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
相关论文
共 34 条
[1]   Regulation of expression of the intestinal oligopeptide transporter (Pept-1) in health and disease [J].
Adibi, SA .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2003, 285 (05) :G779-G788
[2]   Modulation of nitrated lipid signaling by multidrug resistance protein 1 (MRP1):: Glutathione conjugation and MRP1-mediated efflux inhibit nitrolinoleic acid-induced, PPARγ-dependent transcription activation [J].
Alexander, Richard L. ;
Bates, Darcy J. P. ;
Wright, Marcus W. ;
King, S. Bruce ;
Morrow, Charles S. .
BIOCHEMISTRY, 2006, 45 (25) :7889-7896
[3]   Identification of ERRα as a specific partner of PGC-1α for the activation of PDK4 gene expression in muscle [J].
Araki, M ;
Motojima, K .
FEBS JOURNAL, 2006, 273 (08) :1669-1680
[4]   Direct evidence for peptide transporter (PepT1)-mediated uptake of a nonpeptide prodrug, valacyclovir [J].
Balimane, PV ;
Tamai, I ;
Guo, AL ;
Nakanishi, T ;
Kitada, H ;
Leibach, FH ;
Tsuji, A ;
Sinko, PJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 250 (02) :246-251
[5]   Biology of a novel organic solute and steroid transporter, OSTα-OSTβ [J].
Ballatori, N .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2005, 230 (10) :689-698
[6]   Endothelial cell apoptosis induced by the peroxisome proliferator-activated receptor (PPAR) ligand 15-deoxy-Δ12,14-prostaglandin J2 [J].
Bishop-Bailey, D ;
Hla, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (24) :17042-17048
[7]   Identification of a subtype selective human PPARα agonist through parallel-array synthesis [J].
Brown, PJ ;
Stuart, LW ;
Hurley, KP ;
Lewis, MC ;
Winegar, DA ;
Wilson, JG ;
Wilkinson, WO ;
Ittoop, OR ;
Willson, TM .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2001, 11 (09) :1225-1227
[8]   Genome-wide analysis of PPARα activation in murine small intestine [J].
Bunger, Meike ;
van den Bosch, Heleen M. ;
van der Meijde, Jolanda ;
Kersten, Sander ;
Hooiveld, Guido J. E. J. ;
Muller, Michael .
PHYSIOLOGICAL GENOMICS, 2007, 30 (02) :192-204
[9]   Genetic basis of toxic reactions to drugs and chemicals [J].
Cascorbi, I .
TOXICOLOGY LETTERS, 2006, 162 (01) :16-28
[10]   Role of pharmacogenetics of ATP-binding cassette transporters in the pharmacokinetics of drugs [J].
Cascorbi, Ingolf .
PHARMACOLOGY & THERAPEUTICS, 2006, 112 (02) :457-473