HYPOGLYCEMIC AND HYPOLIPIDEMIC EFFECTS OF PHENOLIC OLIVE TREE EXTRACT IN STREPTOZOTOCIN DIABETIC RATS

Authors

  • Wafa Laaboudi Biotechnology Laboratory, Faculty of Science Dhar El Mahraz, University Sidi Mohamed Ben Abdellah - Fez - Morocco
  • Jamal Ghanam Biotechnology Laboratory, Faculty of Science Dhar El Mahraz, University Sidi Mohamed Ben Abdellah - Fez - Morocco
  • Oumaima Ghoumari Biotechnology Laboratory, Faculty of Science Dhar El Mahraz, University Sidi Mohamed Ben Abdellah - Fez - Morocco
  • Fatiha Sounni Biotechnology Laboratory, Faculty of Science Dhar El Mahraz, University Sidi Mohamed Ben Abdellah - Fez - Morocco
  • Mohammed Merzouki Biotechnology Laboratory, Faculty of Science Dhar El Mahraz, University Sidi Mohamed Ben Abdellah - Fez - Morocco
  • Mohamed Benlemlih Biotechnology Laboratory, Faculty of Science Dhar El Mahraz, University Sidi Mohamed Ben Abdellah - Fez - Morocco

DOI:

https://doi.org/10.22159/ijpps.2016v8i12.14077

Keywords:

Olive leaves, Olive fruit, Polyphenols, Antidiabetic, Streptozotocin, In vivo

Abstract

Objective: The aim of the present study was to determine the effects of an olive tree extract with high polyphenols content on blood glucose level and other related parameters in streptozotocin-induced diabetic rats.

Methods: Diabetes was induced in rats by intraperitoneal injection of streptozotocin (55 mg/kg bw). 72h after injection, rats with fasting blood glucose higher than 2 g/l were used for the experiments. Olive tree extract was administered for 28 d and blood glucose level was measured every 4 d. Total cholesterol, triglycerides, HDL-cholesterol, creatinine, urea, total protein, uric acid, aspartate aminotransferase and alanine aminotransferase levels, were determined at the end of the experiment.

Results: The oral administration of olive tree extract contributes to blood glucose level decreasing in diabetic rats group, which was significantly lower at 4th week compared to the diabetic control rats. Moreover, supplementation by olive tree extract decreased significantly (p<0.05) the values of total cholesterol, triglycerides, HDL-cholesterol, creatinine, urea, total protein, uric acid, aspartate aminotransferase and alanine aminotransferase resulting from damage caused by streptozotocin treatment. Beside this, significant reduce (p<0.05) in heart disease risk ratio was observed for treated group (4.1±0.14) compared to untreated group (7.64±0.36), which was quite similar to normal rats (4.50±0.36). Studied olive tree extract effects were similar to those of glibenclamide, a well-known antidiabetic drug.

Conclusion: Results herein obtained reveal the hypoglycemic effect of this olive tree extract, suggesting his potential use as a natural antidiabetic agent.

Downloads

Download data is not yet available.

References

Gonzalez M, Zarzuelo A, Gamez MJ, Utrilla MP, Jimenez J, Osuna I. Hypoglycemic activity of olive leaf. Planta Med 1992;58:513-5.

Oberley LW. Free radicals and diabetes. J Biol Chem 1988;5:113-24.

Jennings PE, McLaren M, Scot NA, Saniabadi AR, Belch JJF. The relationship of oxidative stress to the thrombotic tendency in type I diabetic patients with retinopathy. Diabetic Med 1991;8:860-5.

Lyons TJ. Oxidized low-density lipoproteins: a role in the pathogenesis of atherosclerosis in diabetes? Diabetic Med 1999;8:411-9.

Valezquez E, Wincour PH, Kestsven P, Alberti KGMM, Laker MF. Relation of lipid peroxides to macrovascular disease in type 2 diabetes. Diabetic Med 1991;8:752-8.

Duckworth WC. Hyperglycemia and cardiovascular disease. Curr Atheroscler 2001;3:383-91.

Thripathi BK, Sivastava AK. Diabetes mellitus: complication and therapeutic. Med Sci Monit 2006;12:130-47.

Holman RR, Turner RC. Oral agents and insulin in the treatment of NIDDM. In: Textbook of Diabetes. Pickup J, Williams G. eds. Blackwell: Oxford; 1991.

Rupeshkumar M, Kavitha K, Haldar PK. The role of herbal plants in the diabetes mellitus therapy: an overview. Int J Appl Pharm 2014;6:1-3.

De Marco E, Savarese M, Paduano A, Sacchi R. Characterization and fractionation of phenolic compounds extracted from olive oil mill wastewaters. Food Chem 2007;104:858-67.

Richard N, Arnold S, Hoeller U, Kilpert C, Wertz K, Schwager J. Hydroxytyrosol is the major anti-inflammatory compound in aqueous olive extracts and impairs cytokine and chemokine production in macrophages. Planta Med 2011;77:1890-7.

Fortes C, García-Vilas J, Quesada A, Medina M. Evaluation of the anti-angiogenic potential of hydroxytyrosol and tyrosol, two bioactive phenolic compounds of extra virgin olive oil, in endothelial cell cultures. Food Chem 2012;134:134-40.

Briante R, Patumi M, Terenziani S, Bismuto E, Febbraio F, Nucci R. Olea europaea L. leaf extract and derivatives: antioxidant properties. J Agric Food Chem 2002;17:4934-40.

Fitó M, Cladellas M, Torre R, Martí J, Muñoz D, Schröder H. Anti-inflammatory effect of virgin olive oil in stable coronary disease patients: a randomized, crossover, controlled trial. Eur J Clin Nutr 2007;62:570-4.

Covas MI, Nyyssonen K, Poulsen HE, Kaikkonen J, Zunft HJ, Kiesewetter H. The effect of polyphenols in olive oil on heart disease risk factors: a randomized trial. Ann Intern Med 2006;145:333-41.

Rahman I, Biswas SK, Kirkham PA. Regulation of inflammation and redox signaling by dietary polyphenols. Biochem Pharmacol 2006;72:1439-52.

Brunelleschi S, Bardelli C, Amoruso A, Gunella G, Ieri F, Romani A, et al. Minor polar compounds extra-virgin olive oil extract (Mpc-Ooe) inhibits Nf-Kb translocation in human Monocyte/Macrophages. Pharmacol Res 2007;56:542-9.

Pacheco YM, Bermudez B, Lopez S, Abia R, Villar J, Muriana FJG. Minor compounds of olive oil have postprandial anti-inflammatory effects. Br J Nutr 2007;98:260-3.

Laaboudi W, Ghanam J, Aissam H, Merzouki M, Benlemlih M. Anti-inflammatory and analgesic activities of olive tree extract. Int J Pharm Pharm Sci 2016;8:414-9.

Ghanam J, Laaboudi W, Benlemlih M. Effects of rich polyphenols olive tree extract on inflammation and pain in patients with rheumatoid arthritis: an 8-weeks randomized, double-blind, placebo-controlled clinical trial. Int J Biol Pharm Res 2015;2:51-61.

Fabiani R, De Bartolomeo A, Rosignoli P, Servili M, Montedoro G, Morozzi G. Cancer chemoprevention by hydroxytyrosol isolated from virgin olive oil through G1 cell cycle arrest and apoptosis. ‎Eur J Cancer Prev 2002;11:351-38.

Bouallagui Z, Han J, Isoda H, Sayadi S. Hydroxytyrosol rich extract from olive leaves modulates cell cycle progression in Mcf-7 human breast cancer cells. Food Chem Toxicol 2011;49:179-84.

Hamden K, Allouche N, Damak M, Elfeki A. Hypoglycemic and antioxidant effects of phenolic extracts and purified hydroxytyrosol from olive mill waste in vitro and in rats. ‎Chem Biol Interact 2009;180:421-32.

Wainstein J, Ganz T, Boaz M, Bar-Dayan Y, Dolev E, Kerem Z, et al. Olive leaf extract as a hypoglycemic agent in both diabetic human subjects and in rats. J Med Food 2012;15:605-10.

Eidi A, Eidi M, Darzi R. Antidiabetic effect of Olea europaea L. in normal and diabetic rats. ‎Phytother Res 2009;23:347-50.

Mousa HM, Farahna M, Ismail MS, Al-Hassan AA, Ammar AS, Abdel-Salam AM. Anti-diabetic effect of olive leaves extracts in alloxan-diabetic rats. J Agric Vet Sci 2014;7:183-92.

Karaosmanoglu H, Soyer F, Ozen B, Tokatli F. Antimicrobial and antioxidant activities of Turkish extra virgin olive oils. J Agric Food Chem 2010;58:8238-45.

Zhao G, Yin Z, Dong J. Antiviral efficacy against hepatitis b virus replication of oleuropein isolated from Jasminum Officinale L. Var. Grandiflorum. J Ethnopharmacol 2009;125:265-8.

Battinelli L, Daniele C, Cristiani M, Bisignano G, Saija A, Mazzanti G. In vitro antifungal and anti-elastase activity of some aliphatic aldehydes from Olea europaea L. fruit. Phytomedicine 2006; 13:558-63.

Medina E, De Castro A, Romero C, Brenes M. Comparison of the concentrations of phenolic compounds in olive oils and other plant oils: correlation with antimicrobial activity. J Agric Food Chem 2006;54:4954-61.

Visioli F, Poli A, Galli C. Antioxidant and other biological activities of phenols from olives and olive oil. Med Res Rev 2002;22:65-75.

Manna C, Della Ragione F, Cucciola V, Borriello A, D’Angelo S, Galletti P, et al. Biological effects of hydroxytyrosol, a polyphenol from olive oil endowed with antioxidant activity. Adv Exp Med Biol 1999;472:115-30.

Yamada K, Ogawa H, Hara A, Yoshida Y, Yonezawa Y, Karibe K, et al. Mechanism of the antiviral effect of hydroxytyrosol on influenza virus appears to involve a morphological change of the virus. Antiviral Res 2009;83:35-44.

Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. ‎Clin Chem 1972;18:499-502.

Lemieux I, Lamarche B, Couillard C, Pascot A, Cantin B, Bergeron J, et al. Total cholesterol/HDL cholesterol ratio vs LDL cholesterol/HDL cholesterol ratio as indices of ischemic heart disease risk in men: the quebec cardiovascular study. Arch Med Res 2001;161:2685-92.

Rakieten N, Rakieten ML, Nadkarni MV. Studies on the diabetogenic action of streptozotocin (NSC-37917). Cancer Chemother Rep 1963;29:91-8.

Lenzen S., The mechanisms of alloxan and streptozotocin, induced diabetes. Diabetologia 2008;51:216-26.

Reed MJ, Meszaros K, Entes LJ, Claypool MD, Pinkett JG, Gadbois TM, et al. A new rat model of type 2 diabetes: the fat-fed, streptozotocin-treated rat. Metabolism 2000;49:1390-4.

Srinivasan K, Viswanad B, Asrat L, Kaul CL, Ramarao P. Combination of high-fat-diet-fed and low-dose streptozotocin-treated rat: a model for type 2 diabetes and pharmacological screening. Pharmacol Res 2005;52:313-20.

Szkudelski T. The mechanism of alloxan and streptozotocin action in B cells of the rat pancreas. Physiol Res 2001;50:537-46.

Putta S, Chedalawada V. Dose-dependent effect on hypoglycemic and antihyperglycemic activities of the chloroform extract of physalis minima in streptozotocin-induced diabetic rats. Int J Curr Pharm Res 2014;6:61-5.

Laaboudi W, Ghanam J, Merzouki M, Benlemlih M. Eco-extraction of phenolic compounds from Moroccan olive fruits and leaves and their potential use as antimicrobial agents. Eur J Sci Res 2015;132:255-65.

Silvestre RA, Egido EM, Hernandez R, Marco J. Tungstate stimulates insulin release and inhibits somatostatin output in the perfused rat pancreas. Eur J Pharmacol 2005;519:127-34.

Nivitabishekam SN, Asad M, Prasad VS. Pharmacodynamic interaction of Momordica charantia with rosiglitazone in rats. Chem Biol Interact 2009;177:247-53.

Rhoads GG, Gulbrandsne CL, Kagan A. Serum lipoproteins and coronary heart disease in a population study of Hawaii Japanese men. New Engl J Med 1976;294:293-8.

Camargo A, Rangel-Zuñiga OA, Haro C, Meza-Miranda ER, Peña-Orihuela P, Meneses ME, et al. Olive oil phenolic compounds decrease the postprandial inflammatory response by reducing postprandial plasma lipopolysaccharide levels. Food Chem 2014;162:161-71.

Hu FB. The Mediterranean diet and mortality-olive oil and beyond. New Engl J Med 2003;348:2595-6.

Estruch R, Martinez-Gonzalez MA, Corella D, Salas-Salvadó J, Ruiz-Gutiérrez V, Covas MI. Effects of a mediterranean-style diet on cardiovascular risk factors: a randomized trial. Ann Intern Med 2006;145:1-11.

Scoditti E, Calabriso N, Massaro M, Pellegrino M, Storelli C, Martines G. Mediterranean diet polyphenols reduce inflammatory angiogenesis through MMP-9 and COX-2 inhibition in human vascular endothelial cells: a potentially protective mechanism in atherosclerotic vascular disease and cancer. Arch Biochem Biophys 2012;527:81-9.

Madianov IV, Balabolkin MI, Markov DS, Markova TN. Main causes of hyperuricemia in diabetes mellitus. Ter Arkh 1999;72:55-8.

Almadal TP, Vilstrup H. Strict insulin treatment normalizes the organic nitrogen contents and the capacity of urea-N synthesis in experimental diabetes in rats. Diabetologica 1988;3:114-8.

Pratt DS, Kaplan MM. Evaluation of abnormal liver-enzyme results in asymptomatic patients. New Engl J Med 2000;342:1266-71.

Davie SJ, Gould BJ, Yudkin JS. Effect of vitamin C on glycosylation of proteins. Diabetes 1992;41:167-73.

Sinclair AJ, Girling AJ, Gray L, Lunec J, Barnett AH. An investigation of the relationship between free radical activity and vitamin C metabolism in elderly diabetic subjects with retinopathy. Gerontology 1992;38:268-74.

Lean ME, Noroozi M, Kelly I, Burns J, Talwar D, Sattar N, et al. Dietary flavonols protect diabetic human lymphocytes against oxidative damage to DNA. Diabetes 1999;48:176-81.

Mercuri F, Quagliaro L, Ceriello A. Review paper: oxidative stress evaluation in diabetes. Diabetes Technol Ther 2000;2:589-600.

Published

01-12-2016

How to Cite

Laaboudi, W., J. Ghanam, O. Ghoumari, F. Sounni, M. Merzouki, and M. Benlemlih. “HYPOGLYCEMIC AND HYPOLIPIDEMIC EFFECTS OF PHENOLIC OLIVE TREE EXTRACT IN STREPTOZOTOCIN DIABETIC RATS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 8, no. 12, Dec. 2016, pp. 287-91, doi:10.22159/ijpps.2016v8i12.14077.

Issue

Section

Original Article(s)

Most read articles by the same author(s)