Traditional Indian Medicines Used For The Management of Diabetes Mellitus
Traditional Indian Medicines Used For The Management of Diabetes Mellitus
Traditional Indian Medicines Used For The Management of Diabetes Mellitus
Correspondence
E mail: sirizvi@gmail.com
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Abstract
Plants have always been a source of drugs for humans since time immemorial. The Indian
traditional system of medicine is replete with use of plants for the management of
diabetic condition. According to World Health Organization, up to 90% of population in
developing countries use plants and its products as traditional medicine for primary
health care. There are about 800 plants which have been reported to show anti-diabetic
potential. The present review is aimed at providing in depth information about the anti
diabetic potential and bioactive compounds present in Ficus religiosa, Pterocarpus
marsupium, Gymnema sylvestre, Allium sativum, Eugenia jambolana, Momordica
charantia, and Trigonella foenum graecum. The review provides a starting point for
future studies aimed at isolation, purification and characterization of bioactive
antidiabetic compounds present in these plants.
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1. Introduction
Diabetes mellitus is a growing problem worldwide entailing enormous financial burden and
medical care policy issues [1]. According to International Diabetes Federation (IDF), the number
of individuals with diabetes in 2011 crossed 366 million, with an estimated 4.6 million deaths
each year [2]. The Indian subcontinent have emerged as the capital of this diabetes epidemic.
The reported prevalence of diabetes in adults between the ages of 20–79 years are: India 8.31%,
Bangladesh 9.85%, Nepal 3.03%, Sri Lanka 7.77% and Pakistan 6.72% [3].
Indians show a significantly higher age-related prevalence of diabetes when compared with
several other populations [4]. For a given BMI, Asian Indians display a higher insulin level
which is an indicator of peripheral insulin resistance. The insulin resistance in Indians is thought
to be due to their higher body fat percentage [5, 6]. Excess body fat, typical abdominal
deposition pattern, low muscle mass, and racial predisposition may explain the prevalence of
hyperinsulinemia and increased development of type 2 diabetes in Asian Indians.
The most common and effective antidiabetic medicinal plants of Indian origin are Babool
(Acacia Arabica), Bael (Aegle marmelose), Church Steeples (Agrimonia eupatoria), Onion
(Allium cepa),Garlic (Allium sativum), Ghritakumari (Aloe vera), Neem (Azadirachta indica),
Ash Gourd (Benincasa hispida), Beet root (Beta vulgaris), Fever nut (Caesalpinia bonducella),
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Bitter apple (Citrullus colocynthis), Ivy gourd (Coccinia indica), Eucalyptus (Eucalyptus
globules), banyan tree (Ficus bengalenesis), Gurmar (Gymnema sylvestre), Gurhal (Hibiscus
rosasinesis), Sweet potatoes (Ipomoea batatas), Purging Nut (Jatropha curcus), Mango
(Mangifera indica), Karela (Momordica charantia), Mulberry (Morus alba), Kiwach (Mucuna
pruriens), Tulsi (Ocimum sanctum), Bizasar (Pterocarpus marsupium), Anar (Punica granatum),
Jamun (Syzigium cumini), Giloy (Tinospora cordifolia), Methi (Trigonella foenum graecum). All
these plants are rich source of phytochemicals.
The present review presents the anti diabetic efficacy of some important plants used in traditional
system of medicine in India for the management of type 2 diabetes mellitus.
Decoction prepared from the bark is used in treatment of diabetes [13]. The plant is believed to
contain several bioactive principles including tannins, saponins, polyphenolic compounds,
flavonoids and sterols. Sitosteryl-d- glucoside present in the bark of Ficus religiosa is believed to
elicit hypoglycemic activity in rabbits [14]. The bioactive components present in Ficus are
Leucocyandin 3-O-beta-d-galactosyl cellobioside, leucopelargonidin-3- O-alpha-L rhamnoside
[15, 16]. The phytoconstituents present in ficus can impart significant antidiabetic effect. It has
been reported to contain phytosterols, flavonoids, tannins, furanocoumarin derivatives namely
bergapten and bergaptol [17].
The leaves of Ficus religiosa have also been studied for anti- hyperglycemic activity [18]. Oral
incorporation of aqueous extract of Ficus religiosa for 21 days caused a significant lowering in
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blood glucose levels and an elevated level of insulin has been observed. The skeletal muscle is
an important site for insulin-stimulated glucose uptake. Decrease in muscle and hepatic glycogen
in diabetes was observed to be corrected by peepal extract [19, 20].
Oxidative stress is one of the major etiologies in pathogenesis and complications of type 2
diabetes. F. religiosa has been reported to modulate the enzymes of antioxidant defence system
to combat oxidative stress. Restoration of glutathione and inhibition of malondialdehyde content
has shown the antioxidative property of Ficus religiosa [23].
Eugenia jambolana (Black plum or Jamun) belongs to the family Myrtaceae. The most
commonly used plant parts are seeds, leaves, fruits and bark. Eugenia jambolana is an evergreen
tropical tree of 8 to 15 m height, with smooth, glossy turpentine smelling leaves. The bark is
scaly gray and the trunk is forked. There are fragrant white flowers in branched clusters at stem
tips and purplish-black oval edible berries. The berries contain only one seed. The taste is
generally acid to fairly sweet but astringent. This tree is known to have grown in Indian sub-
continent and in other regions of South Asia such as, Nepal, Burma, Sri Lanka, Indonesia,
Pakistan and Bangladesh from ancient time.
Jamun has been reported to be used in numerous complementary and alternative medicine
systems of India and, before the discovery of insulin, was a frontline antidiabetic medication
even in Europe. The brew prepared by Jamun seeds in boiling water has been used in the various
traditional systems of medicine in India [24].
Eugenia jambolana is one of the widely used medicinal plants in the treatment of diabetes and
several other diseases. The plant is rich in compounds containing anthocyanins, glucoside,
ellagic acid, isoquercetin, kaemferol, myricetin and hydrolysable tannins (1-0- galloyl castalagin
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and casuarinin). The seeds also contain alkaloid jambosine and glycoside jamboline, which slows
down the diastatic conversion of starch into sugar [25].
The whole plant of Eugenia jambolana is reported to show antioxidative defence due to
numerous phytochemical constituents present in it. The bark of jamun is rich in several bioactive
compounds including quercetin, betulinic acid, B- sitosterol, eugenin, ellagic and gallic acid
[26], bergenin [27], tannins [28] and flavonoids. Fruits contain glucose, fructose, raffinose [29],
mallic acid [30] and anthocyanins [31], leaves are rich in acylated flavonolglycosides [32],
quercetin, myricetin and tannins [33] all of which have hypoglycemic ability.
The blood glucose lowering effect of Eugenia jambolana may be due to increased secretion of
insulin from the pancreas or by inhibition of insulin degradation [34]. Eugenia jambolana is
also reported to have lipid lowering effect evidenced by reduction of blood cholesterol,
triglycerides and free fatty acids [35]. This effect has been reported to be due to the presence of
flavonoids, saponins and glycoside in the extract which is reported to decrease the activity of
enzyme 3-HMG Co-A reductase in liver [36]. Eugenia jambolana seed extract is reported to
reduce blood pressure probably due to ellagic acid present in it [33].
Addition of ethanolic extract of seeds and seed powder of Eugenia jambolana in alloxan induced
diabetic rats showed significant reduction in blood sugar level and enhancement in
histopathology of pancreatic islets [37]. Decrease in glycosuria and blood urea levels has also
been reported. Similar kind of results has also been reported in numerous studies done on dogs
and rabbits [38, 39].
Eugenia jambolana fruit juice is diuretic and has been reported to provide soothing effect on
human digestive system [40]. The gastro-protective effect has also been reported in jamun seeds.
Elevation of antioxidant status and mucosal defensive properties might be the possible
mechanisms behind gastroprotective properties present in jamun. Presence of flavanoids in the
seeds provides the gastric ulcer protective activity to jamun [40]. Jamun shows antiviral activity
against goatpox and the highly pathogenic avian influenza (H5N1) virus [41,42].
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The efficacy of Eugenia jambolana has also been tested in pre clinical and clinical studies [43,
44] for hypolipidemic [45], antiinflammatory, [46], neuropsycho pharmacological [47], antiulcer,
[48], antibacterial [49], antiHIV [50], antidiarrhoeal [49] and antihypertensive activities [47].
Momordica charantia (Bitter gourd or Karela) belongs to the family Cucurbitacea. Fruit as a
whole and fruit seeds are the parts most frequently used for therapeutic benefits. Momordica
charantia is a popular fruit used for the treatment of diabetes, cardiovascular diseases and related
conditions amongst the indigenous population of Asia, South America and East Africa. It is often
used as a vegetable in diet. Bitter gourd contains bioactive substances with antidiabetic potential
such as vicine, charantin and triterpenoids along with some antioxidants [51]. Several pre-
clinical studies have documented the antidiabetic and hypoglycaemic effects of Momordica
charantia through various hypothesised mechanisms [52].
Several studies have demonstrated antibacterial, antiviral, anticancer and antidiabetic activities,
in Momordica charantia [53, 54] however, the anti-diabetic activity has been widely reviewed.
In several animal studies, bitter gourd has been reported to ameliorate metabolic syndrome,
where diabetes is one of the risk factors [55-57]. In a study conducted on Taiwanese adults, a
significant reduction in waist circumference, improvement in diabetes and symptoms of
metabolic syndrome, has been observed [58].
The hypoglycemic and lipid- lowering properties of bitter melon have been observed [59].
Studies have shown that Momordica charantia can repair damaged β-cells thereby stimulating
insulin levels [60], and also improve sensitivity/signalling of insulin [57]. Bitter gourd is also
reported to inhibit absorption of glucose by inhibiting glucosidase and suppressing the activity of
disaccharidases in the intestine [61].
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karela which could be responsible for activation of AMP -activated protein kinase [63]. The
blood glucose lowering activity of karela has been reported in several animal models [64].
Bitter melon is also effective in loosening adiposity. It is reported to decrease the weight of
epididymal and retroperitoneal white adipose tissues [54]. Bitter melon is found effective in
augmenting skeletal muscle strength, an effect which could be due to higher mRNA expression
for glucose transporter 4 [55]. Extracts/fractions of Antidesma madagascariense and Momordica
charantia were found to significantly inhibit the activity of α- glucosidase, a key carbohydrate
hydrolyzing enzyme. However, glycogen- loaded mice showed significant depressive effect on
increasing level of postprandial blood glucose after ingestion of Momordica charantia [65].
Presence of saponins to some extent might justify the inhibitory activities on α-amylase and α-
glucosidase. Saponins are also supposed to stimulate insulin secretion [66].
Ocimum sanctum L. (Holy basil or Tulsi) belongs to the family Lamiaceae. Every part of the
plant is used as therapeutic agent against several diseases. Ocimum (Holy basil) is reported to
grow world wide. Nutritional and Chemical composition of holy basil makes it a pla nt with
immense potential. Eugenol, the active constituent present in O. sanctum L. has been found to
be responsible for its therapeutic potential [67]. Major bioactive constituents present in the leaves
and stems of holy basil include flavonoids, saponins, tannins, triterpenoids, rosmarinic acid,
apigenin, isothymusin, isothymonin, cirsimaritin, orientin, vicenin. Tulsi leave oil contains
euginal, urosolic acid, carvacrol, linalool, limatrol, and caryophyllene along with eugenol. Seeds
oil is known to have fatty acids and sitosterol while seed mucilage contains some sugars.
Anthocyanins are present in green leaves. Furthermore, tulsi is also rich in vitamins, minerals,
chlorophyll and many other phytonutrients.
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30 days [71]. O. sanctum L. is reported to reduce the serum level of cortisol and glucose in male
mice showing its anti peroxidative effect [72].
Studies have reported that oral administration of alcoholic extract of leaves of O. sanctum L.
significantly reduced blood sugar level in normal, glucose-fed hyperglycemic and streptozotocin-
induced diabetic rats. Improvement in the action of exogenous insulin in normal rats has also
been recorded [73]. Mixed extract of P. marsupium and O. sanctum has been recorded to not
only rectify dyslipidemia but also in restoring the endogenous antioxidant levels in alloxan
induced diabetic rats [74].
Chloroform extracts of aerial parts of tulsi has been able to ameliorate the derangements in lipid
metabolism caused due to diabetes mellitus in alloxan induced diabetic rats. The extract
significantly decreased elevated level of serum glucose and also reversed the cholesterol,
triglyceride and LDL values [75].
The hydroalcoholic extract of O. sanctum L. given to stress induced male wister rats is reported
to significantly prevent the chronic-resistant stress induced rise in plasma cAMP level,
myocardial superoxide dismutase and catalase activities [76]. Urosolic acid isolated from O.
sanctum L. has been reported to protect heart cells from adriamycin induced lipid peroxidation
[77]. O. sanctum L is also used to control blood cholesterol. A marked decrease in serum
cholesterol, triacylglycerol and LDL + VLDL cholesterol as compared to untreated cholesterol-
fed group was observed in cholesterol- fed rabbits when supplemented with O. sanctum L. seed
oil for four weeks [78]. A similar kind of study performed on normal albino rabbits showed
lowered levels of serum total cholesterol, triglyceride, phospholipids and LDL-cholesterol and a
significant boost in the HDL-cholesterol and total fecal sterol contents with incorporation of
fresh leaves of tulsi [79].
Along with antidiabetic and cardioprotective effects, O. sanctum L. has also been suggested to
acquire antifungal [80], antimicrobial [81], analgesic [82], antihelmintic [83], antistress [9],
antifertility [84], antiinflammatory [85], antioxidant [78, 86], gastroprotective [87],
immunomodulatory [88], antithyroidic [89], anticancer [90], and radioprotective effects [91, 92].
Tulsi is reported to provide protection for central nervous system [93] and against sexually
transmitted diseases [94].
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2.5 Pterocarpus marsupium
Pterocarpus marsupium (Indian Kino tree, Bijasar) belongs to the family Fabaceae. Plant parts
used most commonly are heart wood, leaves, flowers, bark and gum. Pterocarpus marsupium
grows very well in India, Nepal and Sri Lanka. As per Ayurveda, it is one of the most versatile
medicinal plants with a wide spectrum of biological activities. Every part of the tree has been
acknowledged for its therapeutic potential. This tree grows up to 30 metres in height.
Compositional studies on bijasar have shown this plant to be a good source of polyphenols. P.
marsupium contains terpenoids and phenolic compounds: ß-sitosterol, lupenol, aurone
glycosides, epicatechins and iso- flavonoids [95, 96].
P. marsupium is known for its antidiabetic activity [97]. Besides eliciting a strong anti diabetic
property, Pterocarpus marsupium is reported effective against several diseases. It is reported to
be antiobesity, antihyperlipidemic [98], antiinflammatory, anthelmentic [99, 100], antioxidative,
antitumorigenic and antiulcerative [101, 71].
Pterocarpus marsupium is reported to have not only hypoglycemic property but also β-cell
protective and regenerative properties [102], effects which have been attributed to the flavonoid
content in the plant. Complete restoration of normal insulin secretion and regeneration of beta
cells has been reported in various experimental models of diabetes [103, 104]. A methanolic
extract of Pterocarpus marsupium when supplemented for 7 and 14 days to STZ-diabetic rats
showed normalization of streptozotocin-distressed serum glucose by correcting glycosylated
hemoglobin (HbA1c), serum protein, insulin, alkaline and acid phosphatase and albumin levels
[105].
The blood sugar lowering activity has been endorsed to be due to the presence of tannates in the
extract of the plant. Antihyperlipidemic activity is contributed probably due to the marsupin,
pterosupin and liquiritigenin present in the plant [106]. (−) Epicatechin has been shown to have
insulinogenic property by enhancing insulin release and conversion of proinsulin to insulin. (−)
Epicatechin has also been shown to possess insulin like activity [107, 108]. Epicatechin has also
been shown to strengthen the insulin signalling by activating key proteins of that pathway and
regulating glucose production through AKT and AMPK modulation in HepG2 cells [109].
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2.6 Trigonella foenum graecum
Trigonella foenum graecum (Fenugreek, Methi) belongs to the family Fabaceae. Seeds and
leaves are the most frequently used parts of the plant. Trigonella foenum-graecum L. (fenugreek)
is cultivated throughout India and in some other parts of the world as a semi-arid crop [80]. It is
used both as vegetable and as spice in India. Fenugreek is well known for its pungent aromatic
properties and is a flavoring agent in food [110]. Studies on different experimental models have
proved that fenugreek has strong antidiabetic properties [111, 112]. Human studies have also
confirmed the glucose and lipid-lowering ability of fenugreek [113].
Several studies have demonstrated that fenugreek seed extract, mucilage of seeds, and leaves can
decrease blood glucose and cholesterol levels in human and experimental diabetic animals [114,
115]. The therapeutic potential of fenugreek is primarily due to the presence of saponins [116],
4-hydroxyisoleucine [117], trigonelline, an alkaloid [118] and high- fiber content [119].
The antihyperglycemic effect has been correlated with decline in somatostatin and high plasma
glucagon levels [120]. Fenugreek seed powder has been shown to normalize the activity of
creatinine kinase in liver, skeletal muscles and heart of diabetic rats [121]. The anti-
hyperglycemic effect of fenugreek has been hypothesized to be due to the amino acid 4-
hydroxyisoleucine which acts by enhancement of insulin sensitivity and glucose uptake in
peripheral tissues [122]. The steroids present in methi have been reported to reduce blood
glucose level when supplemented to diabetic rats [123]. A considerable increment of the area of
insulin -immunoreactive β-cells has been observed [124].
A study on intestinal and renal disaccharidases activity in STZ induced diabetic rats proved the
beneficial effects of fenugreek seed mucilage by enhancing the reduction in maltase activity
during diabetes [125]. The optimistic influence of fenugreek supplementation on intestinal and
renal disaccharidases has been reported [126]. A marked reduction in renal toxicity has been
observed when fenugreek oil is incorporated in the diet of alloxanized rats [125].
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Gymnema sylvestre (Gurmar) belongs to the family Asclepiadaceae. It is a herb native to
the tropical forests of India and Sri Lanka. G. sylvestre is a large climber, with roots at nodes. It
is a potent antidiabetic plant used in ayurvedic preparations. Several studies have proved its anti-
diabetic potential in animal models [125], when combined with acarbose it is reported to reduce
intestinal transport of maltose in rats [127]. Absorption of free oleic acid in rats has also been
reduced [128].
Aqueous extract of G. sylvestre has been reported to cause reversible increases in intracellular
calcium and insulin secretion in mouse and human β-cells with type 2 diabetes [129].
Regeneration of the cells in the pancreas might raise insulin levels [130]. G. sylvestre can also
help prevent adrenal hormones from stimulating the liver to produce glucose in mice, thereby
reducing blood sugar levels [131]. A group of triterpene saponins, known as gymnemic acids and
gymnemosaponins are found present in G. sylvestre which are responsible for reported
pharmacological properties.
Allium sativum (Garlic) commonly called lahsun belongs to the family Amaryllidaceae. Leaves
and bulb are the parts frequently used. As per Ayurveda it is a miraculous plant used against a
variety of problems including, insect bites, intestinal worms, headache and tumors [140]. Garlic
is also used in folk medicine for the management of cardiac diseases, cancer, parasitic, fungal
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diseases and diabetes [141,142]. The principle bioactive components present in garlic are allicin,
allixin, ajoene and other organo-sulphur compounds.
Biological and therapeutic functions of garlic are basically due to the organo-sulphur
compounds they possess [143]. These chemical components are thought to exhibit numerous
biological effects including lowering of cholesterol and glucose, cancer prevention, and
antimicrobial properties [144]. Studies have proved that consumption of garlic significantly
decreased fasting blood sugar levels [145]. Diallyl trisulfide has been proved to improve
glycemic control in STZ- induced diabetic rats.[146] Incorporation of garlic juice resulted in
better utilization of glucose in glucose tolerance tests performed in rabbits, while allicin at a dose
of 250 mg/kg was 60% as effective as tolbutamide in alloxan- induced diabetic rabbits [147].
Garlic may act as an antidiabetic agent by increasing either the pancreatic secretion of insulin
from the β cells or release of bound insulin [148]. Allicin is supposed to enhance serum insulin
by combining with cysteine and sparing it from SH group reactions [147]. The beneficial effects
of N-acetylcysteine , an organosulfur from allium plants. on serum lipids and glucose are related
to its antioxidant property. N-Acetylcysteine is reported to reduce the oxidative stress by
improving the endogenous antioxidant defences [149].
Allicin, a sulfur-containing compound, is responsible for the pungent flavour and significant
hypoglycemic activity in garlic. This effect is supposed to be due to enhanced hepatic
metabolism, release of insulin and/or insulin sparing effect [150, 151]. S-allyl cystein sulfoxide
the precursor of allicin is reported to control lipid peroxidation and hyperglycemia in rats [152].
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80-97 % increment in the signs of hyperglycaemia and dyslipidaemia, 26-37 % increase in the
production of insulin and enrichment in the antioxidant defence system along with a 60-97 %
decrease in lipid peroxidation [158]. Administration of raw garlic homogenate was found to
normalise both hepatic TBARS and GSH levels and also improved insulin sensitivity and
oxidative stress in fructose- fed rats [159]. Numerous studies report that aged garlic extract inhibit
the generation of glycation -derived free radicals and AGEs in vitro. S -allyl cysteine, one of the
bioactive ingredients of aged garlic is a known antioxidant that possesses the capacity to inhibit
AGEs synthesis [160].
Conclusion
As per Ayurveda, there exist a huge collection of plants with antidiabetic potential. Only few of
them have been scientifically proven and a lot more have yet to be explored and proved. Ficus
religiosa, Gymnema sylvestre, Allium sativum, Trigonella foenum graecum, Pterocarpus
marsupium, Ocimum sanctum, Momordica charantia, Eugenia jambolana, Ficus religiosa have
shown varying degrees of hypoglycemic activity. These plants have also been reported to
contribute in control of complications of diabetes. Future studies may target on isolation,
purification and characterization of bioactive compounds present in these plants. The outcome of
such studies may provide a starting point for development of potential anti diabetic drugs. This
review may be helpful in the management of diabetes.
Conflict of Interests
References
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2. Hui Dong, NanWang, Li Zhao and Fuer Lu, “Berberine in the Treatment of Type 2
Diabetes Mellitus: A Systemic Review and Meta-Analysis,” Evidence-Based
Complementary and Alternative Medicine, vol. 2012, 2012.
3. N. Unwin, D. Whiting, L. Guariguata, G. Ghyoot and D. Gan, “IDF. Diabetes Atlas”, 5th
edition. eds. Brussels, Belgium: International Diabetes Federation, 2011.
4. M.K. Ali, K.M. Narayan and N. Tandon, “Diabetes and coronary heart disease: current
perspectives,” Indian Journal of Medical Research, vol. 132, pp. 584-597, 2010.
5. B.A. Banerji, N. Faridi, A. Rajesh, R.L. Chaiken and H.E. Lebovitz, “Body composition,
visceral fat, leptin and insulin resistance in Asian Indian men,” Journal of Clinical
Endocrinology Metabolism, vol.84, no. 1, pp. 137-144, 1999.
6. V. Dudeja, A. Misra, R.M. Pandey, G. Devina, G. Kumar a nd N.K Vikram, “BMI does
not accurately predict overweight in Asian Indians in northern India,” British journal of
Nutritionr, vol. 86, pp. 105–112, 2001.
8. World Health Organization, “Traditional medicine- growing needs and potential,” WHO
Policy Perspective on Medicines, vol. 2, pp. 1-6, 2002.
10. Asian Pacific Journal of Tropical Biomedicine, vol. 1, no. 2, pp. S291-S298, Abstract,
2011.
11. M. Simmonds and M.Howes, “Plants used in the treatment of diabetes,” In: Soumyanath,
A. (Ed.), Traditional Medicines for Modern Time – Antidiabetic Plants, 6th volume. CRC
Press/Taylor and Francis Group, pp. 19–82, 2006.
15
12. D. Singh, B. Singh and R.K. Goel, “ Traditional uses, phytochemistry and pharmacology
of Ficus religiosa: a review,” Journal of Ethnopharmacoogyl, vol. 134, no. 3, pp. 565-83,
2011.
14. S. Ambike and M. Rao, “Studies on a phytosterolin fromthe bark of Ficus religiosa,”
15. M. Bnouham, A. Ziyyat, H. Mekhfi, A. Tahri and A. Legssyer, “ Medicinal plants with
potential antidiabetic activity-a review of ten years of herbal medicine research (1990-
2000),” International Journal of Diabetes Metabolism, vol. 14, pp. 1-25, 2006.
17. K. D. Swami and N.P.S. Bisht, “Constituents of Ficus Religiosa and Ficus infectoria and
their biological activity,” Journal of Indian Chemical Society, vol. 73, pp. 631, 1996.
19. C. Bouche, S. Serdy, R. Kahn and A. Goldfine, “The cellular fate of glucose and its
relevance in Type 2 diabetes,” Endocrine Reviews, vol. 25, pp. 807–830, 2004.
20. J. Grover, V. Vats and S. Yadav, “Effect of feeding aqueous extract of Pterocarpus
metabolism,” Molecular and Cellular Biochemistry, vol. 241, pp. 53–59, 2002.
Gymnema montanum leaves on serum and tissue lipids in alloxan diabetic rats,”
16
22. M. Gayathri and K. Kannabiran, “Antidiabetic and ameliorative potential of Ficus
bengalensis bark extract in streptozotocin induced diabetic rats,” Indian Journal of
Clinical Biochemistry, vol. 23, no. 4, pp. 394-400, 2008.
23. H. Kirana , S.S. Agrawal , B.P. Srinivasan, “ Aqueous extract of Ficus religiosa linn.
reduces oxidative stress in experimentally induced type 2 diabetic rats,” Indian Journal of
experimental Biology, vol. 47, no. 10, pp. 822-6, 2009.
25. M. Ayyanar and P. Subash-Babu, “Syzygium cumini (L.) Skeels: A review of its
phytochemical constituents and traditional uses,” Asia Pacific Journal of Tropical and
Biomedicine, pp. 240-246, 2012.
26. N. Chaudhuri, A.K. Pal, S. Gomes and A. Bhattacharya, “Anti- inflammatory and related
action of Syzygium cumini seed extract,” Phytotherapy Research, vol. 4, no. 1, pp. 5-10,
1990.
27. I.S. Bhatia and K.L. Bajaj, “Chemical constituents of the seeds and bark of Syzygium
cumini” Planta Med, vol. 28, pp. 347-352, 1975.
29. Y.S. Lewis, C.T. Dwarakanath and D.S. Johar, “Acids and sugars in Eugenia
jambolana,” Journal of Scientific and Industrial Research,, vol. 15C, pp. 280-281, 1956.
31. J.K. Grover , V. Vats and S. Rathi, “ Anti- hyperglycemic effect of Eugenia jambolana
and Tnospora cordifolia in experimental diabetes and their effects on key metabolic
17
enzymes involved in carbohydrate metabolism,” Journal Ethnopharmacology, vol. 73,
no. 3, pp. 461-470, 2000.
33. Morton J, “Fruits of warm climates,” Miami: Julia Morton Winterville North Carolina,
1987.
34. M.J. Aybar, A.N.S. Riera, A. Grau and S. S. Sanchez, “Hypoglycemic effect of the water
extract of Smallantus sonchifolius (yacon) leaves in normal and diabetic rats,” Journal of
Ethnopharmacology, vol.74, pp. 125-132, 2001.
35. H. Sagrawat, A.S. Mann and M.D. Kharya, “Pharmacological potential of Eugenia
jambolana: a review,” Pharmacognosy Magazine, vol.2, no. 6, pp. 96–105, 2006.
37. N. Singh and M. Gupta, “Effects of ethanolic extract of Syzygium cumini (Linn) on
pancreatic islets of alloxan diabetic rats,” Indian Journal of Experimental Biology, vol.
45, pp. 861-867, 2007.
39. P. Kedar and C. H. Chakrabarti, “ Effects of Jambolana seed treatment on blood sugar,
lipids and urea in streptozotocin induced diabetes in rabbits,” Indian Journal of
Physiology and Pharmacology, vol. 27, no. 2, pp. 135, 1983.
43. S.B. Sharma, A. Nasir, K.M. Prabhu, P.S. Murthy and G. Dev, “ Hypoglycemic and
hypolipedimic effects of ethanolic extract of seeds of Eugenia jambolana in
alloxan induced diabetic rabbits,” Journal of Ethnopharmacology , vol. 85, pp. 201-
206, 2003.
44. L. Kopanski and G. Schnelle, “Isolation of bergenin from barks of Syzygium cumini,”
Planta Med, vol. 54, pp. 572, 1988.
46. A. Chaturvedi, G. Bhawani, P.K. Agarwal, S. Goel, A. Singh and R.K. Goel,
“Antidiabetic and antiulcer effects of extract of Eugenia jambolana seed in mild
diabetic rats: Study on gastric mucosal offensive acid-pepsin secretion,” Indian
Journal of Physiology and Pharmacology, vol. 53, no. 2, pp. 137-146, 2009.
47. M.A. Bhuiyan, My. Mia and M.A. Rashid, “Antibacterial principles of the seeds of
Eugenia jambolana,” Bangladesh Journal of Biology, vol. 25, pp. 239-241, 1996.
49. G. Indira and R. Mohan, “Jamun Fruits,” National Institute of Nutrition. ICMR,
Hyderabad, pp. 34-37, 1993.
19
50. R.T. Cirqueira and M.J.Q.F. Alves, “Hypotensive and diuretic effects of pitanga (Eugenia
uniflora L.) and jambos (Eugenia jambolana Lam.) aqueous extracts in normotensive
anesthetized rats,” Review of Brazilian Plants and Medicine, vol. 7, no. 2, pp. 86-91,
2005.
51. M.B. Krawinkel and GB Keding, “ Bitter gourd (Momordica charantia): A dietary
approach to hyperglycemia,” Nutritional Reviews, vol. 64, no. 7 Pt 1, pp. 331-337, 2006.
54. E. Basch, S. Gabardi and C. Ulbricht, “Bitter melon (Momordica charantia): A review of
efficacy and safety,” American Journal of Health System and Pharmmacy, vol. 60, pp.
356-359, 2003.
56. C.C. Shih, C.H. Lin, W.L. Lin and J.B. Wu, “Momordica charantia extract on insulin
resistance and the skeletal muscle GLUT4 protein in fructose- fed rats,” Journal of
Ethnopharmacology, vol. 123, pp. 82-90, 2009.
57. Z.Q. Wang, X.H. Zhang, Y. Yu, A. Poulev, D. Ribnicky, Z.E. Floyd, and W.T. Cefalu, “
Bioactives from bitter melon enhance insulin signaling and modulate acyl carnitine
content in skeletal muscle in high- fat diet- fed mice,” Journal of Nutritional Biochemistry
,vol. 22, pp. 1064-1073, 2011.
58. T. Chung-Huang, C. Emily Chin-Fun, T. Hsin-Sheng and H. Ching- jang, “Wild bitter
gourd improves metabolic syndrome: A preliminary dietary supplementation trial,”
Nutritional Journal, vol. 11, pp. 4-10, 2012.
20
59. Inayat-ur-Rahman, S.A. Malik , M. Bashir , R. Khan and M. Iqbal, “Serum sialic acid
changes in non- insulin-dependant diabetes mellitus (NIDDM) patients following bitter
melon (Momordica charantia) and rosiglitazone (Avandia) treatment,” Phytomedicine ,
vol. 16, no. 5, pp. 401-405, 2009.
60. A. Saxena and N.K. Vikram, “ Role of selected Indian plants in management of type 2
diabetes: a review,” Journal of Alternative and Complementary Medicine, vol. 10, no. 2,
pp. 369-378, 2004.
62. B.A. Shabib, L.A. Khan and R. Rahman, “Hypoglycemic activity of Coccinia indica and
Momordica charantia in diabetic rats: Depression of the hepatic gluconeogenic enzymes
glucose-6-phosphatase and fructose-1, 6-biphosphatase and elevation of liver and red-cell
shunt enzyme glucose-6-phosphate dehydrogenase,” Biochemical Journal, vol. 292, pp.
267–270, 1993.
63. H.L. Cheng, H.K. Huang, C.I. Chang, C.P. Tsai and C.H. Chou, “A cell-based screening
identifies compounds from the stem of Momordica charantia that overcome insulin
resistance and activate AMP-activated protein kinase,” Journal of Agriculture and Food
Chemistry, vol. 56, pp. 6835–6843, 2008.
64. Z.A. Malik , M. Singh and P.L.Sharma, “ Neuroprotective effect of Momordica charantia
in global cerebral ischemia and reperfusion induced neuronal damage in diabetic mice,”
Journal of Ethnopharmacology, vol. 133, no. 2, pp. 729-734, 2011.
66. Amy C. Keller, Jun Ma, A. Kavalier, Kan He, A. B. Brillantes, and E. J. Kennelly,
“Saponins from the traditional medicinal plant Momordica charantia stimulate insulin
secretion in vitro,” Phytomedicine, vol. 19, no. 1, pp. 32–37,2011 .
21
67. P. Pattanayak, P. Behera, D. Das and S.K. Panda, “Ocimum sanctum Linn. A reservoir
plant for therapeutic applications: An overview,” International Pharmacognosy Review,
vol. 4, no. 7, pp. 95–105, 2010.
68. V. Khan, A.K. Najmi, M. Akhtar, M. Aqil, M. Mujeeb and K.K. Pillai, “ A
pharmacological appraisal of medicinal plants with antidiabetic potential,” Journal
Pharmacy and Bioallied Sciences, vol. 4, no. 1, pp. 27–42, 2012.
70. J.M. Hannan, L. Marenah, L. Ali, B. Rokeya, P.R. Flatt and Y.H. Abdel-Wahab,
“Ocimum sanctum leaf extracts stimulate insulin secretion from perfused pancreas,
isolated islets and clonal pancreatic beta-cells,” Journal of Endocrinology, vol. 189, pp.
127–136, 2006.
71. R. Nair, T. Kalariya and S. Chanda, “Antibacterial activity of some selected Indian
medicinal flora,” Turkish Journal of Biology, vol. 29, pp. 41-47, 2005.
72. S. Gholap and A. Kar, “Hypoglycemic effects of some plant extracts are possibly
mediated through inhibition in corticosteroid concentration,” Pharmazie, vol. 59, pp.,
876–888, 2004.
73. R.R. Chattopadhyay, “Hypoglycemic effect of Ocimum sanctum leaf extract in normal
and streptozotocin diabetic rats,” Indian Journal of Experimental Biology, vol. 31, pp.
891–893,1993.
74. P.K. Singh , D. Baxi , S. Banerjee and A.V. Ramachandran , “Therapy with methanolic
extract of Pterocarpus marsupium Roxb and Ocimum sanctum Linn reverses dyslipidemia
and oxidative stress in alloxan induced type I diabetic rat model,” Experimental
Toxicology and Pathology, vol. 64, no. 5, pp. 441-448, 2012.
75. R.N. Patil , R.Y. Patil , B. Ahirwar and D. Ahirwar, “ Evaluation of antidiabetic and
related actions of some Indian medicinal plants in diabetic rats,” Asian Pacific Journal of
Tropical Medicine, vol. 4, no. 1, pp. 20-23, 2011.
76. S Sood, D Narang, MK Thomas, YK Gupta and SK Maulik, “Effect of Ocimum sanctum
Linn. on cardiac changes in rats subjected to chronic restraint stress,” Journal of
Ethnopharmacology, vol. 108, pp. 423–427, 2006.
77. S Balanehru and B Nagarajan, “Intervention of adriamycin induced free radical damage,”
Biochemistry International, vol. 28, pp. 735–744, 1992.
22
78. M.T. Trevisan, M.G. Vasconcelos Silva, B. Pfundstein, B. Spiegelhalder and R.W.
Owen, “ Characterization of the volatile pattern and antioxidant capacity of essential oils
from different species of the genus Ocimum,” Journal of Agriculture and Food
Chemistry, vol. 54, pp. 4378–4382, 2006.
79. A. Sarkar, S.C. Lavania, D.N. Pandey and C. Pant, “ Changes in the blood lipid profile
after administration of Ocimum sanctum (Tulsi) leaves in the normal albino rabbits,”
Indian Journal of Physiology and Pharmacology, vol. 38, pp. 311–312, 1994.
82. N. Khanna and J. Bhatia, “Antinociceptive action of Ocimum sanctum (Tulsi) in mice:
Possible mechanisms involved,” Journal of Ethnopharmacology, vol. 88, pp. 293–296,
2003.
83. M.K. Asha, D. Prashanth, B. Murali, R. Padmaja and A. Amit, “Anthelmintic activity of
essential oil of Ocimum sanctum and eugenol,” Fitoterapia, vol. 72, pp. 669–670, 2001.
84. M. Ahmed, R.N. Ahmed, R.H. Aladakatti and M.G. Ghosesawar, “ Reversible anti-
fertility effect of benzene extract of Ocimum sanctum leaves on sperm parameters and
fructose content in rats,” Journal of Basic and Clinical Physiology Pharmacology, vol.
13, pp. 51–59, 2002.
85. M.A. Kelm, M.G. Nair, G.M. Stasburg and D.L. DeWitt, “Antioxidant and
cyclooxygenase inhibitiory phenolic compounds from Ocimum sanctum Linn,”
Phytomedicine, vol. 7, pp. 7–13, 2000.
86. S.U. Yanpallewar, S. Rai, M. Kumar and S.B. Acharya. Evaluation of antioxidant and
neuroprotective effect of Ocimum sanctum on transient cerebral ischemia and long-term
cerebral hypoperfusion,” Pharmacology and Biochemical Behaviour, vol. 79, pp. 155–
164, 2004.
87. R.K. Goel, K. Sairam, M. Dorababu, T. Prabha and ChV. Rao’ “Effect of standardized
extract of Ocimum sanctum Linn. on gastric mucosal offensive and defensive factors,”
Indian Journal of Experimental Biology, vol. 43, pp. 715–721, 2005.
23
88. R. Mukherjee, P.K. Dash and G.C. Ram, “Immunotherapeutic potential of Ocimum
sanctum (L) in bovine subclinical mastitis,” Research in Veterinary Sciences, vol. 79, pp.
37–43, 2005.
89. S. Panda and A. Kar, “Ocimum sanctum leaf extract in the regulation of thyroid function
in the male mouse,” Pharmacology Research, vol. 38, pp. 107–110, 1998.
90. J. Prakash and S.K. Gupta, “Chemopreventive activity of Ocimum sanctum seed oil,”
Journal of Ethnopharmacology, vol. 72, pp. 29–34, 2000.
91. U.S. Bhartiya, Y.S. Raut and L.J. Joseph, “Protective effect of Ocimum sanctum L after
high-dose 131iodine exposure in mice: An in vivo study,” Indian Journal of
Experimental Biology, vol.44, pp. 647–652, 2006.
93. H. Joshi and M. Parle, “Evaluation of nootropic potential of Ocimum sanctum Linn.in
mice,” Indian Journal of Experimental Biology, vol. 44, pp. 133–136, 2006.
94. P. Shokeen, K. Ray, M. Bala and V. Tondon, “Prelimnary studies on activity of Ocimum
sanctum, Drynaria quercifolia and Annona squamosa against Neisseria gonorrohoeae.
Sexually Transmitted Diseases,” vol. 32, pp. 106–111, 2005.
95. J. Mitra and T. Joshi, “Isoflavonoids from the heart wood of Pterocarpus marsupiam”
Phytochemistry, vol. 22, pp. 2326-2327, 1983.
96. N. Kumar and T.R. Seshadri, “A new triterpene from Pterocarpus santalinus bark,”
Phytochemistry, vol. 9, pp. 1877-1878, 1976.
97. R.B. Kameswara, R. Guiri, M.M. Kesavulu and C.H. Apparao, “ Effect of oral
administration of bark extracts of Pterocarpus santalinus L. on blood glucose level in
experimental animals,” Journal of Ethnopharmacology, vol. 74, pp. 69 -74, 2001.
98. H.R. Ambujakshi and S. Ganapaty, “Anti obese activity of Pterocarpus marsupium barks
extract in experimentally induced obese rats,” Inventi Impact: Nutraceuticals 2011.
99. S. Hougee, J. Faber, A. Sanders, M.A. Hoijer and H.F. Smit, “Selective COX-2 inhibition
by a Pterocarpus marsupium extract characterized by pterostilbene and its activity in
healthy human volunteers,” Planta Med, vol. 7, pp. 387-392, 2005.
24
100. V.R. Salunkhe, A.V. Yadav, A.S. Shete, S.R. Kane and A.S. Kulkarni,
“Antiinflammatory acitivity of hydrogels of extracts of Pterocarpus marsupium and
Coccinia indica,” Indian Drugs, vol. 42, pp. 319-321, 2005.
101. J.K. Grover, V. Vats and S.S. Yadav, “Pterocarpus marsupium extract (Vijayasar)
prevented the alteration in metabolic patterns induced in the normal rat by feeding an
adequate diet containing fructose as sole carbohydrate,” Diabetes Obesity and
Metabolism, vol7., pp. 414– 420, 2005.
102. B.K. Chakravarthy, S. Gupta, S.S. Gambhir and K.D. Gode, “The prophylactic action of
(−) epicatechin against alloxan- induced diabetes in rats,” Life Sciences, vol. 29, pp. 2043-
2047, 1981.
103. M. Manickam, M. Ramanathan, M.A. Jahromi, J.P. Chansouria and A.B. Ray,
“Antihyperglycemic activity of phenolics from Pterocarpus marsupium ”, Journal of
Natural Products, vol. 60, pp. 609-610, 1997.
104. B.K. Chakravarthy, S. Gupta and K.D. Gode, “Functional Beta cell regeneratio n in the
islets of pancreas in alloxan induced diabetic rats by (-)-Epicatechin,” Life Sciences, vol.
31, pp. 2693-2697, 1982.
106. M.A. Jahromi and A.B. Ray,“Antihyperlipidemic effect of flavonoids from Pterocarpus
marsupium,” Journal of Natural Products, vol. 56, pp. 989–994, 1993.
107. F. Ahmad, P. Khalid, M.M. Khan, A.K. Rastogi and J.R. Kidwai, “Insulin like activity in
(-) epicatechin,” Acta Diabetologica Latina, vol. 26, pp. 291–300, 1989.
108. S.I. Rizvi and M.A. Zaid, “Intracellular reduced glutathione content in normal and type 2
diabetic erythrocytes: effect of insulin and (-)epicatechin,” Journal of Physiology and
Pharmacology vol. 52, no. 3, pp. 483-488, 2001.
25
109. I. Cordero-Herrera , M.A. Martín , L. Bravo , L. Goya and S. Ramos, “ Cocoa flavonoids
improve insulin signalling and modulate glucose production via AKT and AMPK in
HepG2 cells,” Molecular Nutrition and Food Research, 2013.
111. P. Kumar , R.K. Kale and N.Z. Baquer, “Antihyperglycemic and protective effects
of Trigonella foenum graecum seed powder on biochemical alterations in alloxan diabetic
rats,” European Reviews in Medicine and Pharmacology Sciences, vol. 16, no. 3, pp. 18-
27, 2012.
113. R.D. Sharma, T.C. Raghuram and N.S. Rao, “ Effect of fenugreek seeds on blood glucose
and serum lipids in type I diabetes,” European Journal of Clinical Nutrition, vol. 44, pp.
301–306, 1990.
114. A. Gupta, R. Gupta and B. Lal, “Effect of Trigonella foenum-graecum (fenugreek) seeds
on glycaemic control and insulin resistance in type 2 diabetes mellitus: A double blind
placebo controlled study,” Journal of Association of Physicians India, vol. 49, pp. 1057–
1061, 2001.
115. V. Vats, J.K Grover and S.S. Rathi, “ Evaluation of anti- hyperglycemic and
hypoglycemic effect of Trigonella foenum-graecum Linn, Ocimum sanctum Linn and
Pterocarpus marsupium Linn in normal and alloxanized diabetic rats,” Journal of
Ethnopharmacology vol. 79, pp. 95–100, 2002.
116. P.R. Petit, Y.D. Sauvaire, D.M. Hillaire-Buys, O.M. Leconte, Y.G. Baissac, G.R. Ponsin,
et al., “ Steroid saponins from fenugreek seeds extraction, purification, and
pharmacological investigation on feeding behavior and plasma cholesterol” Steroids, vol.
60, pp. 674–680, 1995.
26
117. Y. Sauvaire, P. Petit, C. Broca, M. Manteghetti, Y. Baissac, J.F. Alvarez, et al, “ 4-
Hydroxyisoleucine: A novel amino acid potentiator of insulin secretion,” Diabetes, vol.
47, pp. 206–210, 1998.
118. T.C. Raghuram, R.D. Sharma, B. Sivakumar and K. Sahay, “Effect of fenugreek seeds on
intravenous glucose disposition in non- insulin dependent diabetic patients,” Phytotherapy
Research, vol. 8, pp. 83–86, 1994.
119. L. Ali, A. Kalam, A. Khan, Z. Hassan, M. Mosihuzzaman, N. Nahar, et al.,
“ Characterization of the hypoglycemic effects of Trigonella foenum-graecum seed,”
Planta Med, vol. 61, pp. 358–360, 1995.
120. G. Ribes, Y. Sauvaire, C. Da Costa, J.C. Baccou, M.M and Loubatieres- Mariani,
“Antidiabetic effects of subfractions from fenugreek seeds in diabetic dogs,” Proceedings
Society Experimental Biology Medicine, vol. 182, pp. 159–166, 1986.
121. S. Genet, R.K. Kale and N.Z. Baquer, “Effects of vanadate, insulin and fenugreek
(Trigonella foenum graecum) on creatinine kinase levels in tissues of diabetic rat,” Indian
Journal of Experimental Biology, vol. 37, no. 2, pp. 200-202, 1999.
122. A.B Singh, A.K Tamarkar, T. Narender and A.K. Srivastava, “ Antihyperglycemic effect
of an unusual amino acid (4- hydroxyisoleucine) in C57BL/KsJ-db/db mice,” Natural
Product Research, vol. 24, pp. 258–265, 2010.
123. K. Hamden, B. Jaouadi, S. Carreau, A. Aouidet, S. El-Fazaa, N. Gharbi, et al., “ Potential
protective effect on key steroidogenesis and metabolic enzymes and sperm abnormalities
by fenugreek steroids in testis and epididymis of surviving diabetic rats,” Archives of
Physiology and Biochemistry, 2010; 116:146–155.
124. K. Hamden, H. Masmoudi, S. Carrea and A. Elfeki, “Immunomodulatory, β-cell, and
neuroprotective actions of fenugreek oil from alloxan- induced diabetes,”
Immunopharmacology Immunotoxicology, vol. 32, pp. 437–445, 2010.
125. G.S. Kumar , A.K. Shetty and P.V. Salimath, “Modulatory effect of fenugreek seed
mucilage and spent turmeric on intestinal and renal disaccharidases in streptozotocin
induced diabetic rats,” Plant Foods for Human Nutrition, vol. 60, no. 2, pp. 87-91, 2005.
126. Y. Sugihara, H. Nojima, H. Matsuda, T. Murakami, M. Yoshikawa and I. Kimura,
"Antihyperglycemic effects of gymnemic acid IV, a compound derived from Gymnema
27
sylvestre leaves in streptozotocin-diabetic mice," Journal of Asian Natural Products
research, vol. 2, no. 4, pp., 321–7, 2000.
127. H. Luo, L.F. Wang, T. Imoto and Y. Hiji, "Inhibitory effect and mechanism of acarbose
combined with gymnemic acid on maltose absorption in rat intestine," World Journal of
Gastroenterology, vol. 7, no. 1, pp. 9–15, 2001.
128. L.F. Wang, H. Luo, M. Miyoshi, T. Imoto, Y. Hiji and T. Sasaki, "Inhibitory effect of
gymnemic acid on intestinal absorption of oleic acid in rats". Canadian Journal of
Physiology and Pharmacology, vol. 76, no. 10–11, pp. 1017–23, 1998.
129. H. Asare-Anane, G.C. Huang, S.A. Amiel, P.M. Jones and S.J. Persaud, "Stimulation of
insulin secretion by an aqueous extract of Gymnema sylvestre: role of intracellular
calcium". Endocrine Abstracts 10: DP1, 2005.
130. S.J. Persaud, H. Al-Majed, A Raman and PM Jones "Gymnema sylvestre stimulates
insulin release in vitro by increased membrane permeability," Journal of Endocrinology,
vol. 163, no. 2, pp. 207–212, 1999.
131. S. Gholap and A. Kar, "Effects of Inula racemosa root and Gymnema sylvestre leaf
extracts in the regulation of corticosteroid induced diabetes mellitus: involvement of
thyroid hormones". Pharmazie, vol. 58, no. 6, pp. 413–415, 2003.
132. M.J. Leach, “Gymnema sylvestre for diabetes mellitus: a systematic review,” Journal of
Alternnative and Complementary Medicine,” vol. 13, no. 9, pp. 977-983, 2007.
133. H. Preuss, D. Bagchi and M. Bagchi, “Effects of a natural extract of (-)-hydroxycitric
acid (HCA-SX) and combination of HCA-SX plus niacin-bound chromium and
Gymnema sylvestre extract on weight loss,” Diabetes Obesity and Metabolism, vol. 6,
pp. 171, 2004.
134. W.T. Cefalu, J. Ye and Z.Q. Wang, “Efficacy of dietary supplementation with botanicals
on carbohydrate metabolism in humans,” Endocrine Metabolism and Immune Disorders
as Drug Targets, vol. 8, no. 2, pp.78-81, 2008.
135. A. Al- Romaiyan, B. Liu, H. Asare-Anane, C.R. Maity, S.K. Chatterjee, N. Koley, et al,
“ A novel Gymnema sylvestre extract stimulates insulin secretion from human islets in
vivo and in vitro,” Phytotherapy Research, vol. 24, no. 9, pp. 1370-1376, 2010.
28
induced diabetic albino male rats,” Asia Pacific Journal of Tropical Biomedicine, pp.
S930-S933, 2012.
137. B. Liu, H. Asare-Anane, A. Al- Romaiyan, G. Huang, S.A. Amiel, P.M. Jones, et al., “
Characterisation of the insulinotropic activity of an aqueous extract of Gymnema
sylvestre in mouse beta-cells and human islets of Langerhans,” Cell Physiology and
Biochemistry, vol. 23, no. 1- 3, pp. 125-32, 2009.
138. A.R. Saltiel and C.R. Kahn, “Insulin signaling and the regulation of glucose and lipid
metabolism,” Nature, vol. 414, pp. 799, 2001.
139. S.K. Jain, “Glutathione and glucose-6-phosphate dehydrogenase deficiency can increase
protein glycation,” Free Radical Biology Medicine, vol. 24, no. 1, pp. 197, 1998.
140. E. Block, “The chemistry of garlic and onions,” Scenitific American, vol. 252, pp. 114-
119, 1985.
141. M. Ali, M. Thomson and M. Afzal, “Garlic and onions: their effect on eicosanoid
metabolism and its clinical relevance,” Prostaglandins and Leukotrine Essentials, vol.
62, no. 2, pp. 55-73, 2000.
142. K. P. Pathirage and Li Yunman, “Functional herbal food ingredients used in type 2
diabetes mellitus,” Pharmacognosy Reviews, vol. 6, no. 11, pp. 37–45, 2012.
143. K.T Augusti and P.T. Mathew, “Lipid lowering effect of allicin (diallyl disulfide oxide)
on long-term feeding in normal rats,” Experientia, vol. 30, pp. 468-470, 1974.
144. P. Rose, M. Whiteman, P.K. Moore and Y.Z. Zhu, “Bioactive Salk (en) yl cysteine
sulfoxide metabolites in the genus Allium: the chemistry of potential therapeutic agents,”
Natural Product Reports, vol. 22, pp. 351-368, 2005.
146. C.T. Liu, H. Hse, C.K. Lii, P.S. Chen and L.Y. Sheen, “Effects of garlic oil and diallyl
trisulfide on glycemic control in diabetic rats,” European Journal of Pharmacology, vol.
516, pp. 165–73, 2005.
147. P.T. Mathew and K.T. Augusti, “Studies on the effect of allicin (diallyl disulphide-oxide)
on alloxan diabetes I. Hypoglycaemic action and enhancement of serum insulin effect
and glycogen synthesis,” Indian Journal Biochemistry and Biophysics, vol. 10, pp. 209–
12, 1973.
29
148. R.C. Jain and C.R. Vyas, “Hypoglycemic action of onion and garlic,” American Journal
of Clinical Nutrition,” vol 28, pp. 684–5, 1975.
149. S.Yeda Diniz, K.H.R. Rocha Katiucha , A. Souza Gisele , M. Galhardi Cristiano, M.X.
Ebaid Geovana, G. Rodrigues Hosana , V.B. Novelli Filho José Luiz, C. Cicogna
Antonio and L.B. Novelli Ethel, “ Effects of N-acetylcysteine on sucrose-rich diet-
induced hyperglycaemia,dyslipidemia and oxidative stress in rats,” European Journal of
Pharmacology, vol. 543, pp. 151–157, 2006.
150. B.O. Bever and G.R. Zahnd, “Plants with oral hypoglycemic action,” Q Journal Crude
Drug Research, vol. 17, pp. 139–149, 1979.
151. F.M. Al-awadi and K.A. Gumaa, “Studies on the activity of individual plants of an
antidiabetic plant mixture,” Acta Diabetologica Latina, vol. 24, pp. 37–41, 1987.
152. K.T. Augusti and C.G. Shella, “Antiperoxide effect of S-allyl cysteine sulfoxide, an
insulin secretagogue in diabetic rats,” Experientia, vol. 52, pp. 115–120, 1996.
155. F.M. El-Demerdash, M.I. Yousef and N.I. Abou El-Naga, “Biochemical study on the
hypoglycemic effects of onion and garlic in alloxan- induced diabetic rats,” Food and
Chemical Toxicology,” vol. 43, pp. 57–63, 2005.
156. C. Borek, “Antioxidant health effects of age garlic extract,” Journal of Nutrition, vol.
131, pp. 1010S-1015S, 2001.
157. J.Z. Liu, X.Y. Lin and J.A. Milner, “Dietary garlic powder increases glutathione content
and glutathione S-transferase activity in rat liver and mammary tissues,” FASEB J, vol.,
6: A3230 (abstract), 1992.
158. H.R. Madkor , S.W. Mansour and G. Ramadan , “ Modulatory effects of garlic, ginger,
turmeric and their mixture on hyperglycaemia, dyslipidaemia and oxidative stress in
streptozotocin- nicotinamide diabetic rats,” British Journal of Nutrition, vol. 105, no. 8,
pp. 1210-1217, 2011.
159. R. Padiya , T.N. Khatua , P.K. Bagul , M. Kuncha and S.K. Banerjee, “ Garlic improves
insulin sensitivity and associated metabolic syndromes in fructose fed rats,” Nutrition and
Metabolism (Lond) , vol. 8, pp. 53, 2011.
30
160. M.S. Ahmad and N. Ahmed, “Antiglycation properties of aged garlic extract: Possible
role in prevention of diabetic complications,” Journal of Nutrition, vol. 136, no. Suppl 3,
pp. 796S–799S, 2006.
31