ArticlePDF Available

Medicinal Properties of Desert Date Plants (Balanites aegyptiaca)-An Overview

Authors:

Figures

Mesocarp Fig. 5: Endocarp Fig. 6: Kernel Botanical History: Balanites aegyptica (L.) Delile (the Taxonomic Classification: The taxonomic classification of desert date or Heglig tree) was first named as Agihalid B. aegyptiaca ( L. ) Del was reported by National Plant after the Arabic name'Heglig'in 1592 by Prosper Alpinio Data Center [42], as seen below: [37]. In 1753 Linnaeus described it as Ximenia aegyptiaca, while in 1813 Delile replaced Agihalid name by Balanites which was originally a Greek word acorn, meaning the fruit [37,38]. The placement of the genus Balanites was debatable a long its history. It was originally placed in Zygophyllaceae then shifted to Olacaceae, Simaroubaceae and finally Balanitaceae. Boesewinkel [39], supported the recognition of a separate family Balanitaceae based on its unique ovule and seed characters. The molecular work on floral anatomy, embryology, taxonomy and pollen morphology supported the retention of the genus under Zygophyllaceae [40, 41]. However, according to very thorough and extensive review it was recognized as independent separate family of Balanitaecae [2, 37]. This revision concluded that the whole genus Balanites has nine species and eleven intraspecific taxa (1-Balanites wilsoniana (var. wilsoniana, var. mayumbensisandf var. glabripetata); 2-Balanites maughamii (subsp. Maughamii and subsp. Acuta); 3-Balanitestriflora; 4-Balanitesroxburghii; 5-Balanitesaegyptiaca (var. aegyptiaca, var. ferox, var. pallida, var. quarrrei and var. tomentosa); 6-Balanitespedicellaris (subsp.. pedicellaris and subsp. Somalensis); 7-Balanitesangolensis, (subsp. Angolensis and subsp. Welwitschii); 8-Balanitesrotundifolia, (var. rotundifolia, var. scillia and var. setulifera); 9Balanitesglabra)
… 
Content may be subject to copyright.
Global Journal of Pharmacology 12 (1): 01-12, 2018
ISSN 1992-0075
© IDOSI Publications, 2018
DOI: 10.5829/idosi.gjp.2018.01.12
Corresponding Auhor: Saed A. Al-Thobaiti, Department of Biological Sciences, Faculty of Sciences,
King Abdulaziz University, P.O. Box 139109, Jeddah 21323, Saudi Arabia.
Tel: +966503052017, E-mail: saiad1402@gmail.com.
1
Medicinal Properties of Desert Date Plants
(Balanites aegyptiaca) – An Overview
Saed A. Al-Thobaiti and Isam M. Abu Zeid
Department of Biological Sciences, Faculty of Sciences,
King Abdulaziz University, P.O. Box 139109, Jeddah 21323, Saudi Arabia
Abstract: Balanites aegyptiaca (L.) Del, an evergreen, woody, spinous flowering tree about 10 m height
referred to as ‘desert date,’ is a fabulous therapeutic source of curing ailments. It is a member of the family
Balanitaceea which is broadly spread in waterless land areas of Africa and Southern part of Asia. It consists
of saponins, flavonoids, alkaloids, lipids, proteins, carbohydrates and organic acids. Different parts of the
plant are confirmed to be utilized in folkloric medicines for the treatment of many diseases. These traditional
uses of B. aegyptiaca (L.) Del were scientifically proven by many studies including in vivo,in vitro and even
one pilot randomized controlled trial (RCT). This paper presents the folkloric and scientific review of the
B. aegyptiaca (L.).
Key words: Balanites aegyptiaca Folkloric Medicine Bioactive Compounds Pharmacological Properties
INTRODUCTION desert date (common name) and lalobe (Arabic name), is
Balanites aegyptiaca (L.) Del. is in the family of glabrous (Figure 2), after ripening [4]. It contains four
Balanitaceea.The word Balanites is derived from the layers [20]. The outer skin called epicarp (Figure 3), the
Greek word acorn, which means fruit by Alire Delile in fleshy pulp called mesocarp (Figure 4), the woody shell
1813, who substitute Agihalid name rooted from the called endocarp (Figure 5) and the inner seed called kernel
Arabic word heglig [1]. The entire genus of Balanites is (Figure 6). All of the four layers can be utilized for
consist of nine species and eleven intra-specific taxa [2]. different industrial and pharmaceutical products [21]. The
It is a true arid and semi arid multibranched, evergreen seed contains high amounts of oil [22-24]. The oil is
spiny tree species (Figure 1) with a wide range of consumed in human food [25, 26], or can be converted
geographical distribution [3]. It is found in the Sudan- into biodiesel [27, 28]. Also, the oil can used for medicinal
Sahel region of Africa, the Arabian Peninsula and South purposes [22]. The cake remains after oil extraction is a
Asia [4-6]. In addition to this wide distribution, it can also good source for animal feed supplement [29]. However,
grow in many soil type, including sand, heavy clay with the most important product obtains from different parts of
different climatic moisture levels [7, 8]. Also, the tree has the tree is the saponins. This compound proved to have
a good adaptive mechanisms to grow and thrive under wide range of industrial and pharmaceutical applications
combined water and salinity stresses [9]. [30, 31]. In other words, different parts of the plant were
Balanites is known to be multiple uses and multiple reported to have medicinal properties in many
users arid land tree with a wide range of products and ethnobotanical studies as antihelmenthic, a purgative,
values such as food, fodder, shade, oil and traditional leukoderma and emetic [27, 32]. It was also used as
medicine [10-13] and potential shelterbelts and anticancer, antivirus as well as antimicrobial [33, 34],
agroforestry species [14, 15]. However, the most important and act as a good antidiabetic and antioxidant agents
part of the tree is its fruits [16-19]. The fruit is known as [35, 36].
a drupe, pubescent when green, becoming yellowish and
Global J. Pharmacol., 12 (1): 01-12, 2018
2
Fig. 1: B.aegyptiaca Fig. 2: Fruit Fig. 3: Epicarp
Fig. 4: Mesocarp Fig. 5: Endocarp Fig. 6: Kernel
Botanical History: Balanites aegyptica (L.) Delile (the Taxonomic Classification: The taxonomic classification of
desert date or Heglig tree) was first named as Agihalid B.aegyptiaca ( L. ) Del was reported by National Plant
after the Arabic name‘Heglig’in 1592 by Prosper Alpinio Data Center [42], as seen below:
[37]. In 1753 Linnaeus described it as Ximenia
aegyptiaca, while in 1813 Delile replaced Agihalid name
by Balanites which was originally a Greek word acorn,
meaning the fruit [37,38]. The placement of the genus
Balanites was debatable a long its history. It was
originally placed in Zygophyllaceae then shifted to
Olacaceae,Simaroubaceae and finally Balanitaceae.
Boesewinkel [39], supported the recognition of a separate
family Balanitaceae based on its unique ovule and seed
characters. The molecular work on floral anatomy,
embryology, taxonomy and pollen morphology supported
the retention of the genus under Zygophyllaceae [40, 41].
However, according to very thorough and extensive
review it was recognized as independent separate family
of Balanitaecae [2, 37]. This revision concluded that the
whole genus Balanites has nine species and eleven
intraspecific taxa (1-Balanites wilsoniana (var.
wilsoniana, var. mayumbensisandf var. glabripetata);
2-Balanites maughamii (subsp. Maughamii and subsp.
Acuta); 3- Balanitestriflora; 4- Balanitesroxburghii;
5- Balanitesaegyptiaca (var. aegyptiaca, var.
ferox, var. pallida, var. quarrrei and var. tomentosa);
6- Balanitespedicellaris (subsp.. pedicellaris and subsp.
Somalensis);7- Balanitesangolensis, (subsp. Angolensis
and subsp. Welwitschii);8-Balanitesrotundifolia,(var.
rotundifolia,var. scillia and var. setulifera);9-
Balanitesglabra)
Taxonomic classification:
Kingdom Plantae – Plants
Subkingdom Tracheobionta – Vascular plants
Superdivision Spermatophyta – Seed plants
Division Magnoliophyta – Flowering plants
Class Magnoliopsida – Dicotyledons
Subclass Rosidae
Order Sapindales
Family Balanitaceea – Creosote-bush family
Genus Balanites Delile – balanites
Species Balanites aegyptiacus (L.) Delile – desert date
Synonyms: Ximenia aegyptiaca L. (excl. Balanites roxburghii Planch),
Agialida senegalensis van Tiegh., Agialida barteri van Tiegh., Agialida
tombuctensis van Tiegh., Balanites ziziphoides Milbr. Et Schlechter,
Balanites latifolia (van Tiegh.) Chiov [32].
Vernacular Names: Arabic (zachun, zaccone, heglig
(tree)), Lozi (mwalabwe); Luganda (musongole); Amharic
(kudkuda, jemo, bedeno), Jericho balsam,lalob tree, heglig,
Egyptian myrobalan, desert date, torch wood); French
(dattier sauvage, dattier du desert, myrobalau d' Egypte);
Hindi (engua, ingudi, betu, hingan, hingn, hingot, hongot,
hingota); Bemba (katikayengele, mubambwangoma)
Bengali (hin); English (soap berry tree, simple-thorned
torchwood, simple thorned torch tree, heglig berries (in
the sudan), Mandinka (sumpo); Nyanja (nkuyu); Sanskrit
(ingudi); Swahili (mjunju, mwambangoma); Tamil
(nanjunda); Tigrigna (indrur, mekie); Tongan
Global J. Pharmacol., 12 (1): 01-12, 2018
3
(mulyanzovu, mwalabwe); zacon, kuge, lalob (fruit)); Distribution and Habitat
Trade name (desert date (dried fruit, egyptian myrobalan) Ecology: Balanites aegyptiaca ( L. ) Del has extensive
[1]. ecological distribution; nevertheless, it reaches its
Botanical Features: Balanites aegyptiaca (L. ) Del is a with profound sandy loam and continuous access to
tree with multiple branches, spiny shrub having height of water like valley floors, river banks or the foot of rocky
10m. Crown rounded, dense (but still seen through) with slopes. It is intolerant to shade after the seedling stage
lengthy stout branchlets. Bark grey and trunk, intensely and therefore prefers open wood land or savannah for
fissured longitudinally [1, 7]. natural revival [43-45].
Leaves and Seeds: The plant has compound leaves with with a enormous geographical distribution. In Africa, its
spiral arrangement on its shoots, murky green with two region extends west to east, in the Sahelian band from the
firm coriaceous leaflets; having different shapes and Atlantic Ocean (Senegal, Mauritania) as far as Eritrea.
dimensions. Petiolecanaliculate, five mm to twenty mm This distribution extends across the Sahara, to Algeria
with a short rachis. It usually specifies a greatest length where its periphery is situated at 27 N; then in East
of eight mm for the plant in Uganda. Margin of every Africa in the strip going from Egypt and Libya, as far as
leafletentire; lamina commonly up to six cm long, four cm Zimbabwe (19 S), while in the Middle East from South to
broad, although actually lesser (1-3 x 0.3-1.5 cm) as in the North as far as latitude 35 25’ N, in the Arabian
Sahara and Palestine. The seed is pyrene, one and half to Peninsula, Burma, India and Pakistan, along the Arabian
three cm long, radiance brown, tough and extremely rigid. Gulf [43-45].
It makes up fifty to sixty percent of the fruit. About five
hundread to one thousand five hundread dry clean seeds Biophysical Limits: Orwa et al. [1] reported the following
per kg [7]. biophysical limits of B. aegyptiaca (L. ) Del:
Flowers and Fruits: Inflorescence is a dumpy Altitude: 0-2000 m, mean yearly temperature: twenty to
pedunculate fascicle of a few flowers. The flower buds are thirty degree, mean yearly rainfall: 250-1200 mm.
ovoid and covered with a short tomentose pubescence. A
flowers hermaphroditic, pentamerous an actinomorphic, is Type of Soil: It ranges from coarse sands, grimy clay
8-14 mm in diameter and generally greenish-yellow. loams, sandy loams or clays.
Pedicels heavily greyish, pubescent and rarely reaching10
mm in length, although 15 mm is reported for Zambia and Documented Species Distribution
Zimbabwe.The normal length is about 8 mm. Fruit Native: Djibouti, Egypt, Gambia, Kenya, Libyan Arab
ellipsoid, up to 4 cm long, green. Ripe fruit brown or pale Jamahiriya, Morocco, Myanmar, Chad, Cote d'Ivoire,
brown with a delicate coat enclosing a brown or brown- Democratic Republic of Congo, Benin, Burkina Faso,
green muggy pulp and a hardstone seed [7]. Nigeria, Burundi, Cameroon Sudan Saudi Arabia, Senegal,
Flowering and Fruiting Habit: The flowering behavior India, Israel, Tanzania, Uganda, Yemen, Republic of
differs, indeed, there is no specific time for its flowering in Zambia, Zimbabwe [1].
the Sahel region, where as it normally happens in the dry
season. Consequently, flowering season in Nigeria ranges Exotic: Cape Verde, Dominican Republic, Puerto Rico[1].
from November to April and fruits are ripen during
December and January and seldom from March to July. Ethnomedicinal and Folklore Reports: Although, there is
somewhere else, foliage and fruit production occur at the massive advancement in the field of synthetic drugs,
peak period of the dry season [7]. plants still hold their special importance, considering the
Pollination apparently takes place when the insects fact that they have no side effects. Different components
scents its flowers. It starts fruiting from 5-7 years, with an of B. aegyptiaca (L.) Del possess an enormous
rising yields for about two decades.These fruits actually convetional medicinal properties. On the other hand the
take at least a year to get matured and consequently ripen. therapeutic properties of the plant such as antihelminthic,
Mammals and birds eat the fleshy and safe fruit, throwing febrifuge, vermifuge, emetic, a purgative have been
away, reiterating, i.e discarding the seeds [7]. reported,it cures different types of diseases that include
maximum growth as an entity, low-lying, level alluvial sites
Also, B. aegyptiaca (L. ) Del is an Afro Asiatic tree
Eritrea, Ethiopia, Somalia, Algeria, Angola, Ghana, Guinea,
Global J. Pharmacol., 12 (1): 01-12, 2018
4
malaria, colds, skin boils, leukoderma, syphilis, liver and glucopyranosyl)-3- -[4-O-( -d-glucopyranosyl)-2-O-( -l-
spleen disorder, wound healing and pains [46]. The bark r hamnopyr a n o syl)- -d-glucopyranosyloxy]-22,26
of the plant is helpful in curing epilepsy, yellow fever, dihydroxyfurost-5-ene [57]. Nine saponins were
jaundice, mental diseases and syphilis and can at the isolated from kernel cake of B. aegyptiaca and out of
same time act as a fumigant for healing circumcision them, six were with molecular masses of 1196, 1064, 1210,
injuries [46]. The poach root of the plant are employed as 1224, 1078 and 1046Da were identifed, with the compound
a potage against stomach pain, anthrax and its concoction of mass 1210 Da being the main saponin present (ca. 36%)
serves as an antidote to snake bite [34]. The mixture of [23].
root bark has been documented to exterminate diarrhea, in
hemorrhoid, as well as a fish poison [33]. The paste of Flower: According to Umar et.al [58], the nutrient and
shoot is utilized for dressing of wounds and as tooth antinutritional content of B. aegyptiaca (L. ) Del flower
fluoresher. The thorns are employed as medicaments for composition found were ; ash (6.67±0.29%), moisture
healing leprosy. The leaf is employed in curing anthrax, (43.3±2.89%); crude protein (10.8±0.49%) crude lipid
due to their antihelminthic properties and as well as (4.5±0.50%), crude fibre (3.8±0.29%), available
flushing away malignant wounds [46]. The fruit cures oral carbohydrate (74.2±0.49%) and calorific value
ulcer, whooping cough, sleeping sickness and skin (380.5kcal/100g), Na (42.1mg/100g), K (81.8mg/100g), P
infections. Fruit kernel has been found as a mild laxative, (5.91mg/100g),Ca (49.8mg/100g), Mg (19.36mg/100g), Mn
an antidote for avoiding poisons and as a vermifuge [34]. (0.35mg/100g), Fe (31.46mg/100g), Cu (0.42mg/100g), Zn
The seeds are helpful in making cream for curing cough, (3.69mg/100g), Cd (0.19mg/100g), Co (0.33mg/100g), Cr
colic pain and at same time exhibit magicoreligious (0.35mg/100g) and Ni (6.33mg/100g).
properties [33, 34]. Due to its high percentage of carbohydrates content
Phytochemical Constituents an excellent source of energy and consequently contains
Leaves: The Egyptian species of the plant contains six adequate essential nutrients which include protein, lipid,
flavonoids which are quercetin 3-rutinoside, 3-glucosides, mineral elements and amino acids.
3-rutinoside, quercetin3-glucosides, 3-7 diglucoside and
3-rhamnogalactosides of isorhamnetin, which were Root: The specimen of the the East African roots
isolated from the leaves and branches [47]. Also, the revealed a Balanitin 1, 2 and 3, alkaloids and diosgenin
leaves, contain six diosgenin glucosides including di-, tri- [59-61]. Furthermore, it contains steroidal saponin1%
and tetraglucosides. Hydrolysis of the saponins gave glycosides with the major sapogenin is yamogenin
25D-spirosta-3, 5-diene and 3 -chloro-25D-spirost-5- [62, 63]. Other forms of glycosides are; (3 ,12 , 14 , 16 )-
ene[56-59] balanitin-1, -2 and -3[48-50]. 12 - h y d rox y c h ol est - 5 - en e- 3 , 1 6- di y l bi s ( -
Fruit: Mesocarp contains about 7.2% saponin, while 6.7% 25S)-26-( -D-glucopyranosyloxy)-22-methoxyfurost-5-en-
is found in the Kernel [51]. Balanitin A, B, C, D, E have 3-yl -D-xylopyranosyl-(1>3)- -D-glucopyranosyl-(1>4)[ -
been isolated from pulp while kernel contains only L r h a m n o p y r a n o s y l - ( 1 > 2 ) ] - -D-
Balanitin F and G [52].. The oil extracted from the kernel glucopyranoside;(3 ,20S,22R,25R) and (3 ,20S,22R,25S)-
composed mainly of triglycerides constituting 44–51% spirost-5-en-3-yl -D-xylopyranosyl-(1>3)- -D-
w/w, with little amount of diglycerides, phytosterols, glucopyranosyl-(1>4)[ -L-rhamnopyranosyl-(1>2)]- -D-
sterol esters and tocopherols [53]. Additionally, a famous glucopyranoside [64]. Balanitins 1 to 7 have also been
spirostanol glycoside, balanitin-3 and sapogenol, 6- reported from both root and bark of B.aegyptiaca (L.) Del
methyldiosgenin, furostanol saponin, balanitoside and [61, 65].
two pregnaneglycosides have been separated from the
fruits (mesocarp) of B. aegyptiaca (L. ) Del [54-56]. Stem Bark: The stem bark of the Indian species,
Chemical analysis proposed the chemical structure of the Balanites.Roxburghii contains balanitol and the
glycoside as 26-O- -dglucopyranosy l-3- saponins, deltoninand protodeltonin [66].
,22,26trihydroxy-furost-ene, 3-O- -lrhamnopyranosyl- Furanocoumarin, bergapten and a dihydrofuranocoumarin
(1>2)- -d-glucopyranosyl-(1>4)- dglucopyranoside and (marmesin) have been isolated from the chloroform extract
the saponins present in the mesocarp of B. aegyptiaca of the stem bark [67]. Balanitin 1, 2 and 3 have been
fruit are a mixture of 22R and 22S epimers of 26-(O- -d- isolated from East African species of B. aegyptiaca while
and calorific value as seen above, it is actually serves as
Dglucopyranoside), (3 , 20S, 22R, 25R)-, (3 , 20S, 22R,
Global J. Pharmacol., 12 (1): 01-12, 2018
5
diosgenin and sugars (glucose and rhamnose in the A prominent hyopoglycemic activity was reported
ratio 3:1) have been isolated from the Indian species from the water extract of mesocarps in the fruits of B.
Balanites roxburghii [66]. Dicholoromethane extract aegyptiaca (L.) Del on oral administration in
has yielded two different kind geometric isomers of streptozotocin-induced diabetic mice. It is believed that
alkaloid N-trans-feruloyltyramine and N-cis- the antidiabetic activity was due to the presence of
feruloyltyramine respectively and other metaboliteslike steroidal saponins in the extracts [77]. Additionally,
vanillic acid, syringic acid and 3 hydroxy-1-(4-hydroxy-3 homogeneous extracts of fruits using cell-based
methoxyphenyl)-1-propanone [69]. bioassays showed augmented basal glucose uptake by
Seeds: Four new cytostatic saponins have been extracted sugar particles [78]. Whereas, the dichloromethane and
from the seeds of B. aegyptiaca (L.) Del, namely, ethyl acetate extracts showed 37 and 41% increase in the
balanitins 4, 5, 6 and 7 [65]. Also, they contain deltonin glucose uptake, respectively [78]. Another possible
and isodeltonin which both are used as molluscicidal explanation of the hypoglycemic effect may be due to
agents [70]. trigonelline which was isolated from B. aegyptiaca ( L. )
Pharmacological Activities A more recent study was able to isolate the
Antidiabetic Activity: Different extracts of B. aegyptiaca subfraction-D from butanol fraction which exhibited the
(L.) Del show antidiabetic and hypoglycemic effects as highest inhibitory activity of aldose reductase enzyme
rported by many studies done to prove and understand (IC50 = 12.8±1 µg/ml) in B. aegyptiaca (L.) Del extract [80].
the possible mechanisms involved. The water extract of In the same context, a biologically active compound was
the mesocarp of fruits of B. aegyptiaca (L.) Del was isolated from the methanol extract (MeEx); 26-(O-b-D-
studied to possess lowering suger level effect in STZ- glucopyranosyl)-22-O-methylfurost-5-ene-3b,26-diol-3-O-
induced diabetic mice [71]. Similarly, ethyl acetate extract b-D-glucopyranosyl-(1 4)-[a-L-rhamnopyranosyl-(1
(EAE) from B.aegyptiaca (L.) Del has a defensive effect 2)]-b-D-glucopyranoside [81]. It showed a significant -
against oxidative stress induced by streptozocine with glucosidase and aldose reductase inhibitory effects
reduction in blood glucose levels, HbA1c, (IC50¼ 3.12 ± 0.17 and 1.04 ± 0.02 lg/mL, respectively)
malondialdehyde and vascular endothelial growth factor [81].
(VEGF) in diabetic retina [36]. The only randomized double-blinded (pilot) clinical
In same context, the bark extract has shown a study conducted till the present aimed to investigate the
reasonable effect on the activity of -amylase that is antidiabetic efficacy of the 70% ethanol extract of the
accountable for the decomposition of oligosaccharides pericarps of B.aegyptiaca ( L. ) Del with a nutritional
[72].Also, the fruit extracts (1.5 g/kg bw) decreased the intervention in elderly people [82]. It showed a reduction
level of the blood glucose by 24% with decreasing liver in both post prandial plasma glucose and fasting plasma
glucose-6-phosphatase activity extensively in diabetic glucose by 26.88% and 10.3%, respectively. This is a clear
infected rats. The aqueous and ethanolic extracts of B. evidence of the antidiabetic effect on humans.
aegyptiaca (L.) Del fruit induce significant reduction in In the same context, Artemisia sieversiana, medical
every component of diabetes which include serum herb widely distributed in China, has shown a similar anti-
glucose, glucagon, total lipids, total cholesterol, diabetic effects [83]. It exhibited a significant acute and
triglycerides level and transaminases [aspartate sustained hypoglycemic effects with decreasing plasma
aminotransferase (AST), alanine aminotransferase (ALT) lipid profiles induced by an insulin-like effect on glucose
and ãGT (gamma aminotransferase)] activities [73, 74]. transport [84, 85]. Similarly, Withania somnifera (L.) Dunal
In comparing to similar effects in other plants, the (Solanaceae), also known as ashwagandha, showed
roots of Panax ginseng or traditionally known as hypoglycemic and hypolipidemic activities with restoring
Korean ginseng have a great value in folk medicine all parameters of diabeti rats into normal euglycemic state
especially within East Asian countries, such as Japan, [86].
Korea and China for about 2000 years [75]. The roots of
Panax ginseng has been shown to improve insulin Anti-microbial Activity: The anti-microbial activity of
sensitivity and glucose homeostasis with reduction of different parts of B.aegyptiaca (L.) Del has been proven
blood glucose simulating the effect of an insulin sensitizer by many studies [87-89]. The leaf extracts done in water
[75, 76]. and organic solvents (acetone and ethanol) showed
52%; which is twice the activity of 100 nM insulin with
Del fruit [79].
Global J. Pharmacol., 12 (1): 01-12, 2018
6
antibacterial activity against Salmonella typhi. In paniculata (Burm.f) showed anti-microbial activity that
comparison of ethanolic extracts to water, the former effect various bacteria and fungi [94].
exhibited very high antibacterial activity (16 mm zone
of inhibition) than the later (4 mm zone of inhibition) at Anti-cancer Activity: Saponin extracted from B.
100 mg/ml. The preliminary phytochemical analysis aegyptiaca (L.) Del fruit showed anti-tumor activity.
revealed the presence of saponins, tannins, phenols and According to two studies –conducted in mice-, it reduced
anthraquinones which may explain the antibacterial the number of ehrlich ascites carcinoma (EAC) in both
activity [87]. therapeutic group and preventive groups with an increase
In the same perspective, flavonoid extracts of callus in life span compared to controls [95, 96].
tissue showed antimicrobial activity against; Escherichia In the same context, it showed anti-proliferative and
coli,Proteus vulgaris,Pseudomonas aureginosa, cytotoxic activity using various extracts as ethylacetae
Citrobacter amalonaticus,Staphylococcus aureus, extract, ethanol extract and chloroform with ethylacetae
Micrococcus lylae,Bacillus subtilis and Sporolacto extract being the most effective among them [97].
bacillus with higher activity against gram +ve bacteria Moreover, it also has anti-proliferative activity against
[88]. Active principles isolated were discovered as human foreskin fibroblast (HFF), MCF-7 human breast
flavonoids quercetin and kaempferol. Consequently, it can cancer cells and HT-29 human colon cancer cells with in
be concluded that antimicrobial activity of tissue culture vitro inhibition rates up to 82% [98]. Also, it showed anti-
extracts of B.aegyptiaca ( L. ) Del may be due to the proliferative activity in opposition to both HepG2 and
presence of these flavonoids in sufficient amount [88]. Caco2 cells with more prominent effect on HepG2 cells
In comparstion to similar effects in other plants,[99].
Saussure laniceps (Compositae), commonly known as Interestingly, when a mixture of balanitin-6 and -7
“cotton-headed snow lotus” have a great value in folk were used in mice bearing murine L1210 leukemia grafts,
medicine especially within East Tibetan and Chinese it increased their survival time and with a significant anti-
people [90]. Its extracts showed inhibitory effects against cancer activity [30]. Furthermore, methanol extract of B.
26 types of bacteria as well as pants' pathogenic fungi aegyptiaca (L.) Del stem bark acted as anti-tumor agent in
which mostly attributed to interactions with cell membrane mice injected with HCT-116 cells with significant
[90]. reduction in cancer cell growth [100].
Additionally, the hydroethanolic extracts of the bark
of B. aegyptiaca inhibited in vitro the growth of multi- Anti-oxidant Activity: The studies of different parts of
drug resistant Pseudomonas aeruginosa and B. aegyptiaca ( L. ) Del extracts has been reported to have
Staphylococcus aureus in a dose-dependent manner [91]. an anti-oxidant effects [101]. In addition, a raise in
Stem-barks of B. aegyptiaca (L.) Del contains antioxidant enzymes as superoxide dismutase and catalase
furanocoumarin-bergapten that showed anti-inflammatory, in mice treated with these extracts was an evident in
antioxidant and antimicrobial activities [7]. As comparison to control group [96].
furanocoumarins have a lactone structure, they have a Another study testified that methanol extract of B.
wide range of biological activity which may count for this aegyptiaca (L.) Del revealed the highest anti-oxidant
antimicrobial activity. A corresponding inhibitory activity activities while hexane and water extracts were with
of both methanolic and water extracts of whole plant unimportant activity. Also, it revealed a strong positive
extract on Staphylococcus aureus and Staphylococcus relation between total flavonoid and total phenolic
epidermidis has been documented by Parekh and Chanda contents and ferric reducing anti-oxidant power although
[89].Similarly, the crude extract of B.aegyptiaca (L.) Del a negative relation was found between both against Di
showed a significant reduction in bacterial growth in (pheny)-(2,4,6-trinitrophenyl) iminoazanium (DPPH) and
untreated well water [91, 92]. Phytochemical analysis 2,2-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid
disclose the occurrence of saponins, coumarins, (ABTS ) [100].
triterpenes, steroids and tannins which might be Moreover, it helps in scavenenging free radicals in
responsible for this activity [91]. diabetic patients and provide anti-oxidant protection as a
In the same context, the genus Garcin (family result of increasing endogenous production of anti-
Clusiaceae) is a medical herb widely distributed in India, oxidant agents [35]. Phenolic and flavonoid contents of
has shown a similar anti-microbial effects [93]. It exhibited B. aegyptiaca (L.) Del were found to be responsible for
a similar effect to clarithromycin. Similarly andrographis their anti-oxidant effect; both have redox properties that
Global J. Pharmacol., 12 (1): 01-12, 2018
7
allow them to act as hydrogen donors, single oxygen ACKNOWLEDGEMENTS
quenchers and reducing agents [100]. It also prevents
lipid oxidation in food thus inhibiting many diseases as
cancer and atherosclerosis [102]. According to some
reports, the anti-oxidant activity of desert date extract
is dose dependent with safety dose up to 1000 mg/kg
[95, 103].
Anti-viral Activity: Extract of B. aegyptiaca (L.) Del bark
aqueous is used to treat both acquired immune deficiency
syndrome (AIDS ) and leukemia. When this extract was
orally administrated for a month to AIDS patients, it
showed good results. The same was done with leukemia
patients, an increase in the stem bark extract was tested
against Herpes Simplex Virus, Coxsackie B2, Semliki forest
A7 and Vesicular stomatitis Virus, it gave negative
results with no activity on them as reported by Maregesi
et al. [104].
Anti-inflammatory Activity: It has been reported that
both methanol and butanol extracts of desert dates have
a significant anti-inflammatory effect on the rat paw edema
with respect to controls. Furthermore, methanol extract
had no dose-response relation, as both the lowest (200
mg/kg) and the highest (400 mg/kg) doses showed the
same effect on edema reduction. Although, butanol
extract showed a significant dose-response relation [105].
A study conducted on rats indicated that petroleum
and ethanolic extracts of aerial parts of desert dates have
a significant effect on carrageenan-induced hind paw
edema in comparison to the effect of the standard drugs
as control group, indomethacin and diclofenac sodium,
respectively. The same study reported that ethanol extract
had more significant effect on treating inflammatory
related pains [106].
CONCLUSION
Balanites aegyptiaca (L.) Del has been used in
folkloric remedy for a extensive period of time with several
and diverse uses [107-111]. Recently, numerous studies
reported that B. aegyptiaca (L.) Del has proved these
actions and activities as antidiabetic, antimicrobial,
antioxidant, anticancer, antiviral and anti-Inflammatory
activity as clearly mentioned [81, 83].
It is apparent that future studies are needed to
explore B. aegyptiaca (L.) Del utilization along with
pharmacological activites and possibility to cure and treat
different diseases both safely and effectively with better
understanding of the exact mechanisms of actions.
Thanks are due to Dr. A. EL Feel, Department of Arid
land Agriculture, Faculty of Meteorology, Environment
and Arid land Agriculture, King Abdulaziz University, for
his helpful discussions.
REFERENCES
1. Orwa, C., A. Mutua, R. Kindt, R. Jamnadass and
S. Anthony, 2009. Agroforestree Database: a tree
reference and selection guide; version 4.0. World
Agroforestry Centre, Kenya.
2. Sands, M.J.S., 2013. Flora of tropical East Africa:
Balanitaceae. In: Beentje H.J. (ed.) and Ghazanfar S.A.
(subed.), Flora of tropical East Africa, Royal Botanic
Gardens, Kew, pp: 1- 17.
3. Sagna, M.B., K.S. Niang, A. Guisse and D. Goffner,
2014. Balanites aegyptiaca (L.) Delile : distribution
géographique et connaissances ethnobotaniques des
populations locales du Ferlo (nord Sénégal). Biotech
Agro Soc Environ., 18: 503-511.
4. Arbonnier, M., 2004. Trees, shrubs and lianas of
West Africa Dry Zones.CIRAD, MARCRAF
Publishers; pp: 572.
5. Hall, J.B., 1992. Ecology of a key African
multipurpose tree species Balanites aegyptiaca Del.
(Balanitaceae): The state of knowledge. Forest Ecol
Manag. 50: 1-30.
6. Hines, D.A. and K. Eckman, 1993. Indigenous
multipurpose trees of Tanzania: Uses and economic
benefits for people; http:// www.fao.org/ docrep/
x5327e/ x5327e00.htm.
7. Chothani, D.L. and H.U. Vaghasiya, 2011. A review
on Balanites aegyptiaca Del (desert date):
phytochemical constituents, traditional uses and
pharmacological activity. Pharmacognosy Rev.,
5: 55-62.
8. Gardwtte, J. and M. Baba, 2013. FTIR and DSC
studies of the thermal and photochemical stability of
Balanites aegyptiaca oil (Toogga oil).Chem Phys
Lipids., 170(171): 1-7.
9. Elfeel, A.A., 2017. Changes in vapor pressure deficit
and air-to-leaf temperature difference due to the
effects of watering frequency and seasonal variation
induced adaptive responses in Balanites aegyptiaca.
Currr. Sci., 112(6): 1176-1182.
10. Elfeel, A.A. and E.I. Warrag, 2011.Uses and
conservation status of Balanites aegyptiaca (L.)Del.
(Hegleig Tree) in Sudan: Local people perspective.
Asian J agric Sci; 3(4) 386-390.
Global J. Pharmacol., 12 (1): 01-12, 2018
8
11. Gour, V.S. and T. Kant, 2012.Balanites aegyptiaca (L) 23. Chapagain, B.P. and Z. Wiesman, 2007. Determination
Del: a multipurpose and potential biodiesel tree
species of the arid regions. Int J Sci Nat; 3:472-475.
12. Kamel, M.S., K. Ohtani, T. Kurokawa, M.H. Assaf,
M.A. El-Shanawany, A.A. Ali, R. Kasai, S. Ishibashi
and O. Tanaka, 1991. Studies on Balanites aegyptiaca
fruits, an antidiabetic Egyptian folk medicine. Chem
Pharm Bull; 39: 1229-1233.
13. Okia, C.A., J.G. Agea, J.M. Kimondo,
R.A.A. Abohassan, P. Okiror, J. Obua and
Z.Teklehaimanot, 2011.Use and management of
Balanites aegyptiaca in Drylands of Uganda. Res J.
Biol Sci., 6(1): 15-24.
14. Kassa, H., K. Gebrehiwet and C. Yamoah, 2010.
Balanites aegyptiaca, a potential tree for parkland
agroforestry systems with sorghum in Northern
Ethiopia. J Soil Sci Environ Manage; 1(6): 107-114.
15. Gideon, P.K., 2013. Verinumber. The contribution of
Agroforestry tree product to rural farmers in Karim
Lamido Local Government. JFEWR; 5(1): 1-27.
16. Gad, M.Z., M.M. El-Sawalhi, M.F. Ismail and N.D. El-
Tanbouly, 2006. Biochemical study of the anti-
diabetic action of the Egyptian plants fenugreek and
balanites. Molcell biochem; 281: 173-183.
17. Katewa, S.S., B.L. Chaudhary and A. Jain, 2004. Folk
herbal medicines from tribal area of Rajasthan, India.
J. Ethnopharmacol; 92: 41-46.
18. Molla, E., M. Giday and B. Erko, 2013. Laboratory
assessment of the molluscicidal and cercariacidal
activities of Balanites aegyptiaca. Asian Pac J. Trop.
Biomed, 3(8): 657-662.
19. National Research Council, 2008. Lost Crops of
Africa: Volume III, Fruits, Development, Security and
Cooperation. The national Academies Press,
Washington, D.C.
20. Mohamed, A.M., W. Wolf and W.E. Spiess, 2002.
Physical, morphological and chemical characteristics,
oil recovery and fatty acid composition of Balanites
aegyptiaca Del. kernels. Plant Foods Hum Nutr
(Dordrecht, Netherlands); 57: 179-189.
21. Elfeel, A.A. and Z. Sherif, 2014. Hindi Balanites
aegyptiaca (L.) Del. var. aegyptiaca seed composition
and variability among three different intraspecific
sources. J. Life Sci., 11(7): 160-166.
22. Al Ashaal, H.A., A.A. Farghaly, M.M. Abd El Azizc
and M. Ali, 2010. Phytochemical investigation and
medicinal evaluation of fixed oil of Balanites
aegyptiaca fruits (Balantiaceae). J. Ethnopharmacol.,
127(2): 495-501.
of saponins in the kernel cake of Balanites
aegyptiaca by HPLC-ESI/MS. Phytochem Anal;
18: 354-362.
24. Manji, A.J., E.E. Sarah and U.U. Modibbo, 2013.
Studies on the potentials of Balanites aegyptiaca
seed oil as raw material for the production of liquid
cleansing agents. Int J. Phys. Sci., 8(33): 1655-1660.
25. Eromosele, I.C., C.O. Eromosele, A.O. Akintoye and
T.O. Komolafe, 1994. (Characterization of oils and
chemical analysis of the seeds of wild plants. Plant
Foods Hum Nutr., 46: 361-365.
26. Obidah, W., M.S. Nadro, G.O. Tiyafo and
A.U. Wurochekke, 2009. Toxicity of crude Balanites
aegyptiaca seed oil in rats. J Am Sci., 5(6): 13-165.
27. Chapagain, B.P., H. Yehoshua and Z. Wiesman, 2009.
Desert date (Balanites aegyptiaca) as an arid lands
sustainable bioresource for biodiesel. Bioresour
Technol., 100: 1221-1226.
28. Gutti, B., S. Kiman and A.M. Murtala, 2012. Solar
dryer - an effective tool for agricultural products
preservation. JATES, 2(1): 31-38.
29. Morkaz, M.G., K.M. Elamin, S.H. Ahmed and
S.A. Omer, 2011. Effects of feeding different levels of
Balanites aegyptiaca (HEGLIG) kernel cake on
cattle rumen environment. Online J. Anim. Feed Res.,
1(5): 209-213.
30. Gnoula, C., V. Mégalizzi and N. De, 2008. Nève
Sauvage S, Ribaucour F, Guissou P, Duez P, Dubois
J, Ingrassia L, Lefranc F, Kiss R, Mijatovic T.
Balanitin-6 and -7: Diosgenyl saponins isolated
from Balanites aegyptiaca Del. display significant
anti-tumor activity in vitro and in vivo. Int J. Oncol.,
32: 5-15.
31. Patil, S.V., B.K. Salunke, C.D. Patil, R.B. Salunkhe,
B. Gavit and V.L. Maheshwari, 2010. Potential of
extracts of the tropical plant Balanites aegyptiaca (L)
Del. (Balanitaceae) to control the mealy bug,
Maconellicoccus hirsutus (Homoptera:
Pseudococcidae). Crop Protection., 29: 1293-1296.
32. Dwivedi, A.V. Joshi, P.K. Barpete, A.K. Akhtar,
A. Kaur and S. Kumar, 2009. Anthelmintic activity
of root bark of Balanites aegyptiaca (L.) Del.
Ethnobotanical Leaflets., 13: 564-567.
33. Bukar, A., I.S. Danfillo, O.A. Adeleke and
E.O. Ogunbodede, 2004. Traditional oral health
practices among Kanuri women of Borno State,
Nigeria. Odontostomatol Trop., 107: 25-31.
Global J. Pharmacol., 12 (1): 01-12, 2018
9
34. Ojo, O.O., M.S. Nadra and I.O.Tella, 2006. Protection 45. Arbonnier, M., 2000. Arbres, arbustes et lianes des
of rats by extracts of some common Nigerian trees
against acetaminophen-induced hepatotoxicity. Afr
J Biotech;5: 755-760.
35. Abou Khalil, N.S., A.S. Abou-Elhamd, S.I. Wasfy,
M.H. Ibtisam, El Mileegy, Y.H. Mohamed and
M.A. Hussein, 2016.Antidiabetic and antioxidant
impacts of desert Date (Balanites aegyptiaca) and
Parsley (Petroselinum sativum) aqueous Extracts:
Lessons from experimental rats. J. Diabetes., 2016:
1-10.
36. Al-Malki, A.L., E.K. Barbour, K.O. Abulnaja and
S.S. Moselhy, 2015. Management of Hyperglycaemia
by Ethyl Acetate Extract of Balanites aegyptiaca
(Desert Date). Molecules (Basel, Switzerland);
20: 14425-14434.
37. Sands, M.J.S., 2001. The desert date and its relatives:
a revision of the genus Balanites. Kew Bulletin;
56(1): 1-128.
38. Hall, J.B. and D.H. Walker, 1991. Balanites
aegyptiaca; A monograph. School of Agricultural
and Forest Sciences Publication, University of
Wales.
39. Boesewinkel, F.D., 1994. Ovule and seed characters
of Balanites aegyptiaca and the classification of the
Linales- Geraniales - Polygalales assembly. Acta
Botanica Neerlandica; 43: 15-25.
40. Sheahan, M.C. and M.W. Chase, 2000. Phylogenetic
relationships within Zygophyllaceae Based on DNA
Sequences of Three Plastid Regions, with Special
Emphasis on Zygophylloideae. Syst Bot., 25(2): 371-
384.
41. Singh, K.K., M.M. Das, A.K. Samanta, S.S. Kundu
and S.D. Sharma, 2002. Evaluation of certain feed
resources for carbohydrate and protein fractions and
in situ digestion characteristics. Indian J. Anim Sci.,
72(9): 794-797.
42. National Plant Data Center, 2017. Natural Resources
Conservation Service National Plant Data Center N R
C S. https:// plants.usda.gov/ core/
profile?symbol=BAAE3.
43. Berhaut, J., 1979. La Flore illustrée du Sénégal. Préf.
de L. Sédar Senghor. J. Agric Trop Bot Appl;
21: 269-270.
44. Lebrun, J.P. and A.L. Stork, 1992. .Enumération des
plantes à fleurs d'Afrique tropicale. Volume II.
Chrysobalanaceae à Apiaceae, Conservatoire et
Jardin botaniques de la Ville de Genève, Genève,
Suisse.
zones sèches d’Afrique de l’Ouest. Montpellier,
France : CIRAD-MNHN-UICN.
46. Hamid, O.W.M. and E. Hassan, 2001. Balanites
aegyptiaca extract for treatment of HIV/ AIDS and
leukemia. International Publication Number WO
2001/49306 A.
47. Maksoud, S.A. and M.N.E. Hadidi, 1988. The
flavonoids of Balanites aegyptiaca (Balanitaceae)
from Egypt. Plant Syst and Evol., 160: 153-158.
48. Dawidar, A.A.M. and M.B.E. Fayez, 1969. Steroid
sapogenins—XIII. Phytochemistry, 8: 261-265.
49. Roland, H. and S. Ezekiel Abayomi, 1972. A
Reinvestigation of Balanites aegyptiaca as a source
of steroidal sapogenins. Econ Bot; 26: 169-173.
50. Varshney, I.P. and P. Vyas, 1982. Saponin and
sapogenin contents of Balanites roxburghii Int J.
Crude Drug Res., 20: 3-7.
51. Watt, J.M., B. Breyer and G. Maria, 1962. The
medicinal and poisonous plants of Southern and
Eastern Africa. London: Livingstone Ltd. 1 edition.
st
52. Varshncy, I.P. and D.C. Janin, 1979. Study of
glycosides from T. foenumgraccum L. leaves. Nad
Acad Sci Let (India); 2: 331-332.
53. Abu-El-Futuh, I., 1983. Balanites aegyptiaca, an
unutilized raw material potentially ready for agro-
industrial exploitation. United nations Industrial
Development Organization, Vienna, Austria report
UNIDO; 10-494.
54. Hosny, M., T. Khalifa, I. Çali , A.D. Wright and O.
Sticher, 1992.Balanitoside, a furostanol glycoside and
6-methyl-diosgenin from Balanites aegyptiaca.
Phytochemistry ; 31: 3565-3569.
55. Kamel, M.S., 1998. A furostanol saponin from fruits
of Balanites aegyptiaca. Phytochemistry; 48: 755-757.
56. Kamel, M.S. and A. Koskinen, 1995. Pregnane
glycosides from fruits of Balanites aegyptiaca.
Phytochemistry, 40: 1773-1775.
57. Staerk, D., B.P. Chapagain, T. Lindin, Z. Wiesman and
J.W. Jaroszewski, 2006. Structural analysis of
complex saponins of Balanites aegyptiaca by 800
MHz 1H NMR spectroscopy.Mol cell biochem;
44: 923-928.
58. Umar, K.J., L. Abubakar, B. Alhassan, S.D. Yahaya,
L.G. Hassan, N.A. Sani and M.U. Muhammad, 2014.
Nutritional profile of Balanites aegytptiaca flower.
Studia Universitatis “Vasile Goldi ”, Seria tiin ele
Vie ii; 24(1): 169-173.
Global J. Pharmacol., 12 (1): 01-12, 2018
10
59. Gaur, V.S.E.C., C.J. Emmanuel and T. Kant, 2005. 71. Mansour, H.A.N.A., 2000. Amelioration of impaired
Direct in vitro shoot morphogenesis in desert
date- B. aegyptaica (L.) Del. from root segments
multipurpose trees in the tropics: Management
and improvement strategies.In: Tewari VP,
Srivastava RL, editors. Jodhpur, Scientifc
Publication; 701-704.
60. Kheir, Y.M.E. and M.H. Salih, 1980. Investigations of
traditional herbal drugs as possible alpha amylase
inhibitors.Fitoterapia; 26: 271-274.
61. Liu, H.W. and K. Nakanishi, 1982. The structures of
balanitins, potent molluscicides isolated from
Balanites aegyptiaca. Tetrahedron ; 38: 513-519.
62. Hardman, R. and E.A. Sofowora, 1970. Isolation and
characterization of yamogenin from Balanites
aegyptiaca. Phytochemistry; 9: 645-649.
63. Saharan, V.Y.R. and Z. Wiesman, 2008. Balanites
aegyptiaca (L.) Delile: A potential source of saponin.
Current Biotica, 2: 110-113.
64. Farid, H., E. Haslinger, O. Kunert, Wegner and
M. Hamburger, 2002. New Steroidal glycosides from
Balanites aegyptiaca. Helv Chim Acta; 85: 1019-1026
65. Pettit, G.R., D.L. Doubek, D.L. Herald, A. Numata,
C. Takahasi, R. Fujiki and T. Miyamoto, 1991.
Isolation and structure of cytostatic steroidal
saponins from the African medicinal plant Balanites
aegyptica. J. Nat Prod; 54: 1491-1502.
66. Cordano, G.T.M., J. Plonsky, R.M. Rabanal and
P. Varenne, 1978. Balanitol, a new sesquiterpene from
B. roxburghii, carbon-13 NMR analysis of
eudesonance sesquiterpenoids. J. Indian Chem Soc.,
55: 1148-1151.
67. Sarker, S.D., B. Bartholomew and R.J. Nash, 2000.
Alkaloids from Balanites aegyptiaca. Fitoterapia,
71: 328-330.
68. Yadav, J.P. and M. Panghal, 2010. Balanites
aegyptiaca (L.) Del. (Hingot): A review of its
traditional uses, phytochemistry and pharmacological
properties. Int J Green Pharm; 4: 56-64.
69. Seifu, T., 2004. Ethnobotanical and
ethnopharmaceutical studies on medicinal plants of
Chifra District, Afar Region, North Eastern Ethiopia.
M. pharm, thesis, School of Graduate Studies of the
Addis Ababa University.
70. Gnoula, C.G.P., P. Duez, M. Frederich and J. Dubois,
2007. Nematocidal compounds from seeds of
Balanites aegyptiaca isolation and structure
elucidation. Int J. Pharm., 3: 280-284.
renal function associated with diabetes by Balanites
aegyptiaca fruits in streptozotocin-induced diabetic
rats. J Med Res Inst, 21: 115-125.
72. Funke, I.M.F. and C.W.Melzig, 2005.Phytotherapy in
type 2 diabetes mellitus. Investigations of traditional
herbal drugs as possible alpha amylase inhibitors.
Phytother Res; 26: 271-274.
73. Zaahkouk, S.A., H.M. Khalaf-Allah, S. Mehanna,
F.I. El-Gammal and A.F.Makkey, 2017.Studies on age,
growth and mortality rates for management of the
redspot emperor, Lethrinus lentjan (Lacepède, 1802)
in the Egyptian sector of Red Sea. Egy J. Aqua Biol.
Fish; 21: 63-72.
74. Baragob, A.E.A., W.H. AlMalki, I. Shahid,
F.A. Bakhdhar, H.S. Bafhaid and M.I.E. Omar, 2014.
The hypoglycemic effect of the aqueous extract of
the fruits of Balanites aegypticea in Alloxan-induced
diabetic rats. Pharmacognosy Res., 6: 1-5.
75. Park, J.D., D.K. Rhee and Y.H. Lee, 2005. Biological
activities and chemistry of saponins from Panax
ginseng C. A. Meyer. Phytochem Rev; 4: 159-175.
76. Chung, S.H., C.G. Choi and S.H. Park, 2001.
Comparisons between white ginseng radix and rootlet
for antidiabetic activity and mechanism in KKAy
mice. Arch Pharm Res., 24: 214-218.
77. Gad, M.Z., M.M. El-Sawalhi, M.F. Ismail and N.D. El-
Tanbouly, 2006. Biochemical study of the anti-
diabetic action of the Egyptian plants fenugreek and
balanites. Molcell biochem; 281: 173-183.
78. Motaal, A.A., S. Shaker and P.S. Haddad, 2012.
Antidiabetic activity of standardized extracts of
Balanites aegyptiaca fruits using cell-based
bioassays. Phcog., 4: 20-24.
79. Farag, M.A., A. Porzel and L.A. Wessjohann, 2015.
Unraveling the active hypoglycemic agent
trigonelline in Balanites aegyptiaca date fruit using
metabolite fingerprinting by NMR. J Pharm Biomed
Anal, 115: 383-387
80. Abdel Motaal, A., H. El-Askary, C.S. Olaf Kunert,
B. Sakr, S. Shaker, A. Grigore, R. Albulescu and
R. Bauer, 2015. Aldose reductase inhibition of a
saponin-rich fraction and new furostanol saponin
derivatives from Balanites aegyptiaca.
Phytomedicine; 22: 829-836.
81. Ezzat, S.M., A. Abdel Motaal and S.A.W. El Awdan,
2017. In vitro and In vivo antidiabetic potential of
extracts and a furostanol saponin from Balanites
aegyptiaca. Pharm Biol; 55: 1931-1936.
Global J. Pharmacol., 12 (1): 01-12, 2018
11
82. Rashad, H., F.M. Metwally, S.M.M. Ezzat, 92. Otieno, J.N.H.K. and H.V. Lyaruu, 2007. The effect of
S.A. Hasheesh and A.A. Motaal, 2017. Randomized
double-blinded pilot clinical study of the antidiabetic
activity of Balanites aegyptiaca and UPLC-ESI-
MS/MS identification of its metabolites. Pharm Biol;
55: 1954-1961.
83. Liu, S.J., Z.X. Liao, Z.S.Tang, C.L. Cui, H.B. Liu,
Y.N. Liang, Y. Zhang, H.X. Shi and Y.R. Liu, 2017.
Phytochemicals and biological activities of Artemisia
sieversiana. Phytochem Rev., 16: 441-460.
84. Niture, N.T., A.A. Ansari and S.R. Naik, 2014. Anti-
hyperglycemic activity of rutin in streptozotocin-
induced diabetic rats: an effect mediated through
cytokines, antioxidants and lipid biomarkers. Indian
J. Exp. Biol., 52: 720-727.
85. Ruiz-Aceituno, L., L. Ramos, I. Martinez-Castro and
M.L. Sanz, 2012. Low molecular weight carbohydrates
in pine nuts from Pinus pinea L. J. Agric Food Chem.,
60: 4957-4959.
86. Alam, N., M. Hossain, M.I. Khalil, M. Moniruzzaman,
S.A. Sulaiman and S.H. Gan, 2012. Recent advances
in elucidating the biological properties of Withania
somnifera and its potential role in health benefits.
Phytochem Rev., 11: 97-112.
87. Doughari, J.H.H., M.S. Pukuma and N. De, 2007.
Antibacterial effects of Balanites aegyptiaca L. Drel.
and Moringa oleifera Lam. on Salmonella typhi. Afr J.
Biotechnol; 6: 2212-2215.
88. Bidawat, S., R. Nag and T.N. Nag, 2011. Antimicrobial
principles from tissue cultures of Balanites
aegyptiaca. Biotechnol. Lett; 16: 6120-6124.
89. Parekh, J. and S. Chanda, 2007. In vitro screening of
antibacterial activity of aqueous and alcoholic
extracts of various Indian plant species against
selected pathogens from Enterobacteriaceae. Afr J.
Micro Res., 1: 92-99.
90. Chen, Q.L., X.Y. Chen, L. Zhu, H.B. Chen, H.M. Ho,
W.P. Yeung, Z.Z. Zhao and Y. Tao, 2016. Review on
Saussurea laniceps, a potent medicinal plant known
as “snow lotus”: botany, phytochemistry and
bioactivities. Phytochem Rev; 15: 537-565.
91. Anani, K., Y. Adjrah, Y. Ameyapoh, S.D. Karou,
A. Agbonon, C.S. de and M. Gbeassor, 2015. Effects
of hydroethanolic extracts of Balanites aegyptiaca
(L.) Delile (Balanitaceae) on some resistant
pathogens bacteria isolated from wounds.
Gbeassor, antimicrobial activities of Balanites
aegyptiaca (L.) Delile (i) on bacteria isolated from
water well., J. Ethnopharmacol., 164: 16-21.
local minerals Kadsaro towards the antimicrobial
activity of medicinal plants extract. Case of Lake
Victoria Basen, Tarim Tanzania. Afr J. Tradit
Complement Altern Med; 4: 1-6.
93. Hemshekhar, M., K. Sunitha, M.S. Santhosh,
S. Devaraja, K. Kemparaju, B.S. Vishwanath,
S.R. Niranjana and K.S. Girish, 2011. An overview on
genus garcinia: phytochemical and therapeutical
aspects. Phytochem Rev; 10: 325-351.
94. Subramanian, R., M. Zaini Asmawi and A. Sadikun,
2012. A bitter plant with a sweet future? A
comprehensive review of an oriental medicinal plant:
Andrographis paniculata. Phytochem Rev; 11: 39-75.
95. Al-Ghannam, S.M., H.H. Ahmed, N. Zein and
F. Zahran, 2013. Antitumor activity of balanitoside
extracted from Balanites aegyptiaca fruit. J. App.
Pharm Sci., 3: 179-191.
96. Issa, N.M., F.K. Mansour, F.A. El-Safti, H.Z. Nooh
and I.H. El-Sayed, 2015.Effect of Balanites aegyptiaca
on Ehrlich Ascitic carcinoma growth and metastasis
in Swiss mice. Exp Toxicol Pathol; 67: 35-441.
97. Al-Malki, A.L., E.K. Barbour, K.O. Abulnaja,
S.S. Moselhy, T.A. Kumosani and H. Choudhry,
2016. Balanites aegyptiaca protection against
proliferation of different cancer cell line. Afr J Tradit
Complement Altern Med., 13: 25-30.
98. Beit-Yannai, E., S. Ben-Shabat, N. Goldschmidt,
P. Bishnu, B. Chapagain, R.H. Liu and Z. Wiesman,
2011. Antiproliferative activity of steroidal saponins
from Balanites aegyptiaca - An in vitro study.
Phytochem Lett; 4: 43-47.
99. Yassin, A.M., N.M. El-Deeb, A.M. Metwaly, G.F. El
Fawal, M.M. Radwan and E.E. Hafez, 2017. Induction
of apoptosis in human cancer cells through extrinsic
and intrinsic pathways by Balanites aegyptiaca
Furostanol saponins and saponin-Coated silver
nanoparticles. App biochem biotech; 182: 1675-1693.
100. Hassan, L.E., S.S. Dahham, S.A. Saghir,
A.M. Mohammed, N.M. Eltayeb, A.M. Majid and
A.S. Majid, 2016. Chemotherapeutic potentials of the
stem bark of Balanite aegyptiaca (L.) Delile: an
antiangiogenic, antitumor and antioxidant agent.
BMC Complement Altern Med., 16(396): 1-13.
101. Meda, N.T., A. Lamien-Meda, M. Kiendrebeogo,
C.E. Lamien, A.Y. Coulibaly, J. Millogo-Rasolodimby
and O.G. Nacoulma, 2010. In vitro antioxidant,
xanthine oxidase and acetylcholinesterase inhibitory
activities of Balanites aegyptiaca (L.) Del.
(Balanitaceae). Pak J. of Biol. Sci., 13: 362-368.
Global J. Pharmacol., 12 (1): 01-12, 2018
12
102. Anselmi, C., F. Bernardi, M. Centini, E. Gaggelli, 107.Anto, F., M.E. Aryeetey, T. Anyorigiya, V. Asoala
N. Gaggelli, D. Valensin and G. Valensin, 2005. and J. Kpikpi, 2005. The relative susceptibilities of
Interaction of ferulic acid derivatives with human juvenile and adult Bulinus globosus and Bulinus
erythrocytes monitored by pulse field gradient NMR truncatus to the molluscicidal activities in the fruit of
diffusion and NMR relaxation studies. Chem Phys. Ghanaian, Blighia sapida, Blighia unijugata and
Lipids., 134: 109-117. Balanites aegyptiaca. Ann Trop Med Parasitol.,
103. Balakrishnan, B., S. Paramasivam and A. Arulkumar, 99: 211-217.
2014. Evaluation of the lemongrass plant 108. Gnoula, C.G.P., P. Duez, M. Frederich and J. Dubois,
(Cymbopogon citratus) extracted in different 2007. Nematocidal compounds from seeds of
solvents for antioxidant and antibacterial activity Balanites aegyptiaca Isolation and structure
against human pathogens. Asian Pac J. Trop. Dis., elucidation. Int J. Pharm., 3: 280-284.
4: S134-S139. 109. Koko, W.S., H.S. Abdalla, M. Galal and H.S. Khalid,
104. Maregesi, S.M., L. Pieters, O.D. Ngassapa, S. Apers, 2005. Evaluation of oral therapy on Mansonial
R. Vingerhoets, P. Cos, A. Dirk, V. Berghe and schistosomiasis using single dose of Balanites
A.J. Vlietinck, 2008. Screening of some Tanzanian aegyptiaca fruits and praziquantel. Fitoterapia.,
medicinal plants from Bunda district for antibacterial, 76: 30-34.
antifungal and antiviral activities. J. Ethnopharm., 110. Mohamed, A.H., K.E. Eltahir, M.B. Ali, M. Galal,
119: 58-66. I.A. Ayeed, S.I. Adam and O.A. Hamid, 1999. Some
105. Speroni, E., R. Cervellati, G. Innocenti, S. Costa, pharmacological and toxicological studies on
M.C. Guerra and A.S. Dall', 2005. Govoni P. Anti- Balanites aegyptiaca bark. Phyto Res; 13: 439-441.
inflammatory, anti-nociceptive and antioxidant 111.Shalaby, M.A., F.M. Moghazy, H.A. Shalaby and
activities of Balanites aegyptiaca (L.) Delile. Chem S.M. Nasr, 2010. Effect of methanolic extract of
Phys Lipids, 98: 117-125. Balanites aegyptiaca fruits on enteral and parenteral
106. Gaur, K.N.R., M.L. Kori, K.C.S. Sharma and stages of Trichinella spiralis in rats. Parasitol Res.,
S. Virendra, 2008. Antiinflammatory and analgesic 107: 17-25.
activity of Balanites aegyptiaca in experimental
animal models; Int J Green Pharma, 2: 214-217.
... This plant exhibited significant acute and sustained hypoglycemic effects with decreased plasma lipid profile induced by insulin like effect on glucose transport. [32][33] It showed moderate protein tyrosine phosphatase 1B inhibitory activity. [34] Anti-arthritic activity sieversiana which are found to be effective and common medicine used in Tibet so as to treat arthritis. ...
... [34] Anti-arthritic activity sieversiana which are found to be effective and common medicine used in Tibet so as to treat arthritis. [17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35] ...
Article
Full-text available
A. sieversiana is an annual or biennial herb belonging to family Asteraceae and is found in different countries like Korea, Northern Pakistan, Nepal, India (ladakh and Jammu & Kashmir), North and South Africa, Europe, Afghanistan, Tajikistan (Central Asia) and China. It is traditionally used to treat diarrhea, cold, detumescence, maintaining hemostasis, relieving heat and jaundice since ancient times. Among 66 chemical compounds reported in this plant, major constituents include flavonoids, steroids, alkaloids, lignans and terpenoids. These compounds could be an important therapeutic tool for development of new drugs for diabetes, cardiovascular, cancer and inflammation with more efficacy and lesser adverse effects. This article summarizes various pharmacological, phytochemical and toxicological results along with all the data concerning ethnopharmacology of plant and possibly determines its underlying curative properties.
... The plant grows as a thorny shrub to small tree and is being locally used for multiple utility especially for its medicinal value. The fruits, pulp, seed, leaves, bark and roots have antimicrobial, anticancer, antiviral, antidiabetic, antioxidant, anti-inflammatory and other properties used locally to cure many diseases such as jaundice, intestinal worm infection, wounds, malaria, syphilis, epilepsy, dysentery, constipation, diarrhea, hemorrhoid, stomach aches, asthma, and fever (Al-Thobaiti and Zeid, 2018;Saboo et al. 2014;Hammiche and Maiza, 2006). The leaves and fruits are used as a fodder for livestock (Orwa et al., 2009). ...
Article
Balanites roxburghii (Linn.) species has been classified under the category of endangered plant species due to excessive exploitation for a variety of purposes, which has necessitated conservation of this tree species, and hence a study was conducted to investigate the effect of potting mixture and sowing orientation on early growth performance and vigour. Seeds were subjected to seven potting mixtures: M1: Soil:Sand:FYM 2:1:1, M2: Soil:Cocopeat:FYM 2:1:1,M3: Soil:Cocopeat:Vermicompost 2:1:1, M4: Soil:Paddy Husk:FYM: 2:1:1, M5: Soil:Paddy Husk:Vermicompost: 2:1:1, M6: Soil: Saw Dust:FYM 2:1:1, and M7: Soil:sawdust: Vermicompost 2:1:1. The seeds were sown in three orientations. S1: Seeds laid vertically with stalk end downwards; S2: Seeds laid horizontally and S3: Seeds laid vertically with stalk end upwards. Physiological parameters considered for assessment were seed germination, days taken for germination, seedling length, and seedling vigor index. A completely randomized design was used for the experiment. The results showed that there is a significant difference among seven different potting mixtures and three orientations. At the end of 8 weeks, the seed is sown horizontally in the potting mixture Soil:cocopeat:vermicompost (2:1:1) has recorded the germination percentage of 71.67%, 37 days taken for seed germination, highest seedling length (64 cm), and highest seedling vigour index (4561). The high-vigor seedlings may survive even in unfavorable conditions, with high survival rate compared to others. The study recommended that to obtain high-vigor Balanites roxburghii seedlings, seeds may be sown in potting mixture soil: cocopeat: vermicompost (2:1:1) with horizontal orientation.
... Balanites Aegyptiaca is a perennial plant commonly utilised in food preparations, paticularlly in developing and most Africa countries. Balanites aegyptiaca, commonly known as the desert date, is an arid land tree valued for its diverse products and uses, including food, fodder, shade, oil, traditional medicine, and potential for use in shelterbelts and agroforestry systems (Al-Thobaiti and Abu Zeid, 2018). The fruit of the Balanites tree is particularly important, as it is edible and its seeds contain approximately 40%-87% oil (Kabo et al., 2020). ...
Article
Full-text available
In recent years, there has been an increasing focus on renewable and biodegradable energy sources among lubricant manufacturers due to the environmental impacts and limited availability of fossil-based engine oils. Biomass sources present a cost-effective and eco-friendly alternative to traditional mineral oil sources. This study aims to produce and characterize biodiesel and biolubricant from desert date seed oil through transesterification. The result of the study was compared with the properties of conventional and commercial lubricants. The study employed transesterification to convert desert date seed oil into biodiesel and biolubricant. The produced biolubricant and biodiesel were characterized to determine their kinematic viscosity at 40°C, specific gravity, flash point, and pour point. These properties were then compared with those of other bio-lubricants and commercial base lubricants. For biodiesel, the yield was 56%, with a favorable acid value (0.98 mg KOH/g), iodine value (43.41 mg/g), and saponification value (197.4 mg KOH/g). Although, the specific gravity (1.876) was higher than ASTM standard. However, the flash point (112°C) and cloud point (11°C) were within acceptable ranges. The biolubricant produced from desert date oil showed promising results with a high kinematic viscosity of 67.54 mm 2 /s, a specific gravity of 1.876, a flash point of 120°C and a pour point (−5°C). These results obviously suggest the produced lubricant a suitable for automotive applications possessing good low-temperature performance. The flash point result and the physicochemical properties of the oil aligned well with industrial standards. The comparisons revealed that the produced biolubricant closely matched the properties of SAE VG 220 and SAE VG 40. The findings suggest that the biolubricant and biodiesel derived from desert date seed oil can serve as a viable substitute for petroleum-based lubricants in light gear applications and can be effectively used in two-stroke engines, providing a sustainable alternative to conventional lubricants. CITATION Adeoti MO, Jamiru T, Adegbola TA, Abdullahi M, Sulaiman I and Aramide BP (2024), Comparative study on lubrication properties of biodiesel and bio-lubricant trans-esterified from desert seed oil with conventional lubricants.
... Balanites Aegyptiaca is a perennial plant commonly utilised in food preparations, paticularlly in developing and most Africa countries. Balanites aegyptiaca, commonly known as the desert date, is an arid land tree valued for its diverse products and uses, including food, fodder, shade, oil, traditional medicine, and potential for use in shelterbelts and agroforestry systems (Al-Thobaiti and Abu Zeid, 2018). The fruit of the Balanites tree is particularly important, as it is edible and its seeds contain approximately 40%-87% oil (Kabo et al., 2020). ...
... Balanites Aegyptiaca is a perennial plant commonly utilised in food preparations, paticularlly in developing and most Africa countries. Balanites aegyptiaca, commonly known as the desert date, is an arid land tree valued for its diverse products and uses, including food, fodder, shade, oil, traditional medicine, and potential for use in shelterbelts and agroforestry systems (Al-Thobaiti and Abu Zeid, 2018). The fruit of the Balanites tree is particularly important, as it is edible and its seeds contain approximately 40%-87% oil (Kabo et al., 2020). ...
Article
Full-text available
In recent years, there has been an increasing focus on renewable and biodegradable energy sources among lubricant manufacturers due to the environmental impacts and limited availability of fossil-based engine oils. Biomass sources present a cost-effective and eco-friendly alternative to traditional mineral oil sources. This study aims to produce and characterize biodiesel and biolubricant from desert date seed oil through transesterification. The result of the study was compared with the properties of conventional and commercial lubricants. The study employed transesterification to convert desert date seed oil into biodiesel and biolubricant. The produced biolubricant and biodiesel were characterized to determine their kinematic viscosity at 40°C, specific gravity, flash point, and pour point. These properties were then compared with those of other bio-lubricants and commercial base lubricants. For biodiesel, the yield was 56%, with a favorable acid value (0.98 mg KOH/g), iodine value (43.41 mg/g), and saponification value (197.4 mg KOH/g). Although, the specific gravity (1.876) was higher than ASTM standard. However, the flash point (112°C) and cloud point (11°C) were within acceptable ranges. The biolubricant produced from desert date oil showed promising results with a high kinematic viscosity of 67.54 mm ² /s, a specific gravity of 1.876, a flash point of 120°C and a pour point (−5°C). These results obviously suggest the produced lubricant a suitable for automotive applications possessing good low-temperature performance. The flash point result and the physicochemical properties of the oil aligned well with industrial standards. The comparisons revealed that the produced biolubricant closely matched the properties of SAE VG 220 and SAE VG 40. The findings suggest that the biolubricant and biodiesel derived from desert date seed oil can serve as a viable substitute for petroleum-based lubricants in light gear applications and can be effectively used in two-stroke engines, providing a sustainable alternative to conventional lubricants.
... M. stenopetala is native to east Africa, with diversity spanning Ethiopia, Kenya, and Central Somalia [19]. In Ethiopia, the distribution of the species is mostly concentrated in specific zones in the south [20][21][22][23]. ...
Chapter
Full-text available
Moringa stenopetala is a multipurpose tropical plant native to East Africa. The plant is exceptionally rich in nutrients and health-promoting bioactive compounds. It is among the top plants that could potentially feed the world and alleviate nutritional deficiencies. Moringa stenopetala is a versatile plant because its various parts, including leaves, seeds, flowers, pods, bark, and roots are useful to humans. Especially, the leaves and seeds are high in protein with all the essential amino acids. Based on the FAO database, M. stenopetala seed protein with its essential amino acid content stands highest among all commercial plant protein sources. Though it is a high-value plant and extensively used for food and traditional medicine by the local people in its native place, it is underutilized elsewhere. This chapter reviews recent research efforts that aim to unlock the potential of the plant as a source of ingredients for food, cosmetic and nutraceutical industries.
... The Balanites name originally derived from the Greek word which means fruit resemble acorn [1] and also known by different vernacular names in various countries. It is native to arid and sub arid part of Africa and Middle East especially Arabian Peninsula, but most widely in various parts of Africa and South Asia [2] . Balanites aegyptiaca L. is multipurpose plant used for food and fodder in different regions of Africa and South Asia [3] . ...
... The Balanites name originally derived from the Greek word which means fruit resemble acorn [1] and also known by different vernacular names in various countries. It is native to arid and sub arid part of Africa and Middle East especially Arabian Peninsula, but most widely in various parts of Africa and South Asia [2] . Balanites aegyptiaca Linn. ...
Article
Full-text available
Consumers’ growing awareness and desire for food free of pesticide residues led to the incubation of this research work. The study aimed at developing a nanoemulsion formulation of Balanite aegyptiaca seed kernel extract for use as a biopesticide. A preliminary study was carried out on the solubility and miscibility of surfactant, carrier, and deionized water utilizing the low-energy spontaneous emulsification method. Information from the study was then used to plot a ternary phase diagram (TPD) showing both the isotropic zone and the anisotropic zones, from which a point with a surfactant, oil, and water ratio (20:20:60) was selected from the isotropic zone for the formulation. The developed nanoemulsion was tested for stability and thermostability, and both results revealed the system was stable. Similarly, the physiochemical properties of the developed nanoemulsion system were characterized, and the results showed that the system revealed the following properties: mean particle size of 173.2±21.6, polydispersity index (PDI) of 0.403±0.038, surface tension of 32.53±0.71, viscosity of 37.33±0.67 mPas, and a pH of 4.92±0.02. The formulation appears homogeneous, clear, and transparent, which further indicates it’s a nanoemulsion formulation. Therefore, the nanoemulsion formulation of B. aegyptiaca seed kernel can serve as a safe and environmentally friendly substitute for synthetic pesticides in the management of plant diseases.
Article
Full-text available
_______________ Keywords: Lethrinus lentjan Age Growth mortality rate Red Sea Egypt Age, growth and mortality are very important parameters for rational exploitation and management of the fish population. Age, growth, mortality and exploitation rates were studied to assess the current status of the redspot emperor Lethrinus lentjan stock in the Egyptian sector of Red Sea. The study was based on a total of 943 specimens that collected during 2014 and 2015 with total length range of 11.5 to 50.7 cm. Results showed that, the maximum life span of L. lentjan in the Egyptian Red Sea was 6 years and age group one is the most frequent one forming up to 54% of the total catch. L. lentjan attains its highest growth in length at the end of the first year of life (24.45 cm) after which the annual increment in length decreases gradually with the further increase in age. The b-value of length-weight relationship was estimated at 3.03 indicating a tendency towards isometric growth. The composite coefficient "k c " and the relative condition factor "K n " were fluctuated according to different fish length groups and months. The length at first capture was L c = 20.11 cm with corresponding age T c = 0.58 year. The total mortality of L. lentjan (Z= 1.52/yr), natural mortality (M = 0.35/yr) and fishing mortality (F = 1.17/yr) were lead to an exploitation ratio of E = 0.77. The high values of both F and E are reflecting the high level of exploitation of this species in the Egyptian Red Sea waters.
Article
Full-text available
Context: Balanites aegyptiaca Del. (Zygophyllaceae) fruits are well-known antidiabetic drug in Egyptian folk medicine. Nevertheless, its mechanism of action is still unclear. Objectives: Searching for the possible mechanisms of action of the plant and identification of its bioactive compounds. Materials and methods: A bio-guided protocol based on the evaluation of α‐glucosidase (AG) and aldose reductase (AR) inhibitory activities was adopted to isolate the biologically active compounds from the methanol extract (MeEx). An in vivo antidiabetic study was conducted for the active extract, fraction and compound using streptozotocin-induced diabetic male albino Wistar rats at two dose levels (100 and 200 mg/kg.b/wt) for 2 weeks. Results: Three compounds were isolated and identified: a sterol, (1) stigmasterol-3-O-β-d-glucopyranoside; a pregnane glucoside, (2) pregn-5-ene-3β,16β,20(R)-trio1-3-O-β-d-glucopyranoside; a furostanol saponin, (3) 26-(O-β-d-glucopyranosyl)-22-O-methylfurost-5-ene-3β,26-diol-3-O-β-d-glucopyranosyl-(1 → 4)-[α-l-rhamnopyranosyl-(1 → 2)]-β-d-glucopyranoside. Only compound 3 possessed significant AG and AR inhibitory activities (IC50 = 3.12 ± 0.17 and 1.04 ± 0.02 μg/mL, respectively), while compounds 1 and 2 were inactive. The in vivo antidiabetic study revealed that MeEx and furostanol saponin 3 possessed significant activities at a dose of 200 mg/kg through reducing the fasting plasma glucose level by 46.14% and 51.39%, respectively, as well as reducing the total cholesterol by 24.44% and 31.90%, respectively. Compound 3 also caused increment in insulin and C-peptide levels by 63.56% and 65%, respectively. Discussion and conclusions: We presented a scientific base for using Balanites aegyptiaca, and shed the light on one of its saponins, as an antidiabetic agent in fasting and postprandial hyperglycaemia along with the improvement of diabetic complications.
Article
Full-text available
This study examines intraspecific variability among three sources (KSA, SD5.1 and SD6.2) of Balanites aegyptiaca in Saudi Arabia in their response to different watering frequencies and seasonal changes in vapour pressure deficit (VPD) and air-to-leaf temperature difference (∆T) under field condition. Irrigation was done once a week, once every two weeks or once every three weeks. Traits measured include: tree height, diameter (DM), relative monthly height (RMHI) and diameter (RMDI) increments, stomatal resistance (Rs), specific leaf weight (SLW). VPD and ∆T were measured during the same time of Rs and SLW measurements. Both Rs and SLW directly responded to irrigation treatment and seasonal variation in ∆T and VPD. Interactive effects of hot weather and water stress increased leaf temperature, resulting in less ∆T and more VPD that induced higher Rs and SLW values. SD5.1 accounted for better responses under water stress, due to its higher Rs and SLW in the same time maintained better growth. DM and RMDI were more responsive to watering stress and varied among the sources. Early seedlings root-toshoot ratio was associated with better growth performance later in the field. The results highlight the role of hot weather and water stress in producing large changes in ∆T and VPD that have a major impact on Rs and SLW. In addition, there is large intraspecific variation in field growth and adaptive responses among seeds brought from different provenances.
Article
Full-text available
The aim of this investigation is to examine the anticancer activities of Balanites aegyptiaca fruit extract with its biogenic silver nanoparticles (AgNPs) against colon and liver cancer cells. B. aegyptiaca aqueous extract was fractionated according to polarity and by biosynthesized AgNP. The cytotoxicity of the extract, semi-purified fractions, and the AgNPs was examined on noncancerous cell lines. The safer fraction was subjected to ultra-performance liquid chromatography-MS to identify the major active constituents. The anticancer activities of the nontoxic doses of all the used treatments were tested against HepG2 and CaCo2 cells. The nontoxic dose of the B. aegyptiaca (0.63 mg/ml) extract showed high anti-proliferative activities against HepG2 and CaCo2 with a percentage of 81 and 77%, respectively. The butanol fraction was safer than the other two fractions with 46.3 and 90.35% anti-proliferative activity against Caco2 and HepG2 cells, respectively. The nontoxic dose of AgNPs (0.63 mg/ml) inhibits both HepG2 and Caco2 cells with a percentage of 84.5 and 83.4%, respectively. In addition, AgNPs regulate the expression of certain genes with folding higher than that of crude extract. Saponin-coated AgNPs showed great abilities to select the most anticancer ingredient(s) from the B. aegyptiaca extract with a more safety pattern than the polarity gradient fractionation.
Article
Full-text available
Background Balanite aegyptiaca (L.) Delile, is a plant with extensive medicinal properties. Its stem bark is traditionally known for its spasmolytic and antiepileptic properties and used to treat yellow fever, jaundice and syphilis. Angiogenesis (sprouting of new blood vessels) is crucial for tumor growth and metastasis. The goal of this study is investigate the antiangiogenic, cytotoxicity and antioxidant activity as well as antitumor in vivo properties of B. aegyptiaca stem bark extracts. Method The dried powder of stem bark was extracted sequentially with n-hexane, chloroform, methanol and water. Rat aorta ring assay (RARA) was used as a platform to screen for antiangiogenic affect. The most active extract was subjected to further confirmatory antiangiogenic tests i.e. cell migration, tube formation and VEGF inhibition and finally evaluated for its in vivo antitumor efficacy in nude mice. The cytotoxicity of extracts on four cancer cell lines (HCT-116, K562, U937 and MCF-7) and one normal cells line (HUVEC) was evaluated. To assess the antioxidant activity screening, four methods were used, (DPPH•) and ABTS radical scavenging activity, as well as total flavonoids and phenolic contents. ResultsMethanol extract of B. aegyptiaca stem bark (MBA) showed the highest antiangiogenic, antioxidant and anticancer properties. It was found selectively cytotoxic to leukemia cell lines as well as breast cancer cell line MCF-7. (MBA) thus exhibited antiangiogenic in ex-vivo rat aorta ring model; it was found to excel its antiangiogenic effect via inhibition of the key growth factor (VEGF) as well as to halt HUVEC cell migration and tube formation, furthermore animals bearing colon cancer treated with (MBA) showed significant reduction in tumor growth. Conclusion Different extracts of B. aegyptiaca stem bark showed various anticancer and antiangiogenic properties. MBA demonstrated potent antiangiogenic, antioxidant and antitumor in vivo. The outcome of this study suggests the potential of stem bark of the B. aegyptiaca for developing chemotherapeutic agent against solid tumor as well as leukemia.
Article
Full-text available
This review discusses a whole plant’s chemical nature and biological effects of Artemisia sieversiana Ehrhart ex willd (ASS). Several types of chemical compositions have been isolated from A. sieversiana, including 26 terpenoids (21 guaiane-type sesquiterpenes, 3 germacrane-type sesquiterpenes, 1 muurolane-type sesquiterpene, and 1 diterpenoid), 16 sesamin-type lignans, 9 flavonoids, 3 steroids, and 3 alkaloids. Some of them have shown promising bioactivities, such as anti-tumour, anti-inflammatory, antioxidant functions and so on. Herein, we have summarized the phytochemical and pharmacological progress of ASS.
Article
Full-text available
Background: The aim of the present study was to evaluate in vivo anti-tumor activity of Balanites aegyptiaca fruits extracts in addition to its role in cell cycle and apoptosis.Materials and Methods: Antitumor activities of ethylacetae extract (EAE), ethanol extract (EE) and chloroform extract (CE) were tested against different cell line Hep-2, MCF-7, HL-60 and HCV29T. Calculation of the IC50 values for these extracts confirmed that the most potent plant extract was EAE (40 ug/ml) followed by EE (55ug/ml), CE (61ug/ml).Results: The ethanolic and chloroform extracts showed lower difference in their potency, while the EAE was found to be more active indicating for nonpolar active principles responsible for the anti-proliferative activity. The ethanolic extract was three times higher active than the chloroform extract. The results obtained showed that EAE exert a significant anti-proliferative, enhancement of apoptosis and modulation of cell cycle phases compared with vincristine.Conclusion: The presence of alkaloids, flavonoids and Phenolics increase its efficiency as anti-proliferative action. EAE has promising anti-cancer activity with higher activity than EE or CE extracts