Altered Pharmacokinetics of Cationic Drugs Caused by Down-Regulation of Renal Rat Organic Cation Transporter 2 (Slc22a2) and Rat Multidrug and Toxin Extrusion 1 (Slc47a1) in Ischemia/Reperfusion-Induced Acute Kidney Injury-Reference-Cited by-同舟云学术

Altered Pharmacokinetics of Cationic Drugs Caused by Down-Regulation of Renal Rat Organic Cation Transporter 2 (Slc22a2) and Rat Multidrug and Toxin Extrusion 1 (Slc47a1) in Ischemia/Reperfusion-Induced Acute Kidney Injury

Published:2008-01-07 Issue:4 Volume:36 Page:649-654
ISSN:0090-9556
Container-title:Drug Metabolism and Disposition
language:en
Short-container-title:Drug Metab Dispos

Author:

Matsuzaki Takanobu,Morisaki Takafumi,Sugimoto Wakako,Yokoo Koji,Sato Daisuke,Nonoguchi Hiroshi,Tomita Kimio,Terada Tomohiro,Inui Ken-ichi,Hamada Akinobu,Saito Hideyuki

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmaceutical Science,Pharmacology

Reference40 articles.

1. Androgen Receptor is Responsible for Rat Organic Cation Transporter 2 Gene Regulation but not for rOCT1 and rOCT3

2. Recent Advances in the Pathophysiology of Ischemic Acute Renal Failure

3. Electrogenic Properties and Substrate Specificity of the Polyspecific Rat Cation Transporter rOCT1

4. Identification and Characterization of Human Organic Anion Transporter 3 Expressing Predominantly in the Kidney

5. Drug excretion mediated by a new prototype of polyspecific transporter

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