Dietary lipids regulate β-oxidation enzyme gene expression in the developing rat kidney

被引:47
作者
Ouali, F [1 ]
Djouadi, F [1 ]
Merlet-Benichou, C [1 ]
Bastin, J [1 ]
机构
[1] Univ Paris 07, INSERM U319, F-75251 Paris 05, France
关键词
energy metabolism; postnatal period; mitochondria; peroxisome; gene regulation; peroxisome proliferator-activated receptor;
D O I
10.1152/ajprenal.1998.275.5.F777
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
This study examines the ability of dietary lipids to regulate gene expression of mitochondrial and peroxisomal fatty acid beta-oxidation enzymes in the kidney cortex and medulla of 3-wk-old rats and evaluates the role of glucagon or of the alpha-isoform of peroxisome proliferator-activated receptor (PPAR alpha) in mediating beta-oxidation enzyme gene regulation in the immature kidney. The long-chain (LCAD) and medium-chain acyl-CoA dehydrogenases (MCAD) and acyl-CoA oxidase (ACO) mRNA levels were found coordinately upregulated in renal cortex, but not in medulla, of pups weaned on a high-fat diet from day 16 to 21. Further results establish that switching pups from a low to a high-fat diet for only 1 day was sufficient to induce large increases in cortical LCAD, MCAD, and ACO mRNA levels, and gavage experiments show that this upregulation of beta-oxidation gene expression is initiated within 6 h following lipid ingestion. Treatment of pups with clofibrate, a PPAR alpha agonist, demonstrated that PPAR alpha can mediate regulation of cortical beta-oxidation enzyme gene expression, whereas glucagon was found ineffective. Thus dietary Lipids physiologically regulate gene expression of mitochondrial and peroxisomal beta-oxidation enzymes in the renal cortex of suckling pups, and this might involve PPAR alpha-mediated mechanisms.
引用
收藏
页码:F777 / F784
页数:8
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