Modulatory effect of an isolated compound from Syzygium cumini seeds on biochemical parameters of diabetes in rats
DOI:
https://doi.org/10.22377/ijgp.v3i2.428Abstract
In the search of natural hypoglycemic agents as alternatives to synthetic ones and to justify the use of Syzygium cumini seeds infolklore system of medicine for diabetes the present study was carried out. To evaluate the hypoglycemic and antioxidant activity of an isolated compound from S. cumini seeds in normal and non-insulin dependent diabetes mellitus (NIDDM) rats. Study was carried out in Wistar rats. Diabetes was induced by streptozotocin in neonates. Oral administration of petroleum ether, chloroform, acetone,methanol, and water extracts of S. cumini (100 mg/kg, p.o.) for 21 days caused a decrease in fasting blood sugar (FBS) in diabetic rats. Among all the extracts, methanol extract was found to lower the FBS significantly in diabetic rats. Glibenclamide was used as standard antidiabetic drug (5 mg/kg, p.o). Methanol extract was subjected to column chromatography that led to isolation of an active principle, which was given trivial name Cuminoside. Cuminoside (50 mg/kg, p.o.) was studied for its hypoglycemic and antioxidant
potential. The unpaired t-test and analysis of variance (ANOVA) followed by post hoc test were used for statistical analysis. Cuminoside caused a significant decrease in FBS level, lipidperoxidation level, and improvement in the levels of antioxidant enzymes (reduced glutathione, superoxide dismutase, and catalase) in diabetic rats. A considerable decrease in lipid peroxidation and improvement
in the antioxidant enzymes level in NIDDM rats indicated that Cuminoside has antioxidant potential with antidiabetic activity and provides a scientific rationale for the use of Cuminoside as an antidiabetic agent.
Key words: Antioxidants, β sitosterol, diabetes, lipid peroxidation, streptozotocin, Syzygium cumini
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References
Rajasekaran S, Ravi K, Sivagnanam K, Subramanian S. Beneficial
effect of aloe vera leaf gel extract on lipid profile status in rats with
streptozotocin diabetes. Clin Exp Pharmacol Physiol 2006;33:232-7.
Srinivasan K, Viswanad B, Asrat L, Kaul CL, Ramarao P.
Combination of high fat diet fed and low dose streptozotocin
treated rats: A model for type II diabetes and pharmacological
screening. Pharmacol Res 2005;52:313-20.
Saltiel AR, Olefsky JM. Thiazolidinediones in the treatment of
insulin resistance and type II diabetes. Diabetes 1996;45:1661-9.
Banerji MA, Lebovitz HE. Treatment of insulin resistance in
diabetes mellitus. Eurr J pharmacol 2001;490:135-46.
Amosa F, Carthy MC, Jimmet. The rising global burden of diabetes
and its complication: Estimation and protective to the year 2010.
Diabet Med 1998;14:51-85.
Deray G, Jacobs D. Radiocontrast nephrotoxicity: A review. Invest
Radiol 1995;30:221-5.
Baynes JW. Role of oxidative stress in the development of
complications in diabetes. Diabetes 1991;40:405-12.
Brown DJ, Goodman J. A review of Vitamin A, C, E and their
relationship to cardiovascular diaeases. Clin Excell Nurse Pract
;2:10-22.
Al-Awaidi FM, Khattar MA, Gumaa KA. ON the mechanism of the
hypoglycemic effect of a plant extract. Diabetologia 1985;18:432-4.
M Rakesh, V Wazir, R Kapil. Biotheraupatic diterpene glucoside
from tinospora cordifolia. J Indian Chem Sco 1995: 361.
Pushparaj P, Tan CH, Tan BK. Effects of Averrhoa bilimbi leaf
extract on blood glucose and lipids in streptozotocin-diabetic rats.
J ethanopharmacol 2000;72;69-76.
Kirtikar KR, Basu BD. In Indian Medicinal Plants. Vol. 2. New
Delhi: Periodical Experts; 1975. p. 1052-53.
Brahmachari HD, Augusti KT. Hypoglycemic agents from Indian
Indigenous plants. Journal of Pharmacy and Pharmacology 1961;
XIII (1): 1961,143.
Kar A, Choudhary BK, Bandyopadhyay NG. Comparative
evaluation of hypoglycaemic activity of some Indian medicinal
plants in alloxon diabetic rats. J Ethnopharmacol 2003;84:105-8.
Pepato MT, Mori DM, Baviera AM,. Harami JB, Vendramini RC,
Brunetti LL. Fruit of the jambolan tree (Eugenia jambolana Lam.) and
experimental diabetes. Journal of Ethnopharmacol 2002;96:43-8.
Sofowora A. Medicinal plants and traditional medicines in Africa.,
Chichester: John Wiley and Sons; 2003. p. 256-57.
Wall ME, Eddy CR, McClenna ML, Klump ME. Detection and
estimation of steroids and saponins in plant tissue. Anal Chem
:24:337-1342.
Ghosh MN. Fundamentals of experimental pharmacology. Kolkata:
Published by Hilton and Company; 2005. p. 190-7.
Portha B, Blondel O, Serradas P, McEvoy R, Giroix MH, Kergoat M,
et al. The rat models of non-insulin dependent diabetes induced
by neonatal streptozotocin. Diabete Metab 1989;15:61-75.
Sharma SR, Dweidi SK, Swarup D. Hypoglycemic,
antihyperglycemic and hypolipidemic activities of Caesalpinia
bonducella seeds in rats. J. Ethanopharmacol 1997:39-44.
Slater TF, Sawyer BC. The stimulatory effect of carbon tetrachloride
and other halogenalkane or peroxidative reaction in the rat liver
fraction in vitro. Biochem J 1971;12:805-14.
Moron MS, Depierre JW. Levels of glutathione, glutathione
reductase and glutathione S transferase activities in rat lung and
liver. Biochim Biophys Acta 1979;582:67-78.
Mishra, fridovich. The role of superoxide anion in the
autooxidation of epinephrine and a simple assay of SOD.J Biolchem
;243:3170- 5.
Cho SY, Park JY, Park EM, Choi MS, Lee MK, Jeon SM, Alteration
of hepatic antioxidant enzyme activities and lipid profile in
streptozotocin induced diabetic rats by supplementation of
dandelion water extract. Clin Chim Acta 2002;317:109-17.
Achrekar GS, Kaklij MS, Pote MS, Kelkar SM. Hypoglycemic
activity of Eugenia jambolana and Ficus bengalensis: Mechanism
of action. In Vivo 1991;5:143-7.