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Liver PPARalpha and UCP2 are involved in the regulation of obesity and lipid metabolism by swim training in genetically obese db/db mice.

作者信息

Oh Ki Sook, Kim Mina, Lee Jinmi, Kim Min Jeong, Nam Youn Shin, Ham Jung Eun, Shin Soon Shik, Lee Chung Moo, Yoon Michung

机构信息

Department of Physical Education, Sookmyung Women's University, Seoul 140-742, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2006 Jul 7;345(3):1232-9. doi: 10.1016/j.bbrc.2006.04.182. Epub 2006 May 15.

DOI:10.1016/j.bbrc.2006.04.182
PMID:16716264
Abstract

Swim training for 6 weeks significantly decreased body weight gain, adipose tissue mass, and adipocyte size in both sexes of genetically obese db/db mice compared with their respective sedentary controls. Swim training also caused significant decreases in serum levels of free fatty acids, triglycerides, and total cholesterol in both sexes of obese mice. Concomitantly, hepatic mRNA levels of peroxisome proliferator-activated receptor alpha (PPARalpha) target enzymes responsible for mitochondrial and peroxisomal fatty acid beta-oxidation were significantly increased by swim training. Moreover, mRNA levels of uncoupling protein 2 (UCP2) in liver were also markedly increased by swim training. In conclusion, these results suggest that swim training-induced transcriptional activation of hepatic PPARalpha target enzymes and UCP2 may effectively prevent body weight gain, adiposity, and lipid disorders caused by leptin receptor deficiency in both sexes of mice.

摘要

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