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Role of pigeon pea (Cajanus cajan L.) in human nutrition and health: A review

Authors:
  • NIN Indian Council of Medical Research
  • National Institute of Nutrition Indian Council of Medical Research

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Legumes and cereals are good, relatively inexpensive, sources of proteins and energy for third world countries, including India. India is a major pulse producing country, sharing 36 and 28% of total area and production of these crops. Pigeon pea (Cajanus cajan L.) is widely consumed in the form of dhal as an economical source of protein. It is a dense source of nutrients, but its nutritional elements are masked by some anti-nutritional factors decreased by different processing methods. The non-nutritive compounds of pigeon pea have been investigated for their role in the enhancement of the antioxidant and anti carcinogenic effects. Recent evidences suggest that pigeon pea bioactive compounds play a vital role in modulating the gut micribiota hence, can reduce inflammation. The Prebiotic potential of non digestible raffinose family oligosaccharides has also been investigated in animal models. Research on pigeon pea prebiotic oligosaccharide and health benefits is scanty and some research regarding this novel approach remains inconclusive and there is still much to be studied. This review article focuses on the nutritional, anti-nutritional factors bioactive compounds and other health benefits of pigeon pea.
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*Corresponding author’s e-mail: dr_devindra@rediffmail.com
Asian J. Dairy & Food Res, 37(3) 2018: 212-220
Print ISSN:0971-4456 / Online ISSN:0976-0563
Role of pigeon pea (Cajanus cajan L.) in human nutrition and health: A review
Aruna Talari and Devindra Shakappa*
Department of Dietetics,
National Institute of Nutrition (ICMR), Hyderabad-500 007, Telangana, India.
Received: 08-06-2018 Accepted: 06-09-2018 DOI: 10.18805/ajdfr.DR-1379
ABSTRACT
Legumes and cereals are good, relatively inexpensive, sources of proteins and energy for third world countries, including
India. India is a major pulse producing country, sharing 36 and 28% of total area and production of these crops. Pigeon pea
(Cajanus cajan L.) is widely consumed in the form of dhal as an economical source of protein. It is a dense source of
nutrients, but its nutritional elements are masked by some anti-nutritional factors decreased by different processing methods.
The non-nutritive compounds of pigeon pea have been investigated for their role in the enhancement of the antioxidant and
anti carcinogenic effects. Recent evidences suggest that pigeon pea bioactive compounds play a vital role in modulating
the gut micribiota hence, can reduce inflammation. The Prebiotic potential of non digestible raffinose family oligosaccharides
has also been investigated in animal models. Research on pigeon pea prebiotic oligosaccharide and health benefits is scanty
and some research regarding this novel approach remains inconclusive and there is still much to be studied. This review article
focuses on the nutritional, anti-nutritional factors bioactive compounds and other health benefits of pigeon pea.
Key words: Anti-nutrients, Oligosaccharides, Pigeon pea, Prebiotics.
Abbreviations
IYP International year of pulses
RFO Raffinose family oligosaccharides
PUFA Poly unsaturated fatty acids
RDI Recommended daily intake
HDL High density lipoprotein
LDL Low density lipoprotein
NHANES National Health and Nutrition Exami na tion Survey
LPO Lipid peroxidation
CSA Cajaninstillbene acid
TNF -α Tumor necrosis factor alpha
IL- 1β Interleukin 1 beta
SCD Sickle cell disease
AIN American Institute of Nutrition
LPO Lipid Peroxidation
Food legumes are of major importance in the human
diet contributing as the major source of vegetable protein.
Nowadays, pulses are gaining much interest in the area of
functional foods. The 68th UN General Assembly announced
2016 as the International Year of Pulses (IYP). The IYP 2016
aims at public awareness of the nutritional benefits of pulses
and towards the food security and nutrition (International
Year of Pulses 2016).
India ranks high in the production of pulses. Pigeon
pea, chickpea, black gram, green gram, lentils and peas are
major pulses consumed. Among legumes, pigeon pea is
predominantly grown and consumed in India. It is also known
as red gram, arhar, tur dal belonging to the family of Legumi
nosae. Pigeon pea was long considered to be one of the two
species of the genus Cajanus DC. The cultivation of the
pigeon pea dates back to at least 3,500 years and is assumed
that eastern part of peninsular India is the center of origin
(Van der Maeson 1995).
Pigeon pea is accepted in many parts of the world
since it is very much resistant to drought (ICRISAT). Pigeon
pea seeds compliment cereals such as corn, maize, wheat
and rice. It forms a good portion of the human diet in many
African, Asian and South American countries as well. Pigeon
pea is the economical source of protein, carbohydrate,
minerals and vitamins such as B-complex particularly in the
vegetarian diet. Along with the cereals pigeon pea provide
well balanced diet and can be comparable to other dense
protein sources like whey and soy (Akporhonor et al. 2006).
Besides its nutritional value, pigeon pea also
possesses various medicinal properties due to the presence
of a number of polyphenols and flavonoids (Singh 2016).
The nutritional components of pigeon pea are considered
crucial for human nutrition, and it is evident from several
studies that consumption of pigeon pea is associated with a
lower risk of several diseases (Singh and Basu 2012).
In India, red gram is mostly consumed in the form
of dhal (decorticated split cotyledons), after cooking in water,
to the desirable degree of softness and immature green seeds
are used as vegetable. Nowadays pigeon pea is incorporated
into food products like biscuits, noodles, pasta, sausages as
a novel ingredient for nutritional purposes, owing to its high
fibre and protein content, gluten-free status, low glycemic
Volume 37 Issue 3 (September 2018) 213
Table1: Proximate composition of pigeon pea (g/100g).
Proximate Oke, (2014) Eltayeb et al. (2010) Olalekan & Bosede, (2010) Adamu, (2013) Kunyunga et al. (2013)
Moisture 11.20 8.0 8.45±0.95 0.24 11.27±0.04
protein 22.40 21.0 24.46±0.32 30.53 17.95±0.06
fat 2.74 1.7 4.78±0.22 3.68 2.77±0.57
Carbohydrate 48.19 63.6 56.63±0.48 50.08 57.45±0.04
Fibre 7.25 2.5 1.10±0.10 5.54 6.98±0.08
Ash 8.22 3.2 4.58±0.40 9.93 3.58±0.21
index, antioxidant levels, as well as functional properties
like fat absorption and water binding capacity (Keshav 2015).
Till date several authors have reviewed the
nutritional quality and health benefits of pigeon pea in
relation to its bioactive compounds. This narrative review
article is aimed at reviewing the recent advances in research
carried out till date for the purposes of evaluation of
nutritional quality and health benefits of newly cultivated
pigeon pea including its novel prebiotic potential. The
updated findings on the effect of pigeon pea consumption in
animals and human health are summerized.
Nutritional composition of pigeon pea
Proximate composition: The proximate compositions such
as moisture, protein, fat, carbohydrate, ash and dietary fiber
of pigeon pea is shown in Table 1 (Oke 2014., Eltayeb et al.
2010., Olalekan and Bosede 2010., Adamu and Oyetunde
2013., Kunyanga et al. 2013). The pigeon pea seed is made
up of 85% cotyledon, 14% seed coat, and about 1% embryo.
It is a rich source of protein, carbohydrates, minerals and
vitamins. It’s protein content ranges between 20-22% CHO
between 51.4 – 58.8%, Crude fibre between 1.2 – 8.1% and
lipid between 0.6 – 3.8% (Faris 1990).
Carbohydrates: The starch and non-starch are the major
constituents of carbohydrates of pigeon pea consisting of
significant amount of α-galactosides. Different carbohydrate
fractions of pigeon pea are (i) available carbohydrates which
are digested in the small intestine and (ii) unavailable
carbohydrates like oligosaccharides, resistant starch, non-
cellulosic polysaccharides, pectins, hemicelluloses, and
cellulose, which are not digested in the small intestine
(Cummings 2007).
The available and unavailable carbohydrate content
of pigeon pea is summarized in Table 2 (Jairo et al. 1991.,
Mulimani and Devindra 1998., Apata 2008., Devindra et al.
2012). The unavailable carbohydrates of pigeon pea like
fructans and raffinose family oligosaccharides (RFOs) are
the major water soluble carbohydrates which adversely affect
bioavailability of certain vital nutrients.
Glycemic carbohydrate: Carbohydrates which provide
glucose for metabolism is referred to as ‘glycaemic
carbohydrate’, whereas carbohydrates that reaches the large
intestine prior to being metabolized, are called as ‘non-
glycaemic carbohydrate’. Most of the available carbo-
hydrates, some oligosaccharides and rapidly digested
starches may be classified as a glycaemic carbohydrate
(Cummings 2007).
In a study cooked legumes including pigeon pea,
chickpea, black gram, mung bean and white bean were tested
for blood glucose response among healthy human subjects.
The glycemic response to pigeon pea was 30.99 (Panlasigui
2009). Recently Devindra et al. (2016) have reported the
lower glycemic index of pigeon pea among the commonly
consumed legumes tested.
Amino acid profile: Generally the sulphur containing amino
acids (methionine and cystine) are limiting in pulses. The
amino acid profile of pigeon peas is summarized in Table 3
Table 2: Available and unavailable carbohydrate content of pigeon pea (g/100g*).
Type of CHO Jairo et al. (1991) Mulimani & Devindra (1998) Apata (2008) Devindra et al. (2012)
Available CHO
(Oligosaccharide)
Raffinose 0.77 0.62 0.5 1.42±0.03
Stachyose 2.37 1.06 2.90 1.75±0.04
Verbascose 0.43 4.00 4.95±0.28
Reducing sugars 1.20 0.52 0.91±0.01
Glucose 0.14
Fructose 0.40
Sucrose 4.02 1.16 2.01 2.32±0.07
Total soluble 6.64 6.18±0.03
Unavailable CHO
Non-cellulosic 14.00
Polysaccharides
Cellulose 9.84
Lignin 3.40
214 ASIAN JOURNAL OF DAIRY AND FOOD RESEARCH
Table 3: Amino acid profiles of pigeon pea.
Amino acid Akande et al.,(2010) Nwokolo,(1987) Kunyanga et al., , Ade-Omowaye et al.
(g/ 16gN) (g/ 100g) (2013) (g/ 100g) (2015) (g/ kg)
Lysine 7.79 7.4 0.25- 14.77
Histidine 3.66 5.0 0.66 7.93
Arginine 5.86 6.9 1.11 13.51
Aspartic acid 11.56 9.9 1.84 22.55
Threonine 3.12 3.7 0.72 8.25
Serine 3.59 4.9 0.99 1.42
Glutamic acid 9.23 19.7 3.14 43.31
Proline 3.17 4.8 0.85 1.44
Glycine 3.07 4.2 0.69 7.85
Alanine 3.79 4.6 0.91 9.72
Cystine 1.19 0.8 0.24 5.47
Valine 5.85 4.4 1.09 8.67
Methionine 1.19 1.1 0.23 2.65
Isoleucine 3.47 3.7 0.64 7.71
Leucine 6.78 7.8 1.38 16.48
Tyrosine 2.63 2.9 0.47 5.52
Phenylalanine 6.15 8.9 1.69 22.19
Tryptophan ND 0.15 ——
(Nwokolo 1987., Akande et al. 2010., Ade-Omowaye et al.
2015., Longvah et al. 2017). Pigeon pea seeds contain high
amounts of lysine, leucine, aspartic acid, glutamic acid and
arginine and provide essential amino acids when consumed
with cereals and other sulphur containing amino acids (Ade-
Omowaye et al. 2015). In a study Pigeon pea can replace
soybean without adversely affecting the performance of
rabbits (Adamu and Oyetunde 2013).
Fatty Acid Profile: The major saturated fatty acid in pigeon
pea is the palmitic acid which constitutes 15-25% in the
neutral lipids, 20-40% in the glycolipids, and 26-30% in the
phospholipids. The fatty acid profile of pigeon pea is
summarized in Table 4. A study was conducted to know the
nutritional potential of nine underexploited legumes in
Southwest Nigeria. The most abundant polyunsaturated fatty
acid (PUFA) identified in pigeon pea was linoleic acid
(C18:2) (Ade-Omowaye et al., 2015).
Caprylic, lauric, oleic and eicosanoic acids were
present only in small quantities. The resistant starch derived
from processed red gram showed a higher amount of short
chain fatty acids. Whereas Indian food composition tables
reported the palmitic acid content of pigeon pea as 236 ±
11.0, oleic acid was 78.55± 6.71, stearic acid was 40.95±
3.31 mg/100g respectively (Longvah et al. 2017).
Vitamin and mineral content: Pigeon pea is a good source
of water soluble vitamins, like thiamine, riboflavin, niacin
etc. Vitamin content of pigeon pea is summarized in Table 5.
Pigeon pea was reported to be the richest vegetable for
Vitamin C with 569 mg/100g. Its content was three times
higher than for peppers and could cover more than 949% of
the recommended daily intake (RDI) of Vitamin C and pigeon
pea was found to have high carotenoid content with 364.3
µg/100g when compared to other pulses (Ellong et al., 2015).
Whereas Indian food composition tables reported the thiamin
content of pigeon pea as 0.74 , riboflavin 0.15, niacin, panto
thenic acid 1.56, total B6 0.42,biotin 0.65, total folates 229
mg/ 100g respectively (Longvah et al., 2017).There are limi
ted studies on the lutein and zeaxanthin levels in pigeon pea.
Pigeon pea is a good source of minerals such as
phosphorus, magnesium, iron, calcium, sulphur and
potassium but low in sodium (Kunyanga et al. 2013). Mineral
content of pigeon pea is summarized in Table 6. Sangle,
(2015) have reported minerals constituents of two viable
mutant varieties of pigeon pea. Mean content of nitrogen
ranged from 1.95%- 3.33% and 2.24% - 3.17%, calcium
content ranged from 0.25% - 0.37% and 0.26% - 0.51% and
phosphorus content of viable mutants ranged from 0.56 % -
0.72 % and 0.58% - 0.80% in varieties of pigeon pea
respectively (Sangle, 2015).Whereas Indian food
composition tables reported the calcium content of pigeon
pea as 1.39, copper 1.32, iron 5.37 mg/100g respectively
(Longvah et al. 2017).
Anti-nutritional factors: Like other legume seeds Pigeon
pea seeds also contain some anti-nutritional factors including
phytolectins, polyphenols (phenols and tannins) and enzyme
inhibitors (trypsin, chymotrypsin, and amylase). Different anti-
nutritional factors of pigeon pea are summarized in Table 7
(Harris et al. 2014., Nwaogu and Emejulu 2010., Nwosu et
al. 2013., Balogun 2013., Aja et al. 2015a). These anti-
nutritional factors can be reduced by different processing
methods like chemical soaking (Devindra and Aruna 2016).
Germination was found to be the best method for decreasing
the phytic acid content of pigeon pea. Application of
gamma irradiation can be used as an effective method of
preservation of pigeon pea flour and their products
(Bamidele and Akanbi 2013).
Volume 37 Issue 3 (September 2018) 215
Table 5: Vitamin content of pigeon pea (mg/100g).
Vitamins Longvah et al., (2017) Faris et al., (1987) Kanyunga et al., (2013) Singh et al., (2016)
(mg/100g) (mg /g) (mg /g) (mg/g)
Β-Carotene 0.05±0.03 0.6
Thiamin (V-B1) 0.74±0.028 0.40 0.72±0.08 0.18
Riboflavin (V-B2) 0.15±0.015 0.17 0.14±0.33 2.9
Niacin 2.42±0.18 2.20 2.90±0.10
Ascorbic acid (V-C) NA 4.80±0.00
Pantothenic acid 1.56±0.13 0.68 1.26
Pyridoxine 0.07 0.28
Tocopherol (γ+α) 0.39
Folic acid * (µg/100g) 173 100.00 456
Total folate 229±19.0
Table 6: Mineral composition of pigeon pea.
Minerals Longvah et al. Olaleken & Bosede Nwokolo (1987) Kunyanga et al., (2013)
(mg/100g) (2017) (mg/g) (2010) (mg/kg) (mg/100g)
Calcium 1.39±11.8 0.65±0.03 1500 80.50±1.22
Magnesium 1.55±0.01 1410 108.00±0.02
Copper 1.32±0.15 0.56±0.03 18
Iron 5.37±1.36 0.36±0.03 39 5.60±1.41
Zinc 2.3 1.54±0.10 24 2.70±0.00
Sodium 0.33±0.00
Phosphorous 55.00±0.20 2450 334.00±0.00
Potassium 12500
Table 4: Fatty acid profile of pigeon pea (g/kg).
Name of Nwokolo, (1987) Kunyunga et al. (2013) Ade –Omovaye et al. Longvah et al. (2017)
Fatty acid (g/100g) (g/100g) (2015) (g/kg) (mg/100g)
Capric acid (10:0) 2.45
Lauric acid (12:0) 18.56
Myristic acid (14:0) 23.73 0.30
Palmiticacid(16:0) 10.98 26.2±0.00 21.59 236.00±11.0
Stearic acid (18:00) 3.32 4.0±0.01 5.88 40.95±3.31
Oleic acid (18:1) 8.44 9.2±0.01 10.21 78.55±6.71
Linoleic acid (18:2) 22.54 53.7±0.19 49.69
á-Linolenic acid(18:3) 4.7±0.44
Arachidic acid 1.26
Lignoceric acid
% TSFA 32.63
%TUFA 67.37
%MUFA 10.61
%PUFA 56.49
Phenolics such as pcoumaric acid or vanillic acid
were also detected in pigeon pea. The phytochemical analysis
of leaf seed and stem extracts of pigeon pea showed the
presence of saponins, tannins, alkaloids flavonoids,
anthraquinones and reducing sugars (Harris et al. 2014), but,
cardiac glycosides and terpenoids were absent in some of
the components of pigeon pea. Pigeon pea is a good source
of alkaloids (Aja et al. 2015). The results also revealed that
anthocyanins were found to be present in the leaf and seed
of pigeon pea and the leaves contain more of the bioactive
compounds than the seeds suggesting the use of different
parts of pigeon pea plant on various diseases (Ade-Omowaye
et al. 2015).
Health benefits: The nutritional components of pigeon pea
are widely considered crucial for human nutrition, because
of phytochemicals, bioactive compounds which play vital
roles in humans. Traditionally Cajanus cajan leaves have
been used by Rabha tribe to cure jaundice and also described
as useful for the treatment of smallpox, chicken pox, measles
and also as an astringent, mouthwash by local people of North
East India (Sarma et al. 2015).
Pigeon pea can be a source of remedy in the control
of sickle cell anaemia. In India, many Sickle cell disease
(SCD) patients are using pigeon pea for effective
management of erythrocytes sickling in Chhattisgarh (Verma
2015). In an ethnomedical survey pigeon pea plant was
216 ASIAN JOURNAL OF DAIRY AND FOOD RESEARCH
recorded as traditional medicinal plant used in Northern and
South-Eastern Côte d’Ivoire for the treatment of anaemia
(Kone 2011). Pigeon pea also has anti-ulcer potential
(Mansoor 2015).
The European Society of Hypertension reco mm
ends diet and lifestyle approaches as a basis for prevention
and treatment of hypertension. From animal model, it was
both water extracts of pigeon pea and water extracts of B.
subtilis fermented pigeon pea improved systolic blood
pressure and diastolic blood pressure in spontaneously
hypertensive rats (Lee et al. 2015).
Use as functional foods: A study was conducted to investi
gate the survival of Lactobacillus reuteri ATCC 55730 in
creams, prepared with pigeon peas and oat. The study
concluded that L. reuteri ATCC 55730 had the highest
viability in cream with 40% pigeon pea and 20% oat
(Barboza et al. 2012). The effect of the use of pigeon pea as
a substrate in the production of a legume-based fermented
product with Lactobacillus acidophilus ATCC 314 or
Lactobacillus casei ATCC 393 was studied by Parra et al.
Pigeon pea-based fermented probiotic product was suitable
for both the strains (Parra et al. 2013).
In a study, the effects of a dietary prebiotic, inulin
and probiotic was investigated in mice using cellulose-based
AIN-93G diets under conditions allowed for the growth of
commensal bacteria (Kuo et al. 2013).
Prebiotic potential: A prebiotic is defined as a selectively
fermented ingredient that allows specific changes, both in
the composition and/or activity in the gastrointestinal
microflora that confers benefits upon host well-being and
health (Roberfroid et al. 2010). Fermentation of dietary
carbohydrates provides the energy for the growth and activity
of the intestinal microbiota.
Several studies established the role of prebiotics in
weight control, by improving microbial balance, ameliorating
adiposity and increasing mucosal integrity with decreased
inflammation (John et al. 2012). A number of mechanisms
have been implicated in the link between intestinal
microbiota, increased fatty acid metabolism, and storage of
calories as fat (Mallappa et al. 2012). The prebiotics can be
a tool to modulate gut microbiota which plays a role in the
pathophysiology of obesity.
A diet rich in non-digestible carbohydrates induced
significant weight loss and concomitant structural changes
of the gut microbiota in simple obese children (Zhang et al.
2015). In another study consumption of prebiotics for 16
weeks significantly improved bifidobacterial abundance in
overweight and obese children and proved that prebiotic fiber
is a potential treatment option to reduce body fat by gut
microbiota modulation (Nicolucci et al. 2015).
Recently Devindra et al. (2017) have demonstrated
the prebiotic potential of red gram raffinose oligosaccharides
in an animal model. The results of the prebiotic potential of
red gram oligosaccharides have shown a hypolipidemic effect
and lowered blood glucose level, improved HDL and
decreased LDL. This new array of research may provide
enough evidence for the prebiotic potential of pigeon pea.
Antioxidant potential: The bioactive compounds of pigeon
pea seeds contain some defense machinery. Four important
compounds, pinostrobin, cajaninstilbene acid (CSA), vitexin
and orientin isolated from ethanolic extracts of pigeon pea found
to possess significant antioxidant activities (Pal et al. 2011).
Antioxidant potential of pigeon pea seed husk was
investigated and results revealed a potent anti-oxidant
activity (Rani et al. 2014). The aqueous extract of the pigeon
pea had the highest antioxidant activity possibly because of
the presence of polyphenols (Mahitha et al. 2015). Uchegbu
and Ishiwu (2015) studied antioxidant activity of extract of
germinated pigeon pea in alloxan-induced diabetic rats.
Consumption of germinated pigeon pea extract resulted in
reduction of fasting blood glucose level and LPO in diabetic
rats (Uchegbu and Ishiwu 2015).
Table 7: Anti-nutritional factors in pigeon pea (g/100g).
Constituents Nwaogu & Emejulu, Nwosu et al. Balogun, (2013) Harris, (2014) Aja, (2013)
(2010) (mg/100g) (2013) (g/100g) (mg/100g) (g/100g) (mg/100g)
Alkaloids 0.323 2.65±0.01 385.54±75.15
Phenol 0.160 3.82±0.15
Flavono 2.11±0.03 31.08±8.20
Saponin 5.10±0.20 0.466 1.19 6.35±0.96 1.82±0.29
Tannin 0.10±0.01 0.220 1.05 0.23±0.01 17.30±0.47
Hydrogen cyanide 7.180** 0.65
Phytate 11.57±1.20 1.017 1.81
Oxalate 28.58±1.02 0.139 0.14 —
Trypsin inhibitor 3.80±0.10* — —
Cyanogenic glycoside 12.42±1.84
Glycosides — — —- — 3.80±1.01
Anthocyanin —- 4.75± 0.17
*TIU/100g, ** mg/100g
Volume 37 Issue 3 (September 2018) 217
Hypocholesterolemic effect: The consumption of pulses and
legumes has been reported to ameliorate serum cholesterol
levels and increase the saturation levels of cholesterol in the
bile. Pigeon pea is a good source of saponins which have
been implicated for the control of high cholesterol level and
they bind to the bile salts (Aja et al. 2015).
Overweight and obesity: The diet high in whole grains is
associated with the lower body mass index, smaller waist
circumference, reduced risk of overweight and obesity (Butt
et al. 2011). Pigeon pea has high protein content and this
dietary protein may promote weight loss by inducing satiety
hence decrease energy expenditure. Using data from the
National Health and Nutrition Examination Survey (NHANES),
it was observed that adults who consumed a variety of
legumes had significantly lower body weights compared with
those who did not consume legumes (Polak 2015).
Role in diabetes (Hypoglycemia): It is acknowledged that
certain fibre rich foods like whole pulses can affect glycemic
control in diabetes and hyperlipidemia. Pigeon pea is the
most effective hypoglycemic medicinal plant commonly
studied in relation to diabetes and their complications and
owing to its varied degree of hypoglycemic activity. In a
study substitution of red meat with legumes improved lipid
profiles and glycemic control among diabetes patients
(Hosseinpour-Niazi 2015).
In another study, there was a reduction in glucose
levels of rats treated with ethanol extract of pigeon pea leaves
and an increase in ALT, AST and ALP levels when compared
with those treated with Moringaoleifera extract (Aja et al.
2015b). In a study, crude methanol extract of pigeon pea
seed husks mitigated starch-induced postprandial glycemic
excursions and reduced glycemic load in rats similar to the
standard drug acarbose (Tiwari et al. 2013). The hypogl
ycemic effect of crackers produced from sprouted pigeon
pea caused hypoglycemic effect in diabetic rats and led to a
reduction of measured biochemical indices (Uchegbu 2016).
Cancer prevention: Alkaloids of pigeon pea have been
implicated for inducing a stress response and apoptosis in
human breast cancer cell. DNA fragmentation was observed
in human breast cancer cells treated with cajanol, a novel
anticancer agent from pigeon pea roots (Luo et al. 2010).
The methanol extract of the plant has been shown to
demonstrate cytotoxicity against three cancer cell lines,
namely human breast adenocarcinoma cell line MCF-7,
human large cell lung carcinoma cell line COR-L23 and
human amelanotic melanoma C32 (Ashidi et al. 2010).
Anti-inflammatory: In another study, the ethanol extracts
of pigeon pea and cyanidin-3-monoglucoside suppressed the
production of inflammatory cytokines, including TNF-α, IL-
1β, and IL-6 (Lai et al., 2012). Hence, pigeon pea leaves
can be developed as an effective herbal remedy for the
treatment and prevention of inflammation or associated
ailments (Patel and Bhutani 2014).
In a recent study, the pigeon pea extract inhibited
carrageenan-induced inflammation by 85 and 95%, respec
tively. This was accompanied by a decrease of TNF-α and
IL-6, as well as significant decrease in IgG serum levels
(Hassan et al. 2015).
Antimicrobial effect: Pigeon pea plant extract is inhibitory
to some bacterial pathogens (Braga et al. 2007). The leaf
part of pigeon pea is an excellent source of natural
antimicrobial substances. Moreover, cajanuslactone is a
potential anti-bacterial agent against Gram-positive
microorganisms (Kong et al. 2010). The presence of tannins,
flavonoids and alkaloids in pigeon pea extract has clinically
relevant antifungal activity (Brito et al. 2012).
A study investigated the protective effect of
cajaninstilbene acid against corticosterone induced injury
in PC12 cells and examined the potential mechanisms for
the same (Jiang et al. 2014). Different extracts of leaf, seed
and root of the pigeon pea were proven to be a great potential
source of antibacterial compounds (Devi et al. 2016) and
also aid in wound healing activity. In a study, wound healing
activity of hydrogel obtained from pigeon pea seed husk was
carried out in albino rats. Gel formulation showed significant
antibacterial activity against both gram positive and gram
negative selected bacteria and the percentage wound closure
and epithelialization for the gel formulation treated group
was comparable with those of standard group treated with
Band aid (Patil and Mastiholimath 2011).
Hepatoprotective: Pigeon pea is already known for its
hepatoprotective function. Pigeon pea plant protein extracts
can up-regulate and counteract the inflammatory process,
minimize the damage to the liver, delay disease progression,
and reduce its complications in liver (Rizk et al. 2014) and
kidneys (Aly et al. 2016). The pigeon pea extract was
potential towards antioxidative protection against iron-
overload-induced liver damage in mice and improved hepatic
antioxidants (Sarkar et al. 2013).
Pigeon pea plant extract also had promising anthel
mintic effects against F. hepatica (Alvarez et al. 2015) and a
poly herbal formulation from pigeon pea could protect the liver
cells from CCl4 - induced liver damages (Arka et al. 2015).
In another study hepatoprotective activity of pigeon
pea was studied in sodium fluoride treated Swiss albino
(BALB/C) mice. Treatment with extract of pigeon pea
exhibited significant anti-oxidant and hepatoprotective
activity (Kayathri et al. 2015).
CONCLUSION
Pigeon pea is among the essential pulse in arid and
semiarid tropical areas of the world. It is a dense source of
nutrients and plays a promising role in human nutrition.
Pigeon pea in view of their nutrient profile seems to be ideal
for inclusion in designing snack foods, baby and sports foods.
Various parts of pigeon pea have already been utilized for
therapeutic use since ages.
218 ASIAN JOURNAL OF DAIRY AND FOOD RESEARCH
From this review, it was noted that pigeon pea is a
good source of antioxidants and can prevent the oxidative
stress related disorders like cancer and cardio vascular
diseases. Consumption of pigeon pea has several health
benefits due to the presence of bioactive compounds and
helps in the weight management, alleviating cholesterolemia
and diabetes hence can be a remedy to metabolic syndrome
as well.
The hepatoprotective potential of pigeon pea is
promising since it has a vital role in the control of liver
damage. The past decade has seen several new trends in the
field of application of pigeon pea in neutraceutical industry.
Pigeon pea can also be an alternative to artificial nutrition
formulas which induce a low grade inflammation. Hopefully,
research will soon offer enough data to show the efficacy of
pigeon pea in gut health by possible biochemical alterations.
Further research is in need to understand the role
of pigeon pea prebiotics to prevent or control diabetes,
obesity, cardiovascular diseases, irritable bowel syndrome
and other health benefits and understand the underlying
mechanisms that could greatly contribute to disease
prevention strategies in humans.
ACKNOWLEDGMENT
We thank Dr. R. Hemalatha, Director, National
Institute of Nutrition (ICMR) for her continuous support.
Conficts of interest
The authors declare that they have no conûicts of interest
REFERENCES
Adamu AS and Oyetunde JG (2013) Comparison of dietary proximate and mineral values of two varieties of bean. Asian J Natu Appl
Sci 2: 103-106.
Ade-Omowaye BIO, Tucker GA, and Smetanska I (2015) Nutritional potential of nine underexploited legumes in South west Nigeria.
Int Food Res J. 22:798-806.
Aja PM, Alum EU, Ezeani NN, Nwali BU, Edwin N (2015a) Comparative Phytochemical Composition of Cajanus cajan Leaf and
Seed. Int J Micr Res 6: 42-46.
Aja PM, Igwenyi IO, Ugwu Okechukwu PC, Orji OU, Alum EU (2015b) Evaluation of Anti-diabetic effect and liver function indices
of ethanol extracts of moringa oleifera and cajanus cajan leaves in alloxan induced diabetic albino rats. Global Veterinaria
14: 439-447.
Akande KE, Abubakar MM, Adegbola TA, Bogoro SE, Doma UD (2010) Chemical evaluation of the nutritive quality of pigeon pea
(Cajanus cajan (L). Millsp.). Int J Poultry Sci 9: 63-65.
Akporhonor EE, Egwaikhide PA, Eguavoen IO (2006) Effect of Sprouting on invitro digestibility of some locally consumed leguminous
seeds. J Appl Sci Env Man 10: 55-58.
Alvarez-Mercado JM, Ibarra-Velarde F, Alonso-Diaz MA, Vera-Montenegro Y, Avila-Acevedo JG,Gar cía-Bores AM (2 015) I n vitro
antihelmintic effect of fifteentropical plant extracts on excysted flukes of Fasciola hepatica. BMC Vete Res 11(45) 1- 6.
Aly HF, Rizk MZ, Abo-Elmatty DM, Desoky MM, Ibrahim NA, Younis EA (2016) Therapeutic and protective effects of Caesalpiniagilliesii
and Cajanus cajan proteins against acetaminophen overdose-induced renal damage. Toxicol Ind Health 32: 753-68.
Apata D (2008) Effect of cooking methods on available and unavailable carbohydrates of some tropical grain legumes. Afri J Biote
7: 2940–2945.
Arka G, Anindita K, Ankit S, Kumar SA, Kumar MS (2015) Preliminary evaluation of hepatoprotective potential of the polyherbal
formulation. J Intercult Ethno 4: 118-24.
Ashidi JS, Houghton PJ, Hylands PJ, Efferth T (2010) Ethnobotanical survey and cytotoxicity testing of plants of South-western
Nigeria used to treat cancer, with isolation of cytotoxic constituents from Cajanus cajan Millsp. leaves. J Ethnophar 128: 501-12.
Balogun BI (2013) Comparative evaluation of nutritive value of pigeon pea (Cajanus cajan (L.)Willsp.) and cowpea (VignaUnguiculala
(L.) Walp). J VocaTech Edu 10: 109-121.
Bamidele OP and Akanbi CT (2013) Influence of gamma irradiation on the nutritional and functional properties of pigeon pea (Cajanus
cajan) flour. Afr J Food Sci 7: 285-290.
Barboza Y, Márquez E, Parra K, Piñero MP, Medina LM. (2012) Development of a potential functional food prepared with pigeon pea
(Cajanus cajan), oats and Lactobacillus reuteri ATCC 55730. Int J Food Sci Nut 63: 813-20.
Braga FG, Bouzada MLM, Fabri RL, de O Matos M, Moreira FO, Scio E, Coimbra ES (2007) Antileishmanial and antifungal activity
of plants used in traditional medicine in Brazil. J Ethno Phar 111: 396–402.
Brito SA, Rodrigues FFG, Campos AR and da Costa JGM (2012) Evaluation of the antifungal activity and modulation between
Cajanus cajan (L.) Millsp. leaves and roots ethanolic extracts and conventional antifungals. Phar Magazine 8: 103-6.
Butt MS, Shahzadi N, Suleria H, Sultan T, Imran Chohan M (2011) Effect of dietary fiber in lowering serum glucose and body weight
in sprague dawley rats. Func Foods Health Disease 1: 261-278.
Cummings JH and Stephen AM (2007) Carbohydrate terminology and classification. Eur J Clin Nut 61: S5-18.
Devi RR, Premalatha R, Saranya A (2016) Comparative analysis of phytochemical constituents and antibacterial activity of leaf, seed
and root extract of Cajanus cajan (L.) Millsp. Int J Cur Mic Appl Sci 5: 485–494.
Devindra S and Aruna T (2016) Effect of Chemical Soaking, Toasting and Crude á-Galactosidase Enzyme Treatment on the Oligosaccharide
Content of Red Gram Flour. J Food Proc Pres doi: 10.1111/jfpp.12922.
Devindra S, Aruna T, Hemalatha R and Mohammed S (2017) Hypolipidemic effect of red gram (Cajanus cajan L.) prebiotic oligosaccharides
in Wistar NIN Rats. J Diet Suppl DOI: 10.1080/19390211.2017.1350246.
Volume 37 Issue 3 (September 2018) 219
Devindra S, Shilpa C, Charu K, Aruna T, Prasad GBKS (2016). Estimation of glycemic carbohydrate and glycemic index / load of commonly
consumed cereals, legumes and mixture of cereals and legumes. Int J Diab Deve Coun doi:10.1007/s13410-016-0526-1.
Devindra S, Sreenivas RJ, Bhaskar V, Mulimani VH (2012) Effect of heat treatment on á-galactoside content of red gram seeds
(Cajanus cajan, L). J Food Proc Pres 36: 97-103.
Ellong EN, Billard C, Adene S, Rochefort K (2015) Polyphenols, carotenoids, vitamin C content in tropical fruits and vegetables and
impact of processing methods. Food Nut Sci 6: 299-313.
Eltayeb ARSM, Ali AO, Haron R (2010) The chemical composition of pigeon pea (Cajanus cajan) seed and functional properties of
protein isolate. Pakistan J Nut 9: 1069-1073.
Faris DG and Singh U (1990) Pigeon pea: Nutrition and Products. In: Nene, Y.L., Hall, S. D. and Sheila, V.K. Eds., The Pigeonpea,
CAB International, Wallingford, 401-434.
Faris DG, Saxena KB, Marumadar S and Singh U (1987) Vegetable pigeon pea promising crop in India. ICRISAT, Patancheru, AP, India.
Harris KK, Sahu M, Verma D (2014) Phytochemical analysis of the leaf, stem and seed extracts of Cajanus cajan L (Dicotyledoneae,
fabaceae). World J Phar Sci 3: 694-733.
Hassan EM, Matloub AA, Aboutabl ME, Ibrahim NA, Mohamed SM (2015) Assessment of anti-inflammatory, anti-nociceptive,
mmunomodulatory, and antioxidant activities of Cajanus cajan L. seeds cultivated in Egypt and its phytochemical composition.
Phar Biol 9: 1-12.
Hosseinpour-Niazi S, Mirmiran P, Hedayati M and Azizi F (2015) Substitution of red meat with legumes in the therapeutic lifestyle
change diet based on dietary advice improves cardio metabolic risk factors in overweight type 2 diabetes patients, a cross-
over randomized clinical trial. Eur J Clin Nut 69: 592-7.
International year of pulses. http,//iyp2016.org/about-us
Jairo OC, Hugo CS, Gilberto LB and Roberto de, C (1991) Oligosaccharide levels in immature and mature seeds from several varieties
of pigeon peas (Cajanus cajan). Alimento s Nutricao araraquara. 3: 75-85.
Jiang BP, Liu YM, Le L, Li ZY, Si JY, Liu XM, Chang Q, Pan RL (2014) Cajaninstilbene acid prevents corticosterone-induced apoptosis
in PC12 cells by inhibiting the mitochondrial apoptotic pathway, Cell Phys Biochem 34: 1015-26.
John K, Di Baise, Daniel N, Frank and Ruchi Mathur (2012) Impact of the gut microbiota on the development of obesity: Current
Concepts. American Journal of Gast Supp 1: 22-27.
Kayathri D, Kalaimathi RV, Karthick Rajan D and Sivamani P (2015) Hepatoprotective activity of Cajanus cajan in sodium fluoride
treated swiss albino (balb/c) mice. World J Phar Sci 4:1805-1814.
Keshav KB (2015) Optimization of High Fiber Bun Formula and its Nutritional Evaluation. Int J Human Nut Diet 3: 89-93.
Kone W, Koffi A, Bomisso E, Tra Bi F (2011) Ethnomedical Study and Iron Content of Anaemia. African J Trad Comp Alte Med 9:
81–87.
Kong Yu, Yu-Jie Fu, Yuan-Gang Zu, Fang-Rong Chang,Yung-Husan Chen, Xiao-Lei Liu, Johannes Stelten, Hans-Martin Schiebel
(2010) Cajanuslactone, a new coumarin with anti-bacterial activity from pigeon pea (Cajanus cajan (L.) Millsp.) leaves.
Food Chem 121: 1150-1155.
Kunyanga C, Imungi J and Vellingiri V (2013) Nutritional evaluation of indigenous foods with potential food-based solution to
alleviate hunger and malnutrition in Kenya. J App Biosci 67: 5277-5288.
Kuo SM, Merhige PM and Hagey LR (2013) The effect of dietary prebiotics and probiotics on body weight, large intestine indices, and
fecal bile acid profile in wild type and IL10-/- mice. PloS One, 8: e60270.
Lai YS, Hsu WH, Huang JJ and Wu SC (2012) Antioxidant and anti-inflammatory effects of pigeon pea (Cajanus cajan L.) extracts on
hydrogen peroxide- and lipopolysaccharide-treated RAW264.7 macrophages. Food Function 3: 1294–301.
Lee BH, Lai YS, Wu SC (2015) Antioxidation, angiotensin converting enzyme inhibition activity, nattokinase, and anti-hypertension
of Bacillus subtilis (natto)-fermented pigeon pea. J Food Drug Analysis 23: 750–757.
Longvah T, Ananthan R, Bhaskara Chary K and Venkaiah K (2017) Indian food composition tables. ICMR, New Delhi, India.
Luo M, Liu X, Zu Y, Fu Y, Zhang S, Yao L, Efferth T (2010) Cajanol, a novel anticancer agent from Pigeon pea (Cajanus cajan (L.)
Millsp.) roots, induces apoptosis in human breast cancer cells through a ROS-mediated mitochondrial pathway. Chemi Biol
Inter 188: 151–60.
Mahitha B, Archana P, Ebrahimzadeh MDH, Srikanth K, Rajinikanth M, Ramaswamy N (2015) In vitro antioxidant and pharmacognostic
studies of leaf extracts of Cajanus cajan (l.) millsp. Indian J Pharm Sci 77: 170-177.
Mallappa RH, Rokana N, Duary RK, Panwar H, Batish VK, Grover S (2012) Management of metabolic syndrome through probiotic
and prebiotic interventions. Indian J End Met 16: 20-7.
Mansoor M, Venkateswarlu C, Rao S (2015) Phytochemical and antiulcer activity of Cajanus cajan leaves against Pylorus ligation-
induced gastric ulcer in rats. International J Adv Phar Med Bio Sci 3: 84-88.
Mulimani V and Devindra S (1998) Effect of soaking, cooking and crude α-galactosidase treatment on the oligosaccharide content of
red gram flour. Food Chem 61: 475-479.
Nicolucci A, Hume M, Reimer R (2015) Effect of Prebiotic Fiber-Induced Changes in Gut Microbiota on Adiposity in Obese and
Overweight Children. FASEBJ 29: 276-6.
Nwaogu L, Emejulu A (2010) Evaluation of the toxicity of cyanogens in a commonly consumed Nigeria legume pigeon pea (Cajanus
cajan) seed and its biochemical effects in rabbits. Int J Bio Chem Sci 4: 1435-1441.
Nwokolo E (1987) Nutritional evaluation of pigeon pea meal. Plant Food for Hum Nutr 37: 283- 290.
220 ASIAN JOURNAL OF DAIRY AND FOOD RESEARCH
Nwosu JN, Ojukwu M, Ogueke CC, Ahaotu I and Owuamanam CI (2013) The Anti-nutritional properties and ease of Dehulling on the
proximate composition of Pigeon Pea (Cajanu scajan) as affected by malting. Int J Life Sci 2: 60-67.
Oke DG (2014) Proximate and phytochemical analysis of cajanus cajan (Pigeon Pea) leaves. Chem Sci Tran 3:1172-1178.
Olalekan AJ, Bosede BF (2010) Comparative study on chemical composition and functionalproperties of three Nigerian legumes (Jack
beans, Pigeon pea and Cowpea). J Emer Trends Eng App Sci1: 89–95.
Pal D, Mishra P, Sachan N, Ghosh AK (2011) Biological activities and medicinal properties of Cajanus cajan (L) Millsp. J Adv Phar
Tech Res 2: 207-14.
Panlasigui L. N, Panlilio LM, Madrid JC (2009) Glycemic response in normal subjects to five different legumes commonly used in the
Philippines. Int J Food Sci Nut 46:155-160.
Parra K, Ferrer M, Piñero M, Barboza Y, Medina LM (2013) Use of Lactobacillus acidophilus and Lactobacillus casei for a potential
probiotic legume-based fermented product using pigeon pea (Cajanus cajan). J Food Prot 76: 265-71.
Patel NK and Bhutani KK (2014) Pinostrobin and Cajanus lactone isolated from Cajanus cajan (L.) leaves inhibits TNF-αand IL-1β
production, in vitro and in vivo experimentation. Phytomedicine 21: 946–53.
Patil BS and Mastiholimath VS (2011) Wound healing activity of hydrogel obtained from pigeonpea (Cajanus cajan) seed husk. J
Chem Phar Sci 4: 108-110.
Pigeon pea in Eastern and Southern Africa http://exploreit.icrisat.org/page/eastern and southern Africa /887/329. ICRISAT
Polak R, Phillips EM and Campbell A (2015) Legumes, health benefits and culinary approaches to increase intake. Clin Diab 33: 198–205.
Rani S, Poswal G, Yadav R and Deen MK (2014) Screening of pigeon pea (Cajanus cajan L.) seeds for study of their flavonoids, total
phenolic content and antioxidant properties. Int J Pharm Sci Review Research 28: 90-94.
Rizk MZ, Aly HF, Abo-Elmatty DM, Desoky MM, Ibrahim N, Younis EA (2014) Hepatoprotective effect of Caesalpiniagilliesii and
Cajanus cajan proteins against acetoaminophen overdose-induced hepatic damage. Tox Ind Health 32: 877-907.
Roberfroid M, Gibson GR, Hoyles L, McCartney AL, Rastall R, Rowland I, Wolvers D, et al., (2010) Prebiotic effects, metabolic and
health benefits. Bri J Nutr 104: S1-S63.
Sangle SM (2015) Studies of mineral constituents in viable mutants of pigeon pea seeds. Bio sci Disc 6: 112-116.
Sarkar R, Hazra B and Mandal N (2013) Anti-oxidative protection against iron overload-induced liver damage in mice by Cajanus
cajan (L.) Millsp.leaf extract. Indian J Exp Biol 51:165-73.
Sarma A, Dutta T, Sarma P (2015) Screening of phyto-chemicals with respect to antioxidant properties of certain ethno-medicinally
important plants from NE India. Ann Phar Res 3:132-135.
Singh J, Basu P (2012) Non-nutritive bioactive compounds in pulses and their impact on human health: An Overview. Food Nutr Sci
3:1664-1672.
Singh U, Praharaj CS, Singh SS and Singh NP (2016) Bio fortification of Food Crops. New Delhi, Springer India.
Tiwari A, Abhinay B, Babu K, Amtul Zahera A (2013) Pigeon pea seed husks as potent natural resource of anti-oxidant and anti-
hyperglycaemic activity. Int J Green Phar 7: 252-257.
Uchegbu NN (2016) Consumer acceptability of crackers produced from blend of sprouted pigeon Pea, unripe plantain and brewers
spent grain and its hypoglycemic effect in diabetic Rats. World Academy of Science, Engineering and Technology, Int J Nut
Food Sci 3: 374-378.
Uchegbu NN and Ishiwu CN (2015) Nutritional composition of crackers produced from blend of sprouted pigeon pea (Cajanus cajan),
unripe plantain (musa parasidiaca) and brewers’ spent grain flour and blood glucose level of diabetic rats fed the biscuit.
World Acad Sci Eng Tech 10: 1-5.
Van der, Maeson, L.J.G.(1995) Pigeon pea Cajanus cajan, in, Evolution of Crop Plants. [Smartt, J. and Simmonds, N. W. (eds.)]
Essex, Longman pp. 251–5.
Verma H (2015) Phytochemical characterization of twelve medicinal plants used for sickle cell disease management in Chhattisgarh.
Int J Phar Bio Sci 6: 1062–1070.
Zhang C, Yin A, Li H, Wang R, Wu G, Shen J, Zhang M, Wang L, Hou Y, Ouyang H, et al (2015) Dietary modulation of gut microbiota
contributes to alleviation of both genetic and simple obesity in children. E Bio Medicine 2: 968–984.
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The effects of soaking in 1 and 2% sodium bicarbonate solution, toasting, roasting followed by boiling and crude α-galactosidase treatment on the levels of the raffinose family of sugars in red gram (Cajanus cajan, L) seeds were investigated. The percent removal of raffinose (43.05 and 73.80%), stachyose (15.80 and 70.27%) and verbascose (18.07 and 51.71%) after soaking in 1 and 2% of sodium bicarbonate solution of red gram seeds for 16 h, respectively. Roasting of red gram seeds for 20 min led to a mean reduction of 64.17% for raffinose, 61.67% for stachyose and 57.53% for verbascose and toasting followed by boiling led to a mean reduction of 19.80% for raffinose, 33.20 for stachyose and 45.58% for verbascose, respectively. The treatment of red gram flour with partially purified α-galactosidase from Aspergillus niger for 3 h was effective in reducing the levels of the raffinose family of sugars. The processing methods such as soaking in sodium bicarbonate solution (1 and 2%) toasting, roasting followed by boiling and crude α-galactosidase from Aspergillus niger treatment are employed to reduce the flatulence inducing raffinose family sugars in legume. Effect of soaking in 2% sodium bicarbonate solution for 16 h led to highest reduction of raffinose family sugars than that of soaking in 1% sodium bicarbonate solution. Toasting of red gram seeds for 20 min has been found to moderate reduction of raffinose family sugars. Roasting for 5 min followed by 20 min boiling found to be low levels of reduction of raffinose family sugars. Whereas the partially purified α-galactosidase from A. niger was effective in reducing the levels of the raffinose family of sugars in all the cultivars studied. Enzymatic treatment for 3 h completely removed the flatus-inducing factors, as evidenced by TLC analysis. This information could further stimulate application of these inexpensive and easy methods for the removal of raffinose family of sugars in different varieties of legume seeds.
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The tumor necrosis factor alpha (TNF-alpha) and interleukin 1 beta (IL-1 beta) inhibitory activities of Cajanus cajan (leaves) crude methanolic extract, its fractions and its phytochemical constituents were evaluated in lipopolysaccharide (LPS) stimulated RAW 264.7 and J774A.1 cells. Phytochemical investigation of the active ethyl acetate (CCE) and n-butanol (CCB) fractions of C cajan L leaves yielded 14 compounds. It was observed that both pinostrobin (9) and cajanus lactone (4) were found to be most active in inhibiting TNF-alpha (IC50 <22 mu M) and IL-1 beta (IC50 < 40 mu M) whereas compounds 2, 3, 5-8, 10 and 14 showed moderate and mild effects (IC50 = 35.50-81.22 mu M for INF-alpha and 38.23-89.10 mu M for IL-1 beta) in both the cell lines. Furthermore, at dose of 20 mg/kg, both pinostrobin (9) and cajanus lactone (4) were found to reduce LPS-induced TNF-alpha levels by 48.6% and 55.0% respectively and IL-1 beta levels by 53.1% and 41.8% respectively in Sprague Dawley (SD) rats. These findings suggest that C cajan L leaves can be developed as an effective herbal remedy for the treatment and prevention of inflammation or associated ailments.
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The hypolipidemic effect of red gram prebiotics of raffinose family oligosaccharides was studied in Wistar National Institute of Nutrition male rat strain. The study consisted of 36 rats randomly divided into three groups of 12 rats each. For 16 weeks, Group I was fed with the control diet; Group II was fed with a diet containing 3% standard raffinose as the reference group; Group III received the diet containing 3% red gram prebiotics. The results showed that the gain in body weight was low in the red gram prebiotics–supplemented group followed by the control group; highest increase of body weight was seen in the raffinose standard–fed group. Serum glucose levels of the red gram prebiotic–fed group decreased 14.92% compared to the control group and increased 2.07% compared to the reference group. The decrease in serum triglycerides (TG) levels of the red gram prebiotic-fed groups was 32.76% compared to the control group and 33.64% compared to the reference group. Decrease in the serum TC of the red gram-fed animals was 18.51% and 4.63% compared to the control group and the reference group, respectively. Increase in the level of serum high-density lipoprotein cholesterol (HDL-C) in the red gram-fed animals was 18.51% compared to the control group and 4.63% compared to the reference group. The present study can be a proof for the use of prebiotics as a preventive measure for overweight and obesity in humans, and legume prebiotics can be explored as a novel prebiotic product in the consumer market.
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ORIGINAL RESEARCH ARTICLE ABSTRACT ARTICLE INFORMATION Background: The present study was designed to investigate the antiulcer potential of ethanolic leaves extract of Cajanus cajan. Material and methods: Antiulcer activity was evaluated by pylorus ligation induced ulcer models in rats. The ethanolic extract of the leaves of Cajanus cajan was given by oral route at a dose of 250 and 500mg/kg b.w. Results: Ethanolic extract of Cajanus cajan, dose dependently reduce, the total acidity, ulcer index, and an increase in pH of gastric juice in pylorus ligated ulcer model. Conclusion: Extract of Cajanus cajan may be useful as a natural antioxidant in the treatment of ulcer.