Back to Search Start Over

All-Trans Retinoic Acid (atRA) effectively improves liver steatosis in a rabbit model of high fat induced liver steatosis.

Authors :
Zarei, Leila
Farhad, Negin
Abbasi, Ata
Source :
Archives of Physiology & Biochemistry; Aug2022, Vol. 128 Issue 4, p1010-1015, 6p
Publication Year :
2022

Abstract

The aim of this study is to evaluate the role of All-Trans Retinoic Acid, the biologically active metabolite of retinoids, on liver steatosis in a rabbit model of high fat induced lever steatosis. 30 male rabbits were evaluated in 5 groups: group 1 treated with normal diet, group 2–5 included rabbit's groups 2 to 5 were fed on high cholesterol diet, group 2 received no drugs, group 3 received atorvastatin, group 4 received atRA, and group 5 received both the drugs. the liver was obtained for histopathological evaluation. oral administration of atRA, atorvastatin or their combination significantly decreased serum levels of total cholesterol, LDL, AST and ALT. atorvastatin slightly but atRA remarkably decreased liver steatosis where the difference was significant. atRA group showed the highest TAC and the lowest PCO concentrations. atRA can be effective in reducing liver steatosis and its antioxidant effect plays a crucial role in the process. Non-alcoholic fatty liver disease (NAFLD) is the most common disorder of the liver in general population and is strongly associated with metabolic risk factors including hyperlipidaemia, obesity and diabetes. atRA is very effective in reducing liver steatosis and its antioxidant effect plays a crucial role in the process. we suggest focussing on other aspects of liver steatosis such as carbohydrate metabolism and insulin resistance in order to find better ways of controlling and treating liver steatosis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13813455
Volume :
128
Issue :
4
Database :
Complementary Index
Journal :
Archives of Physiology & Biochemistry
Publication Type :
Academic Journal
Accession number :
158319926
Full Text :
https://doi.org/10.1080/13813455.2020.1743725