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Model Systems for Studying the Role of Canalicular Efflux Transporters in Drug-Induced Cholestatic Liver Disease

期刊

JOURNAL OF PHARMACEUTICAL SCIENCES
卷 106, 期 9, 页码 2295-2301

出版社

WILEY
DOI: 10.1016/j.xphs.2017.03.023

关键词

Drug interactions; Hepatic transport; Transporters; ABC transporters; Bile acid transporters

资金

  1. Swiss National Science Foundation National Center of Competence in Research TransCure (University of Berne, Switzerland)

向作者/读者索取更多资源

Bile formation is a key function of the liver. Disturbance of bile flow may lead to liver disease and is called cholestasis. Cholestasis may be inherited, for example, in progressive familial intrahepatic cholestasis or acquired, for example, by drug-mediated inhibition of bile salt export from hepatocytes into the canaliculi. The key transport system for exporting bile salts into the canaliculi is the bile salt export pump. Inhibition of the bile salt export pump by drugs is a well-established cause of drug-induced cholestasis. Investigation of the role of the multidrug resistance protein 3, essential for biliary phospholipid secretion, is emerging now. This overview summarizes current concepts and methods with an emphasis on in vitro model systems for the investigation of drug-induced cholestasis in the general context of drug-induced liver injury. (C) 2017 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.

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