Effects of resveratrol, exercises and their combination on Farnesoid X receptor, Liver X receptor and Sirtuin 1 gene expression and apoptosis in the liver of elderly rats with nonalcoholic fatty liver

Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disorder. This study aims to consider effects of resveratrol, exercise and their combination on genes expression in the liver of elderly rats with NAFLD. Rats with NAFLD were randomly divided into seven groups including patie...

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Published in:PeerJ (San Francisco, CA) Vol. 6; p. e5522
Main Authors: Hajighasem, Amir, Farzanegi, Parvin, Mazaheri, Zohreh, Naghizadeh, Marjan, Salehi, Ghoncheh
Format: Journal Article
Language:English
Published: United States PeerJ, Inc 10-09-2018
PeerJ Inc
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Summary:Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disorder. This study aims to consider effects of resveratrol, exercise and their combination on genes expression in the liver of elderly rats with NAFLD. Rats with NAFLD were randomly divided into seven groups including patient, saline, resveratrol (RSV), interval exercise, continuous exercise, interval exercise + RSV and continuous exercise + RSV. Levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP) in the liver tissue were measured using specific ELISA kits. A TUNEL assay kit was used for the assessment of hepatic cells apoptosis. Lipid profiles were considered by measuring the serum triglyceride, cholesterol, LDL, and HDL. Expression of , and genes was considered using RT-PCR. Resveratrol administration alone or combined with exercise training significantly improved the expression of , and genes (  < 0.05) in the hepatic tissue of rats with NAFLD, while levels of AST, ALT, ALP enzymes, as well as apoptotic cells were significantly decreased (  < 0.05). Although resveratrol alone improves the expression of , and , as well as liver function, combined therapy with exercise training is more effective to improve NAFLD.
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ISSN:2167-8359
2167-8359
DOI:10.7717/peerj.5522