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药物跨肝血窦膜的转运:肝脏中血窦药物的流入与流出

Transport of drugs across the hepatic sinusoidal membrane: sinusoidal drug influx and efflux in the liver.

作者信息

Suzuki H, Sugiyama Y

机构信息

Graduate School of Pharmaceutical Sciences, University of Tokyo, Japan.

出版信息

Semin Liver Dis. 2000;20(3):251-63. doi: 10.1055/s-2000-8408.

Abstract

The liver plays an important role in the detoxification of xenobiotics. Recently, many secondary active transporters responsible for sinusoidal drug uptake have been cloned and their transport properties have been determined. These include rat and human Na(+)-taurocholate cotransporting polypeptides, rat and human organic anion transporting polypeptides, rat and human prostaglandin transporters, rat organic anion transporters, and rat and human organic cation transporters. In addition, it has been suggested that the expression of multi-drug resistance associated protein 3, a primary active transporter responsible for the cellular extrusion of organic anions, on the sinusoidal membrane is induced under cholestatic conditions. In this article, drug transport across the sinusoidal membrane is summarized, particularly focusing on the molecular mechanism of transport.

摘要

肝脏在异生素的解毒过程中发挥着重要作用。最近,许多负责窦状隙药物摄取的次级主动转运蛋白已被克隆,其转运特性也已确定。这些包括大鼠和人类的钠-牛磺胆酸盐共转运多肽、大鼠和人类的有机阴离子转运多肽、大鼠和人类的前列腺素转运蛋白、大鼠有机阴离子转运蛋白以及大鼠和人类的有机阳离子转运蛋白。此外,有人提出,在胆汁淤积条件下,窦状隙膜上负责有机阴离子细胞外排的初级主动转运蛋白——多药耐药相关蛋白3的表达会被诱导。在本文中,将总结药物跨窦状隙膜的转运情况,尤其关注转运的分子机制。

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