Miyazaki Hiroki, Sekine Takashi, Endou Hitoshi
Department of Pharmacology and Toxicology, Kyorin University School of Medicine, 6-20-2, Shinkawa, Mitaka-shi, Tokyo 181-8611, Japan.
Trends Pharmacol Sci. 2004 Dec;25(12):654-62. doi: 10.1016/j.tips.2004.10.006.
Physiological and pharmacological studies indicate that the renal and hepatic organic anion transport systems are responsible for the elimination of numerous compounds, such as drugs, environmental substances and metabolites of both endogenous and exogenous origins. Recently, the molecular identity of the organic anion transport system, the OAT family, was revealed. To date, six OAT members have been identified and shown to have important roles not only in detoxification in the kidneys, liver and brain, but also in the reabsorption of essential compounds such as urate. The OAT family members are closely associated with the pharmacokinetics, drug-drug interactions and toxicity of anionic substances such as nephrotoxic drugs and uremic toxins. The molecular characterization of the OAT family encoded by SLC22A will be discussed.
生理学和药理学研究表明,肾脏和肝脏的有机阴离子转运系统负责清除众多化合物,如药物、环境物质以及内源性和外源性来源的代谢产物。最近,有机阴离子转运系统即OAT家族的分子特性被揭示。迄今为止,已鉴定出六个OAT成员,它们不仅在肾脏、肝脏和大脑的解毒过程中发挥重要作用,而且在尿酸等必需化合物的重吸收中也起重要作用。OAT家族成员与肾毒性药物和尿毒症毒素等阴离子物质的药代动力学、药物相互作用及毒性密切相关。将讨论由SLC22A编码的OAT家族的分子特征。