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Antihyperlipidemic potential of diosmin in Swiss Albino mice with high-fat diet induced hyperlipidemia

Authors :
Sayeed Mohammed Firdous
Mourad A. M. Aboul-Soud
Gaber E. El-Desouky
Sayan Hazra
Subash C. B. Gopinath
Source :
Saudi Journal of Biological Sciences, Saudi Journal of Biological Sciences, Vol 28, Iss 1, Pp 109-115 (2021)
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

This study was aimed to investigate the antihyperlipidemic potential of Diosmin (DS) in mice fed with a high-fat diet (HFD). Animals were divided in five groups (n=6). The total duration of the study was 90 days split into two intervals. During the first 45-day interval, mice were administered with HFD, whereas during the second 45-day interval they were co-administered HFD plus DS or the standard drug atorvastatin. DS was administered at the dose of 100 and 200 mg/kg;p.o. DS treatment to HFD-induced hyperlipidemic mice caused significant decrements in the levels of total cholesterol, triglycerides, LDL-C and VLDL-C. Moreover, DS resulted in significant increase in the levels of HDL-C and improvements in total protein levels, whereas it caused remarkable decreases in SGOT, SGPT and ALP enzymatic activities in hyperlipidemic mice. Histopathological examination of hyperlipidemic mice revealed a disorganized hepatic tissue, fatty changes, and mononuclear cell infiltration, which were all ameliorated by DS administration. The results revealed that DS possesses potential ameliorating benefits against hyperlipidemia induced by HFD on lipid profile, liver function enzymes and hepatic histoarchitecture. Further investigations are highly recommended and clinical trials are warranted in order to assess the efficacy and to fully dissect the mode-of-action underpinning the observed antihyperlipidemic effect of DS.

Details

ISSN :
1319562X
Volume :
28
Database :
OpenAIRE
Journal :
Saudi Journal of Biological Sciences
Accession number :
edsair.doi.dedup.....81d60083cd17def767ce56c49ec16ff8
Full Text :
https://doi.org/10.1016/j.sjbs.2020.08.040