Effect of Caloric Restriction and AMPK Activation on Hepatic Nuclear Receptor, Biotransformation Enzyme, and Transporter Expression in Lean and Obese Mice

被引:9
作者
Kulkarni, Supriya R. [1 ]
Xu, Jialin [1 ]
Donepudi, Ajay C. [1 ]
Wei, Wei [1 ]
Slitt, Angela L. [1 ]
机构
[1] Univ Rhode Isl, Coll Pharm, Dept Biomed & Pharmaceut Sci, Kingston, RI 02881 USA
关键词
gene expression; liver; nuclear receptor; steatosis; transport; FATTY LIVER-DISEASE; PROTEIN-KINASE; LIPID-METABOLISM; MOUSE-LIVER; PPAR-ALPHA; PHASE-I; SIRT1; RESISTANCE; INDUCTION; LEPTIN;
D O I
10.1007/s11095-013-1140-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fatty liver alters liver transporter expression. Caloric restriction (CR), the recommended therapy to reverse fatty liver, increases Sirtuin1 deacetylase activity in liver. This study evaluated whether CR and CR mimetics reversed obesity-induced transporter expression in liver and hepatocytes. mRNA and protein expression was determined in adult lean (lean) and leptin-deficient obese (OB) mice fed ad libitum or placed on 40% (kCal) reduced diet. Hepatocytes were isolated from lean and OB mice, treated with AMP Kinase activators, and gene expression was determined. CR decreased Oatp1a1, Oatp1b2, and Abcb11 mRNA expression in lean, but not OB mice. CR increased Abcc2 mRNA OB livers, whereas protein expression increased in both genotypes. CR increased Abcc3 protein expression increased in OB livers. CR did not alter Abcc1, 4 and 5 mRNA expression in lean mice but decreased expression in livers of OB mice. CR increased Abcc4 protein in lean, but not OB mice. CR restriction reversed the expression of some, but not all transporters in livers of OB mice. Overall, these data indicate a potential for CR to restore some hepatic transporter changes in OB mice, but suggest a functional leptin axis is needed for reversal of expression for some transporters.
引用
收藏
页码:2232 / 2247
页数:16
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