed, dissolved particles, pH, water quality, and overall micronutrient richness are only a few of the environmental parameters influencing spirulina production. This review article covers the conditions required for spirulina cultivation, as well as a number of crucial factors that influence its growth and development while it is being grown. In addition, the article discusses harvesting processes, biomass measurement methods, the identification of dangerous algae, and the risk of contaminating algae as it grows on cultures. Spirulina’s rising prospects as food for human consumption are a direct outcome of its prospective health and therapeutic advantages.
Article
Full-text available
Spirulina is a kind of blue-green algae (BGA) that is multicellular, filamentous, and prokaryotic. It is also known as a cyanobacterium. It is classified within the phylum known as blue-green algae. Despite the fact that it includes a high concentration of nutrients, such as proteins, vitamins, minerals, and fatty acids—in particular, the necessary omega-3 fatty acids and omega-6 fatty acids—the percentage of total fat and cholesterol that can be found in these algae is substantially lower when compared to other food sources. This is the case even if the percentage of total fat that can be found in these algae is also significantly lower. In addition to this, spirulina has a high concentration of bioactive compounds, such as phenols, phycocyanin pigment, and polysaccharides, which all take part in a number of biological activities, such as antioxidant and anti-inflammatory activity. As a result of this, spirulina has found its way into the formulation of a great number of medicinal foods, functional foods, and nutritional supplements. Therefore, this article makes an effort to shed light on spirulina, its nutritional value as a result of its chemical composition, and its applications to some food product formulations, such as dairy products, snacks, cookies, and pasta, that are necessary at an industrial level in the food industry all over the world. In addition, this article supports the idea of incorporating it into the food sector, both from a nutritional and health perspective, as it offers numerous advantages.
Article
Full-text available
The effects of various concentrations of iron, zinc, and manganese on Arthrospira platensis MGH-1 growth and the capability of this cyanobacterium to accumulate these micronutrients were investigated. Maximum growth parameters were exhibited by A. platensis MGH-1 at 0.1 g L⁻¹ iron, 2.0 mg L⁻¹ zinc, and 6.0 mg L⁻¹ manganese. The maximum bioaccumulation value was observed in 0.3 g L⁻¹ iron, 8.0 mg L⁻¹ zinc, and 40 mg L⁻¹ manganese. The selection of the appropriate concentration for each micronutrient to produce A. platensis MGH-1 fortified with iron, zinc, and manganese was performed based on both the parameters of growth and accumulation of these metals. Then, the effects of selected concentrations for each micronutrient were investigated on photosynthetic pigments, protein and sugar contents, antioxidant enzyme activity, phenolic compound, and fatty acid content in A. platensis MGH-1. Maximum soluble sugar, phenolic compounds, and palmitoleic acid content were exhibited at 0.1 g L⁻¹ iron. The highest amount of antioxidant enzyme activity and palmitic acid content was detected at 4.0 mg L⁻¹ zinc-treated A. platensis MGH-1. The chlorophyll-a content increased significantly at 25 mg L⁻¹ of manganese. Arthrospira platensis MGH-1 treated with the micronutrients contained high amounts of γ-linolenic acid (GLA, 18:3n-6) compared to the control. Overall, this study showed that 0.1 g L⁻¹ iron and 25 mg L⁻¹ manganese were appropriate concentrations of micronutrients to enrich A. platensis MGH-1 and it can be suggested for the development of functional foods. Also, A. platensis MGH-1 fortified with 0.1 g L⁻¹ iron has more potential to be used in nutraceutical/ functional food since it is very rich in bioactive compounds.
Article
Full-text available
Global food systems face the challenge of providing healthy and adequate nutrition through sustainable means, which is exacerbated by climate change and increasing protein demand by the world’s growing population. Recent advances in novel food production technologies demonstrate potential solutions for improving the sustainability of food systems. Yet, diet-level comparisons are lacking and are needed to fully understand the environmental impacts of incorporating novel foods in diets. Here we estimate the possible reductions in global warming potential, water use and land use by replacing animal-source foods with novel or plant-based foods in European diets. Using a linear programming model, we optimized omnivore, vegan and novel food diets for minimum environmental impacts with nutrition and feasible consumption constraints. Replacing animal-source foods in current diets with novel foods reduced all environmental impacts by over 80% and still met nutrition and feasible consumption constraints. The environmental impacts of more sustainable diets vary across regions. Using linear optimization, this study compares the reductions of global warming potential, water use and land use associated with the replacement of animal-sourced foods with novel or plant-based foods in European diets. Three diet types were considered to meet nutritional adequacy and consumption constraints.
Article
Full-text available
The cyanobacterium Arthrospira platensis, spirulina, is a source of pigments such as phycobiliprotein, phycocyanin. Phycocyanin is used in the food, cosmetic, and pharmaceutical industries because of its antioxidant, anti-inflammatory, and anticancer properties. The different steps involved in extraction and purification of this protein can alter the final properties. In this review, the stability of phycocyanin (pH, temperature, and light) is discussed, considering the physicochemical parameters of kinetic modeling. The optimal working pH range for phycocyanin is between 5.5 and 6.0 and it remains stable up to 45 °C; however, exposure to relatively high temperatures or acidic pH decreases its half-life and increases the degradation kinetic constant. Phycobiliproteins are sensitive to light and preservatives such as mono- and di-saccharides, citric acid, or sodium chloride appear to be effective stabilizing agents. Encapsulation within nano- or micro-structured materials such as nanofibers, microparticles, or nanoparticles, can also preserve or enhance its stability.
Conference Paper
Plant based milk clotting peptidases are becoming a prominent sector in dairy and allied food industries because of its higher acceptability, low cost down streaming, less labor-intensive and broad availability. The present study analyzed the potentiality of jackfruit (Arthocarpushetrophyllus), pumpkin (Cucurbita moschata)and lotus (Nelumbonucifera) seed extract for the availability of milk coagulating peptidase. The study reported that all the seed extracts has satisfactory milk curdling activity over the temperature range of (30°C - 60°C) with minimum calcium ion (0.02 M) addition. Results has shown the milk gel formation after employing jackfruit, pumpkin and lotus seed extracts
Book
Full-text available
Spirulina are multicellular and filamentous blue-green microalgae belonging to two separate genera Spirulina and Arthrospira and consists of about 15 species. Of these, Arthrospira platensis is the most common and widely available spirulina and most of the published research and public health decision refers to this specific species. It grows in water, can be harvested and processed easily and has significantly high macro- and micronutrient contents. In many countries of Africa, it is used as human food as an important source of protein and is collected from natural water, dried and eaten. It has gained considerable popularity in the human health food industry and in many countries of Asia it is used as protein supplement and as human health food. Spirulina has been used as a complementary dietary ingredient of feed for poultry and increasingly as a protein and vitamin supplement to aquafeeds. Spirulina appears to have considerable potential for development, especially as a small-scale crop for nutritional enhancement, livelihood development and environmental mitigation. FAO fisheries statistics (FishStat) hint at the growing importance of this product. Production in China was first recorded at 19 080 tonnes in 2003 and rose sharply to 41 570 tonnes in 2004, worth around US7.6millionsandUS7.6 millions and US16.6 millions, respectively. However, there are no apparent figures for production in the rest of the world. This suggests that despite the widespread publicity about spirulina and its benefits, it has not yet received the serious consideration it deserves as a potentially key crop in coastal and alkaline areas where traditional agriculture struggles, especially under the increasing influence of salination and water shortages. There is therefore a role for both national governments – as well as intergovernmental organizations – to re-evaluate the potential of spirulina to fulfill both their own food security needs as well as a tool for their overseas development and emergency response efforts. International organization(s) working with spirulina should consider preparing a practical guide to small-scale spirulina production that could be used as a basis for extension and development methodologies. This small-scale production should be orientated towards: (i) providing nutritional supplements for widespread use in rural and urban communities where the staple diet is poor or inadequate; (ii) allowing diversification from traditional crops in cases where land or water resources are limited; (iii) an integrated solution for waste water treatment, small-scale aquaculture production and other livestock feed supplement; and (iv) as a short- and medium-term solution to emergency situations where a sustainable supply of high protein/high vitamin foodstuffs is required. A second need is a better monitoring of global spirulina production and product flows. The current FishStat entry which only includes China is obviously inadequate and the reason why other countries are not included investigated. Furthermore, it would be beneficial if production was disaggregated into different scales of development, e.g. intensive, semi-intensive and extensive. This would allow a better understanding of the different participants involved and assist efforts to combine experience and knowledge for both the further development of spirulina production technologies and their replication in the field. A third need is to develop clear guidelines on food safety aspects of spirulina so that human health risks can be managed during production and processing. Finally, it would be useful to have some form of web-based resource that allows the compilation of scientifically robust information and statistics for public access. There are already a number of spirulina-related websites (e.g. www.spirulina.com, www.spirulinasource.com) – whilst useful resources, they lack the independent scientific credibility that is required.
Article
Full-text available
The algae Scenedesmus acutus and Spirulina platensis have been considered for use as a supplementary protein in feed and food. This Institute has developed the technology of production and utilization of such algae. It is essential to demonstrate their safety in view of their public health aspects, the interest of the producers and image of these new sources of foods. Both these algae, when in pure form and administered to rats orally up to the dosage of 800 mg/kg of body weight, did not exert any toxic action. No alterations were found in either body or organ weights in the treated animals. The vital organs showed normal histology. Application of both algae onto the skin of albino rats, up to 2000 mg/kg of body weight, did not elicit any skin allergy. All the animals were normal.
Article
Full-text available
Spirulina is a photosynthetic, filamentous, helical-shaped, multicellular and green-blue microalga. The two most important species of which are Spirulina maxima and Spirulina platensis. For these microórgarusms cell division occurs by binary fission. Since this material contains chlorophyll a, Jike higher plants, botanists classify it as a microalgae belonging to Cyanophyceae class; but according to bacteriologists it is a bacteria dueto its prokaryotic structure. Before Columbus, Mexicans (Aztecs) exploited this microorganism as human food; presently, African tribes (Kanembu) use it for the same purpose. Its chemical composition includes proteins (55%-70%), carbohydrates (15%-25%), essential fatty acids (18%), vitamins, minerals and pigments like carotenes, chlorophyll a and phycocyanin. The last one is used in food and cosmetic industries. Spirulina is considered as an excellent food, lacking toxicity and having corrective properties against viral attacks, anemia, tumor growth and malnUtrition. It has been reported in literature that the use of these microalgae as animal food supplement implies enhancement of the yellow coloration of skin and eggs yo !k in poultry and flaDlÍOgos, growth acceleration, sexual maturation and increase of fertility in cattle.
Article
Full-text available
Carotenoid production by Spirulina platensis was enhanced under different stress conditions such as higher salinity and nitrogen starvation. Exposure of S. platensis to high saline levels and low levels of nitrogen caused an immediate cessation of growth and a decrease in biomass. The carotenoids and B-carotene content was found to be increased at high saline levels and nitrogen starvation.The increase in -carotene content in starved cells may be attributed to excessive formation of free radicals under the stress, produced in order to protect the cells and to continue their growth.
Article
Full-text available
A 45-day feeding trial was conducted to investigate the effects of probiotics and spirulina on survival, growth, feed conversion ratio (FCR), protein efficiency ratio (PER), and total heterotrophic microbial count in common carp (Cyprinus carpio). Two probiotic organisms (the bacteria Lactobacillus acidophilus and the yeast Saccharomyces cerevisiae) and a single cell protein (Spirulina maximus) were incorporated into diets at concentrations of 1%, 2%, or 3%. The control diet contained no supplement. Spirulina maximus at 3% produced the best and statistically significant (p<0.05) survival, growth (3.69 ± 0.10 g), specific growth rate (1.27 ± 0.020/o/d), FCR (0.71 ± 0.08), and PER (1.96 ± 0.03). In general, L. acidophilus produced better growth than S. cerevisiae. The highest FCR (1.93 ± 0.05) was obtained in the control. The total heterotrophic microbial count was highest in S. cerevisiae treatments, followed by L. acidophilus and S. maximus. The present investigation shows that incorporation of a probiotic or spirulina in diets for common carp results in increased growth rate.
Article
Micronutrient deficiencies are aptly called as hidden hunger as they do not cause any immediate disorder symptoms but do cause serious health issues eventually. The situation of malnourishment is grim as it involves significant numbers of people especially women and children from various parts of the world. Micronutrient deficiency is usually due to the lack of a balanced diet and awareness on nutritional requirements. Another lesser known culprit is natural antinutritional factors present in plant based foods which reduce the bioavailablility of micronutrients causing deficiencies. This problem can easily be overcome by countermeasures like food fortification with micronutrients or by adopting suitable food processing methods like soaking, steeping, germination, cooking or fermentation. Biotechnology can also come handy here in the form of developing food crops with reduced antinutritional factors thereby enhancing micronutrient availability. Thus developing well researched & tailored micronutrient malnutrition management strategies & their effective implementation is a need of the hour. Key words: Micronutrients, Antinutritional factors, Hidden hunger, Malnutrition, Micronutrient malnutrition
Technical Report
Spirulina are multicellular and filamentous blue-green microalgae belonging to two separate genera Spirulina and Arthrospira and consists of about 15 species. Of these, Arthrospira platensis is the most common and widely available spirulina and most of the published research and public health decision refers to this specific species. It grows in water, can be harvested and processed easily and has significantly high macro- and micronutrient contents. In many countries of Africa, it is used as human food as an important source of protein and is collected from natural water, dried and eaten. It has gained considerable popularity in the human health food industry and in many countries of Asia it is used as protein supplement and as human health food. Spirulina has been used as a complementary dietary ingredient of feed for poultry and increasingly as a protein and vitamin supplement to aquafeeds. Spirulina appears to have considerable potential for development, especially as a small-scale crop for nutritional enhancement, livelihood development and environmental mitigation. FAO fisheries statistics (FishStat) hint at the growing importance of this product. Production in China was first recorded at 19 080 tonnes in 2003 and rose sharply to 41 570 tonnes in 2004, worth around US7.6millionsandUS7.6 millions and US16.6 millions, respectively. However, there are no apparent figures for production in the rest of the world. This suggests that despite the widespread publicity about spirulina and its benefits, it has not yet received the serious consideration it deserves as a potentially key crop in coastal and alkaline areas where traditional agriculture struggles, especially under the increasing influence of salination and water shortages. There is therefore a role for both national governments – as well as intergovernmental organizations – to re-evaluate the potential of spirulina to fulfill both their own food security needs as well as a tool for their overseas development and emergency response efforts. International organization(s) working with spirulina should consider preparing a practical guide to small-scale spirulina production that could be used as a basis for extension and development methodologies. This small-scale production should be orientated towards: (i) providing nutritional supplements for widespread use in rural and urban communities where the staple diet is poor or inadequate; (ii) allowing diversification from traditional crops in cases where land or water resources are limited; (iii) an integrated solution for waste water treatment, small-scale aquaculture production and other livestock feed supplement; and (iv) as a short- and medium-term solution to emergency situations where a sustainable supply of high protein/high vitamin foodstuffs is required. A second need is a better monitoring of global spirulina production and product flows. The current FishStat entry which only includes China is obviously inadequate and the reason why other countries are not included investigated. Furthermore, it would be beneficial if production was disaggregated into different scales of development, e.g. intensive, semi-intensive and extensive. This would allow a better understanding of the different participants involved and assist efforts to combine experience and knowledge for both the further development of spirulina production technologies and their replication in the field. A third need is to develop clear guidelines on food safety aspects of spirulina so that human health risks can be managed during production and processing. Finally, it would be useful to have some form of web-based resource that allows the compilation of scientifically robust information and statistics for public access. There are already a number of spirulina-related websites (e.g. www.spirulina.com, www.spirulinasource.com) – whilst useful resources, they lack the independent scientific credibility that is required.
Article
A scientific-economic experiment with a total number of 48 Danube White pigs, divided into 3 groups of 16 pigs each, spread into 8 pig pens in two repetitions was carried out at the Agricultural institute-Shumen. The experiment was started with 12.15-12.471 kg live weight and finished with 30.9-33.9 kg. The experiment period was 47 days. The aim of the present study was to investigate the effect of the addition of Spirulina platensis on the productivity, some blood parameters and health status on growing pigs. The addition of microalgae Spirulina platensis (2 and 3 g/capita daily) in the compound feed of growing pigs (from 12.15-12.471kg to 30.9-33.9 kg live weight) from Danube White breed, significantly (p≤0.05) increases the growth intensity with 12.50% and 14.25% and reduces the compound feed conversion and nutrients. The addition of Spirulina platensis effects insignificantly on the hemopoiesis stimulation-the number of erythrocytes and hemoglobin are higher with 15% and 13% respectively in animals fed with 3 g/capita daily microalgae. There is a tendency of small number of sick animals (2.40% and 2.13%) fed with Spirulina platensis compared with those in the control group (5.40%). © 2014, National Centre for Agrarian Sciences. All rights reserved.
Article
The acute and chronic toxicity of Phthiocol, 2-methyl-1,4-naphthoquinone and vitamin K1 was studied in mice, rats, and chicks. The oral L.D. 50 in mice was found to be approximately 0.2 g per kg for Phthiocol and 0.5 g per kg for 2-methyl-1,4-naphtho-quinone; no lethal effect could be produced by doses up to 25 g per kg of vitamin K1. In the chronic experiments in rats, daily feeding over a period of 30 consecutive days of 0.35 g per kg of Phthiocol, and 0.5 g per kg of 2-methyl-1,4-naphthoquinone was toxic; doses of 0.1 g per kg of Phthiocol and 0.35 g per kg of 2-methyl-1,4-naphthoquinone produced a marked fall of the erythrocyte count and hemoglobin. No such effects were observed following vitamin K1 administration. In the abdominal cavity of animals sacrificed 10 days after an intraperitoneal injection of vitamin K1 considerable amounts of an oily suspension could be observed, indicating an extremely slow rate of absorption of vitamin K1.