PPARα agonists positively and negatively regulate the expression of several nutrient/drug transporters in mouse small intestine

被引:74
作者
Hirai, Toshitake [1 ]
Fukui, Yuka [1 ]
Motojima, Kiyoto [1 ]
机构
[1] Meiji Pharmaceut Univ, Dept Biochem, Tokyo 2048588, Japan
关键词
peroxisome proliferator-activated receptor; transporter; small intestine; microarray; GW7647; drug-drug interaction;
D O I
10.1248/bpb.30.2185
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A systematic analysis to examine the effects of peroxisome proliferator-activated receptor (PPAR)alpha agonists on the expression levels of all the nutrient/drug plasma-membrane transporters in the mouse small intestine was performed. Transporter mRNAs that were induced or repressed by two independent PPAR alpha-specific agonists were identified by a genome-wide microarray method, and the changes were confirmed by real-time PCR using RNA isolated from the intestines and livers of wild-type and PPAR alpha-null mice. Expression levels of seven nutrient/drug transporters (Abcd3, Octn2/Slc22a5, FATP2/Slc27a2, Slc22a21, Mct13/Slc16a13, Slc23a1 and Bcrp/Abcg2) in the intestine were up-regulated and the expression level of one (Mrp1/Abcc1) was down-regulated by PPAR alpha; although the previously report that the H+/peptide co-transporter 1 (Pept1) is up-regulated by PPAR alpha was not replicated in our study. We propose that the transport processes can be coordinately regulated with intracellular metabolism by nutrient nuclear receptors.
引用
收藏
页码:2185 / 2190
页数:6
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