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Artigo em Inglês | IMSEAR | ID: sea-151966

RESUMO

This study aimed to evaluate the effects of ethyl acetate and n-butanol fractions of Acacia nilotica methanol leaves extract on lipid profile and liver enzyme on alloxan induced diabetic rats. 30 Wistar rats of both sexes were used for the study. The rats were divided into six groups with five rats in each group. The diabetic rats were treated with n- butanol and ethyl acetate for a period of 12 days. After which the animals were sacrificed and blood serum sample were taken from all the groups for the assessment of lipid profiles and liver enzymes. As regards to the lipid profile there was a significant decrease (P<0.05) in the triglyceride and cholesterol level in ethyl acetate treated group with 50 and 100 mg/kg , while, there was also a significant increase in the levels of high density lipoprotein when compared with the control untreated group. Also there was a significant decrease (P<0.05) in ALT, AST and ALP levels in ethyl acetate fraction treated group with 50 and 100 mg/kg when compared with the control untreated group. In relation to the n-butanol fraction at the two doses tested 100 and 200 mg/kg there was no significant change in the levels of triglyceride when compared with the control untreated. However there was decrease in the levels of cholesterol (p<0.05) and a significant increase in the levels of high density lipoprotein when compared with the control untreated. There was a significant decrease (P<0.05) in the levels of ALT, AST while there was no significant change in the level of ALP treated with the n-butanol fraction when compared with the control untreated group. The phytochemical screening revealed the presences of saponin, flavonoid, tannin and alkaloid. The median lethal dose (LD50) of the ethyl acetate in mice was calculated to be 471.2 mg/kg b.w and n-butanol is 774.5 mg/kg b.w. This results suggest that the Ethylacetate and n-butanol fractions of methanol leaves extract of Acacia nilotica has anti-hyperlipidemic and hepatoprotective effect on alloxan induced diabetic rats.

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