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Comparative gene expression of intestinal metabolizing enzymes

dc.contributor.authorShin, Ho-Chulen_US
dc.contributor.authorKim, Hye-Ryoungen_US
dc.contributor.authorCho, Hee-Jungen_US
dc.contributor.authorYi, Heeen_US
dc.contributor.authorCho, Soo-Minen_US
dc.contributor.authorLee, Dong-Gooen_US
dc.contributor.authorAbd El-Aty, A. M.en_US
dc.contributor.authorKim, Jin-Suken_US
dc.contributor.authorSun, Duxinen_US
dc.contributor.authorAmidon, Gordon L.en_US
dc.date.accessioned2009-11-06T16:49:19Z
dc.date.available2010-03-01T21:10:29Zen_US
dc.date.issued2009-11en_US
dc.identifier.citationShin, 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. (2009). "Comparative gene expression of intestinal metabolizing enzymes." Biopharmaceutics & Drug Disposition 30(8): 411-421. <http://hdl.handle.net/2027.42/64317>en_US
dc.identifier.issn0142-2782en_US
dc.identifier.issn1099-081Xen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/64317
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=19746353&dopt=citationen_US
dc.description.abstractThe 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.en_US
dc.format.extent223956 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.subject.otherChemistryen_US
dc.subject.otherFood Science, Agricultural, Medicinal and Pharmaceutical Chemistryen_US
dc.titleComparative gene expression of intestinal metabolizing enzymesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationotherDepartment of Veterinary Pharmacology and Toxicology, Konkuk University, Seoul 143-701, Republic of Korea ; Department of Veterinary Pharmacology and Toxicology, Konkuk University, Seoul 143-701, Republic of Koreaen_US
dc.contributor.affiliationotherDepartment of Veterinary Pharmacology and Toxicology, Konkuk University, Seoul 143-701, Republic of Koreaen_US
dc.contributor.affiliationotherDepartment of Veterinary Pharmacology and Toxicology, Konkuk University, Seoul 143-701, Republic of Koreaen_US
dc.contributor.affiliationotherDepartment of Veterinary Pharmacology and Toxicology, Konkuk University, Seoul 143-701, Republic of Koreaen_US
dc.contributor.affiliationotherDepartment of Veterinary Pharmacology and Toxicology, Konkuk University, Seoul 143-701, Republic of Koreaen_US
dc.contributor.affiliationotherDepartment of Veterinary Pharmacology and Toxicology, Konkuk University, Seoul 143-701, Republic of Koreaen_US
dc.contributor.affiliationotherDepartment of Veterinary Pharmacology and Toxicology, Konkuk University, Seoul 143-701, Republic of Koreaen_US
dc.contributor.affiliationotherDepartment of Veterinary Pharmacology and Toxicology, Konkuk University, Seoul 143-701, Republic of Koreaen_US
dc.identifier.pmid19746353en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/64317/1/675_ftp.pdf
dc.identifier.doi10.1002/bdd.675en_US
dc.identifier.sourceBiopharmaceutics & Drug Dispositionen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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