有机阳离子转运蛋白
有机阴离子转运蛋白1
运输机
两性离子
溶质载体族
有机阴离子转运多肽
化学
有机阴离子
单胺类神经递质
生物化学
药理学
生物
基因
受体
离子
血清素
分子
有机化学
标识
DOI:10.1016/j.mam.2012.10.010
摘要
The SLC22 family contains 13 functionally characterized human plasma membrane proteins each with 12 predicted α-helical transmembrane domains. The family comprises organic cation transporters (OCTs), organic zwitterion/cation transporters (OCTNs), and organic anion transporters (OATs). The transporters operate as (1) uniporters which mediate facilitated diffusion (OCTs, OCTNs), (2) anion exchangers (OATs), and (3) Na+/zwitterion cotransporters (OCTNs). They participate in small intestinal absorption and hepatic and renal excretion of drugs, xenobiotics and endogenous compounds and perform homeostatic functions in brain and heart. Important endogeneous substrates include monoamine neurotransmitters, l-carnitine, α-ketoglutarate, cAMP, cGMP, prostaglandins, and urate. It has been shown that mutations of the SLC22 genes encoding these transporters cause specific diseases like primary systemic carnitine deficiency and idiopathic renal hypouricemia and are correlated with diseases such as Crohn’s disease and gout. Drug–drug interactions at individual transporters may change pharmacokinetics and toxicities of drugs.
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