Comparative gene expression of intestinal metabolizing enzymes

• Published in: Biopharmaceutics & drug disposition 2009-11, Vol.30 (8), p.411-421
• Main Authors: Shin, Ho-Chul, Kim, Hye-Ryoung, Cho, Hee-Jung, Yi, Hee, Cho, Soo-Min, Lee, Dong-Goo, Abd El-Aty, A. M., Kim, Jin-Suk, Sun, Duxin, Amidon, Gordon L.
• Format: Article
• Language: English
• Subjects: Animals; Cytochrome P-450 CYP3A - genetics; Cytochrome P-450 CYP3A - metabolism; Cytochrome P-450 Enzyme System - genetics; Cytochrome P-450 Enzyme System - metabolism; Gene Expression; Gene Expression Profiling; Glucuronosyltransferase - metabolism; Humans; intestine; Intestines - enzymology; Intestines - metabolism; metabolizing enzymes; Mice; Microsomes, Liver - enzymology; Microsomes, Liver - metabolism; mouse/rat/human; Pharmaceutical Preparations - metabolism; Rats
• ISSN: 0142-2782; 1099-081X
• DOI: 10.1002/bdd.675

The purpose of this study was to compare the expression profiles of drug‐metabolizing enzymes in the intestine of mouse, rat and human. Total RNA was isolated from the duodenum and the mRNA expression was measured using Affymetrix GeneChip oligonucleotide arrays. Detected genes from the intestine of mouse, rat and human were ca. 60% of 22690 sequences, 40% of 8739 and 47% of 12559, respectively. Total genes of metabolizing enzymes subjected in this study were 95, 33 and 68 genes in mouse, rat and human, respectively. Of phase I enzymes, the mouse exhibited abundant gene expressions for Cyp3a25, Cyp4v3, Cyp2d26, followed by Cyp2b20, Cyp2c65 and Cyp4f14, whereas, the rat showed higher expression profiles of Cyp3a9, Cyp2b19, Cyp4f1, Cyp17a1, Cyp2d18, Cyp27a1 and Cyp4f6. However, the highly expressed P450 enzymes were CYP3A4, CYP3A5, CYP4F3, CYP2C18, CYP2C9, CYP2D6, CYP3A7, CYP11B1 and CYP2B6 in the human. For phase II enzymes, glucuronosyltransferase Ugt1a6, glutathione S‐transferases Gstp1, Gstm3 and Gsta2, sulfotransferase Sult1b1 and acyltransferase Dgat1 were highly expressed in the mouse. The rat revealed predominant expression of glucuronosyltransferases Ugt1a1 and Ugt1a7, sulfotransferase Sult1b1, acetyltransferase Dlat and acyltransferase Dgat1. On the other hand, in human, glucuronosyltransferases UGT2B15 and UGT2B17, glutathione S‐transferases MGST3, GSTP1, GSTA2 and GSTM4, sulfotransferases ST1A3 and SULT1A2, acetyltransferases SAT1 and CRAT, and acyltransferase AGPAT2 were dominantly detected. Therefore, current data indicated substantial interspecies differences in the pattern of intestinal gene expression both for P450 enzymes and phase II drug‐metabolizing enzymes. This genomic database is expected to improve our understanding of interspecies variations in estimating intestinal prehepatic clearance of oral drugs. Copyright © 2009 John Wiley & Sons, Ltd.