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Effects of three medicinal plants extracts in experimental diabetes: antioxidant enzymes activities and plasma lipids profiles in comparison with metformin
IJPR-Iranian Journal of Pharmaceutical Research. 2012; 11 (3): 897-903
Dans Anglais | IMEMR | ID: emr-160878
ABSTRACT
In the present study we aimed to evaluate the effects of methanolic extracts of the bulbs of Garlic [Allium sativum L., Alliaceae] and Persian shallot [Allium ascalonicum L., Alliaceae]and leaves of Sage [Salvia officinalis L., Lamiaceae], ASE, AAE and SOE respectively, on the antioxidant enzymes such as superoxide dismutase [SOD], glutathione peroxidase [GPX] and catalase [CAT] activities and on the levels of plasma lipids profiles such as triglycerides [TG], total cholesterol [TC], high-density lipoproteins [HDL], low-density lipoproteins [LDL] and very low-density lipoproteins [VLDL] in Alloxan diabetic Wistar rats. In comparison with diabetic control rats in diabetic treated rats, AAE increases the activities of SOD [65%], GPX [43%] and CAT [55%]. ASE and SOE increase SOD activity by 60% and 33% respectively. ASE reduces TC [34%], SOE decreases TG [40%] and LDL [30%] and AAE reduces VLDL [24%]. Metformin exhibits mild antioxidant and hypolipidemic properties. Results of quantitative phytochemical analysis show that the methanolic garlic and Persian shallot bulbs extracts contain secondary metabolites including alkaloids [3.490% and 3.430%], glycosides [18.023% and 13.301%] and saponins [0.812% and 0.752%]. Methanolic sage leaves extract contains flavonoids [1.014%], glycosides [23.142%] and saponins [2.096%]. The total phenolic contents of ASE, AAE and SOE were in order 4.273, 3.621 and 6.548 mg GAE/g dry weight [DW]. These results suggest that Allium sativum, Allium ascalonicum and Salvia officinalis are beneficial in the control of diabetes by noticeable antioxidant and hypolipidemic properties
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Indice: Méditerranée orientale langue: Anglais Texte intégral: Iran. J. Pharm. Res. Année: 2012

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Indice: Méditerranée orientale langue: Anglais Texte intégral: Iran. J. Pharm. Res. Année: 2012