Protective Effects of Voluntary Exercise on Hepatic Fat Accumulation Induced by Dietary Restriction in Zucker Fatty Rats

Weight control based on dietary restriction (DR) alone can cause lipid metabolic failure and progression to fatty liver. This study aimed to investigate the effect of exercise on preventing DR-induced hepatic fat accumulation in Zucker fatty (ZF) rats by focusing on the relationship between adipose...

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Veröffentlicht in:International journal of molecular sciences 2021-02, Vol.22 (4), p.2014
Hauptverfasser: Kurosaka, Yuka, Machida, Shuichi, Shiroya, Yoko, Yamauchi, Hideki, Minato, Kumiko
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Sprache:eng
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Zusammenfassung:Weight control based on dietary restriction (DR) alone can cause lipid metabolic failure and progression to fatty liver. This study aimed to investigate the effect of exercise on preventing DR-induced hepatic fat accumulation in Zucker fatty (ZF) rats by focusing on the relationship between adipose tissue lipolysis and hepatic fat uptake. Six-week-old male ZF rats were randomly assigned to obese, DR, or DR with exercise (DR + Ex) groups. The DR and DR + Ex groups were fed a restricted diet, with the latter also undergoing voluntary exercise. After 6 weeks, hepatic fat accumulation was observed in the DR group, whereas intrahepatic fat was markedly reduced in the DR + Ex group. Compared with the obese (Ob) group, the DR group exhibited 2.09-fold expression of hepatic fatty acid translocase (FAT)/CD36 proteins ( < 0.01) and 0.14-fold expression of hepatic fatty acid-binding protein (FABP)1 ( < 0.01). There were no significant differences between the DR + Ex group and the Ob group. FAT/CD36 and hepatic triglyceride (TG) expression levels were strongly positively correlated ( = 0.81, < 0.001), whereas there was a strong negative correlation between FABP1 and hepatic TG expression levels ( = -0.65, < 0.001). Our results suggest that hepatic fat accumulation induced by DR in ZF rats might be prevented through exercise-induced modifications in FAT/CD36 and FABP1 expression.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms22042014