Drug Transporters in the Central Nervous System

被引:40
作者
Stieger, Bruno [1 ]
Gao, Bo [1 ]
机构
[1] Univ Zurich Hosp, Dept Clin Pharmacol & Toxicol, CH-8091 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
BLOOD-BRAIN-BARRIER; ORGANIC ANION TRANSPORTER; RESISTANCE-ASSOCIATED PROTEIN; RAT CHOROID-PLEXUS; CAPILLARY ENDOTHELIAL-CELLS; CEREBROSPINAL FLUID BARRIER; P-GLYCOPROTEIN EXPRESSION; RETINAL-PIGMENT EPITHELIUM; HUMAN OCULAR-TISSUES; ACETYL-L-CARNITINE;
D O I
10.1007/s40262-015-0241-y
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drug targets in the central nervous system (CNS) are numerous and important for drug therapy, e.g., of epilepsy or pain. Drugs and other xenobiotics as well as nutrients cannot freely cross the blood-brain barrier or freely enter cells across plasma membranes and therefore require transport systems. This overview summarizes the current knowledge on the expression of drug transporters in barriers shielding the CNS from the systemic circulation and as such controlling the pharmacokinetics of drugs in the CNS. The main drug transporter families covered are SLCO, SCL22A, ABCB, and ABCC, as genes of these families code for numerous drug transporters. While knowledge on messenger RNA expression in humans, rats, and mice is remarkable, there is clearly a gap in knowledge on the subcellular expression of transporters in specific cells in the CNS and in the barriers shielding the CNS from the systemic circulation. Recent methodologic developments including synthesis of drugs and endogenous substances for imaging will in the future allow the investigation of the function and physiologic role of transporters in the CNS including difficult-to-access systems such as the choroid plexus.
引用
收藏
页码:225 / 242
页数:18
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