EFFECT OF GARLIC (ALLIUM SATIVUM L) ON BIOCHEMICAL PARAMETERS AND HISTOPATHOLOGY OF PANCREAS OF ALLOXAN-INDUCED DIABETIC RATS

Authors

  • Lilia Douaouya Department of Cellular and Molecular Biology, Faculty of Sciences, Khenchela University, Khenchela, 40004, Algeria
  • Noureddine Bouzerna

Keywords:

(Garlic, Diabetes, Biochemical parameters, Glibenclamide, Pancreas, Rat)

Abstract

Objective: Garlic (Allium sativum. L) plays an important dietary role, as well as medicinal, for centuries. Even today the use of garlic is widespread and growing. The present study investigated the effect of garlic extract and glibenclamide on biochemical parameters, enzyme activities, and reduced glutathione (GSH) content in the liver as well as on pancreas tissue in alloxan-induced diabetic rats.

Methods: Diabetes mellitus was induced in 28 out of 35 adult male albino rats, using an intraperitoneal injection of 150 mg/kg body weight of alloxan. The diabetic rats were divided into four groups, two of which were administered orally by garlic extract (250 and 500 mg/kg) and a group composed of diabetic rats was given the standard drug, glibenclamide, orally at a dose of 2.5 mg/kg. The control rats (normal and diabetic) were fed normal saline, once daily for 21 d.

Results: Oral administration of the garlic extract significantly decreased blood glycosylated hemoglobin, serum glucose, total cholesterol, triglycerides, total lipids, glutamic oxalic transaminase (GOT), glutamic pyruvic transaminase (GPT), lactate dehydrogenase (LDH), and alkaline phosphatase (ALP) levels, with significant increase in plasma insulin, and GSH content in liver of alloxan-diabetic rats in dose–dependent fashion which was comparable to an antidiabetic standard drug, glibenclamide, given at a dose of 2.5 mg/kg. Concurrent histological studies of the pancreas of these animals have confirmed the changes observed in biochemical parameters and proved the comparable preventive effect of garlic extract.

Conclusion: These results suggest the potential of garlic extract as a histo protective against free-radical-associated diabetes damage, preserving the ability of insulin secretion, and show a concentration-dependent antidiabetic effect.

Keywords: Garlic, Diabetes, Biochemical parameters, Glibenclamide, Pancreas, Rat

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References

Chandra A, Singh RK, Tewari L. Antioxidative potential of herbal hypoglycemic agents in diabetes—an overview. SFRR. Indian Bull 2004;3:24–6.

Kesari AN, Kesari S, Singh SK, Gupta RK, Watal G. Studies on the glycemic and lipidemic effect of Murraya koenigii in experimental animals. J Ethnopharmacol 2007;112:305–11.

Day C. Traditional plant treatment for diabetes mellitus: pharmaceutical foods. Britain J Nutr 1998;80:5–6.

Elkayam A, Mirelman D, Peleg E. The effects of allicin on weight in fructose-induced hyperinsulinemic, hyperlipidemic, hypertensive rats. Am J Hypertension 2003;16:1053–6.

Thomson M, Al-Qattan KK, Bordia T, Muslim A. Supplement: significance of garlic and its constituents in cancer and cardiovascular disease. Including garlic in the diet may help lower blood glucose, cholesterol, and triglycerides. J Nutr 2006;136:800-2.

Salman H, Bergman M, Bessler H, Punsky I, Djaldetti M. Effect of a garlic derivative (alliin) on peripheral blood cell immune responses. Int J Immunopharmacol 1999;21:589-97.

Wang BH, Zuzel KA, Rahman K, Billington D. Treatment with aged garlic extract protects against bromobenzene toxicity to precision-cut rat liver slices. Toxicology 1999;132:215-25.

Chung LY. The antioxidant properties of garlic compounds: allyl cysteine, alliin, allicin, and allyl disulfide. J Med Food 2006;9:205–13.

Newall CA, Anderson LA, Phillipson JD. Herbal medicines: a guide for health-care professionals. London: Pharmaceutical Press; 1996. p. 296.

Fröde TS, Medeiros YS. Animal models to test drugs with pote ntial antidiabetic activity. J Ethnopharmacol 2008;115:173-83.

Anderson L, Dinesen B, Jorgensen PN, Poulsen F, Roder MF. Enzyme immunoassay for intact human insulin in serum or plasma. Clin Chem 1996;38:578.

Kaplan LA, Rubaltelli FF, Hammerman C, Vilei MT, Leiter C, Abramov A. Lipids. In: Kaplan LA, Pesce AJ. Eds. Clin Chem: Theory, Analysis and Correlatio n. St Louis. Toronto. Princeton: The C. V. Mosby Company; 1984. p. 918-9.

Trinder P. Enzymatic colorimetric method for cholesterol measurements. Ann Clin Biochem 1969;6:24.

Buccoolo G. Quantitative determination of serum triglcerides by use of enzymes. Clin Chem 1973;19:476.

Bisse E, Abraham EC. New less temperature sensitive micro chromatographic method for the separation and quantization of glycosylated haemoglobin using a noncyanide buffer system. J Chromatog 1985;344:81-91.

Bergmeyer H, Walefeld M. Méthode cinétique pour la détermination du TGO et TGP sans phosphate de pyridoxal. Clin Chem Acta 1978;24:58.

Pesce A. Lactate dehydrogenase. Kaplan A. Clin Chem the C. V 1984;1117:24, 438.

Bowers GNJ, Mc Comb RB. A continuous spectrophotometric method for measurement the activity of serum alkaline phosphatase. Clin Chem 1966;12-73.

Bradford M. A rapid and sensitive method for the quantities of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976;72:248–54.

Weakberker G, Cory JC. Ribonucleotide reductase activity and growth of glutathione-depended mouse leukaemia L1210 cells in vitro. Cancer Lett 1988;40:257-64.

Houlot R. Techniques d’histopathologie et de cytopathologie. Ed Maloine; 1984. p. 225-7.

Hincu M, Pantea S, Anca M, Coman EM, Mehedinti T. L’effet de l’alloxane sur l’histologie du tissu pancréatique. Fascicula XVII, Anul V; 2006.

Vats V, Yadav SP, Grover JK. Ethanolic extract of Ocimum sanctum leaves partially attenuates streptozotocin induced alterations in glycogen content and carbohydrate metabolism in rats. J Ethnopharmacol 2004;90:155–60.

Chang MLW, Johnson MA. Effect of garlic on carbohydrate metabolism and lipid synthesis in rats. J Nutr 1980;110:931–6.

El-Tantawy WH, Soliman ND, El-naggar D, Shafei A. Investigation of antidiabetic action of Antidesma bunius extract in type 1 diabetes. Arch Physiol Biochem 2015;121:116-22.

Augusti KT. Therapeutic values of onion (Allium cepa) and Garlic (Allium sativum). Indian J Exp Biol 1996;34:634–40.

Joshi DV, Patil RR, Naik SR. Hydroalcohol extract of Trigonella foenum-graecum seed attenuates markers of inflammation and oxidative stress while improving exocrine function in diabetic rats. Pharm Biol 2015;53:201-11.

Yates AP, Laing I. Age-related increase in haemoglobin A1c and fasting plasma glucose is accompanied by a decrease in beta cell function without a change in insulin sensitivity: evidence from a cross-sectional study of hospital personnel. Diabetic Med 2002;19:254-8.

Shirwaikar A, Rajendran K, Kumar CD, Bodla R. Antidiabetic activity of aqueous leaf extract of Annona squamosa in streptozotocin-nicotinamide type 2 diabetic rats. J Ethnopharmacol 2004;91:171–5.

Knipschild JK, Ter-Riet G. Garlic, onions and cardiovascular risk factors. A review of the evidence from human experiments. Emphasis on commercially available preparations. Br J Clin Pharmacol 1989;28:535–44.

Gebhardt R, Beck H. Differential inhibitory effects of garlic-derived organosulfur compounds on cholesterol biosynthesis in primary rat hepatocyte cultures. Lipids 1996;31:1269–76.

Balasenthil S, Arivazhagan S, Nagini S. Garlic enhances circulatory antioxidants during 7, 12-dimethylbenz anthracene-induced hamster buccal pouch carcinogenesis. J Ethnopharmacol 2000;72:429–33.

Hultcrantz R, Glaumann H, Lindberg G. Liver investigation in 149 asymptomatic patients with moderately elevated activities of serum aminotransferases. Scand J Gastroenterol 1986;21:109–13.

Navarro CM, Montilla PM, Martin A, Jimenez J, Utrilla PM. Free radicals scavenger and antihepatotoxic activity of Rosmarinus. Plant Med 1993;59:312-4.

Eidi A, Eidi M, Esmaelli E. Antidiabetic effect of garlic (Allium sativum) in normal and streptozotocin-induced diabetic rats. Phytomedicine 2006;13:624–9.

Bhattacharya S, Gachhui R, Sil PC. Effect of Kombucha, a fermented black tea in attenuating oxidative stress mediated tissue damage in alloxan induced diabetic rats. Food Chem Toxicol 2013;60:328-40.

Inove M, Saito Y, Hirato E, Morino Y, Nagase S. Regulation of redox status of plasma proteins by metabolism and transport of glutathione and related compounds. J Protein Chem 1987;36:169–73.

Kumkrai P, Kamonwannasit S, Chudapongse N. Cytoprotective and anti-diabetic effects of Derris reticulata aqueous extract. J Physiol Biochem 2014;70:675-84.

El-far M, Negm A, Abd El-azim A, Wahdan M. Antioxidant therapeutic actions of medicinal phytochemicals, silymarin and silibinin, on streptozotocin diabetic rats: first novel comparative assessment of structural recoveries of histological and ultrastructural changes on islets of langerhans, β-cells, mitochondria and nucleus. Int J Pharm Pharm Sci 2016;8:69-76.

Banerjee SK, Dinda AK, Manchanda SC, Maulik SK. Chronic garlic administration protects heart against oxidative stress induced by ischemic reperfusion injury. BMC Phamacol 2002;2:2-16.

Published

01-06-2016

How to Cite

Douaouya, L., and N. Bouzerna. “EFFECT OF GARLIC (ALLIUM SATIVUM L) ON BIOCHEMICAL PARAMETERS AND HISTOPATHOLOGY OF PANCREAS OF ALLOXAN-INDUCED DIABETIC RATS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 8, no. 6, June 2016, pp. 202-6, https://journals.innovareacademics.in/index.php/ijpps/article/view/11378.

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