High Expression of UGT1A1/1A6 in Monkey Small Intestine: Comparison of Protein Expression Levels of Cytochromes P450, UDP-Glucuronosyltransferases, and Transporters in Small Intestine of Cynomolgus Monkey and Human

被引:30
|
作者
Akazawa, Takanori [1 ]
Uchida, Yasuo [1 ]
Miyauchi, Eisuke [1 ]
Tachikawa, Masanori [1 ]
Ohtsuki, Sumio [2 ]
Terasaki, Tetsuya [1 ]
机构
[1] Tohoku Univ, Div Membrane Transport & Drug Targeting, Grad Sch Pharmaceut Sci, Aoba Ku, 6-3 Aoba, Sendai, Miyagi 9808578, Japan
[2] Kumamoto Univ, Fac Life Sci, Dept Pharmaceut Microbiol, Chuo Ku, 5-1 Oe Honmachi, Kumamoto 8620973, Japan
基金
日本学术振兴会;
关键词
small intestine; drug absorption; cytochromes P450; LTDP-glucuronosyltransferase; transporter; cynomolgus monkey; species differences; protein quantification; quantitative targeted absolute proteomics; TARGETED ABSOLUTE PROTEOMICS; DRUG-METABOLIZING-ENZYMES; CANCER RESISTANCE PROTEIN; MESSENGER-RNA EXPRESSION; BLOOD-BRAIN-BARRIER; ORGANIC SOLUTE TRANSPORTER; P-GLYCOPROTEIN EXPRESSION; ALPHA-OST-BETA; MASS-SPECTROMETRY; QUANTITATIVE ATLAS;
D O I
10.1021/acs.molpharmaceut.7b00772
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cynomolgus monkeys have been widely used for the prediction of drug absorption in humans. The purpose of this study was to clarify the regional protein expression levels of cytochromes 2450 (CYPs), UDP-glucuronosyltransferases (UGTs), and transporters in small intestine of cynomolgus monkey using liquid chromatography-tandem mass spectrometry, and to compare them with the corresponding levels in human. UGT1A1 in jejunum and ileum were >4.57- and >3.11-fold and UGT1A6 in jejunum and ileum were >16.1- and >8.57-fold, respectively, more highly expressed in monkey than in human. Also, jejunal expression of monkey CYP3A8 (homologue of human CYP3A4) was >3.34-fold higher than that of human CYP3A4. Among apical drug efflux transporters, BCRP showed the most abundant expression in monkey and human, and the expression levels of BCRP in monkey and human were >1.74- and >1.25-fold greater than those of P-gp and >2.76- and >4.50-fold greater than those of MRP2, respectively. These findings should be helpful to understand species differences of the functions of CYPs, UGTs, and transporters between monkey and human. The UGT1A1/1A6 data would be especially important because it is difficult to identify isoforms responsible for species differences of intestinal glucuronidation by means of functional studies due to overlapping substrate specificity.
引用
收藏
页码:127 / 140
页数:14
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