Involvement of Organic Cation Transporters in the Kinetics of Trimethylamine N-oxide

被引:34
作者
Miyake, Takeshi [1 ]
Mizuno, Tadahaya [1 ]
Mochizuki, Tatsuki [1 ]
Kimura, Miyuki [2 ]
Matsuki, Shunji [2 ]
Irie, Shin [2 ]
Ieiri, Ichiro [3 ]
Maeda, Kazuya [1 ]
Kusuhara, Hiroyuki [1 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Mol Pharmacokinet, Bunkyo Ku, Tokyo 1130033, Japan
[2] Fukuoka Mirai Hosp, Clin Res Ctr, Fukuoka 8130017, Japan
[3] Kyushu Univ, Grad Sch Pharmaceut Sci, Dept Clin Pharmacokinet, Fukuoka 8128582, Japan
关键词
organic cation transporters (OCTs); renal clearance; hepatic transport; hepatocytes; elderly; FUNCTIONAL-CHARACTERIZATION; GUT MICROBIOTA; HEPATIC-UPTAKE; METABOLISM; EXPRESSION; EXCRETION; PHOSPHATIDYLCHOLINE; DYSFUNCTION; SECRETION; MICE;
D O I
10.1016/j.xphs.2017.04.067
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Recent studies suggest that trimethylamine N-oxide (TMAO) is associated with the development of chronic kidney disease and heart failure. In this study, we investigated the importance of organic cation transporters (OCTs) in the clearance and tissue distribution of TMAO. The low-affinity and high-capacity transport of TMAO by mouse and human OCT1 and OCT2 was observed. Uptake and efflux of TMAO by the mouse hepatocytes as well as TMAO uptake into mouse kidney slices were significantly decreased by the addition of tetraethylammonium or Oct1/2 double knockout (dKO). Plasma concentrations of endogenous TMAO and TMAO-d9 given by intravenous infusion was 2-fold higher in Oct1/2 dKO than in wild-type mice due to significant decrease in its renal clearance. These results indicate that OCTs have a crucial role in the kinetics of TMAO in mice. In human, however, the OCT2-mediated tubular secretion in the urinary excretion of TMAO was insignificant because the renal clearance of TMAO was similar to that of creatinine in both young and elderly subjects, suggesting the species difference in the urinary excretion mechanisms of TMAO between mouse and human. (C) 2017 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:2542 / 2550
页数:9
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