Department of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, ON, M5S 3M2, Canada.
Trends Pharmacol Sci. 2013 Jul;34(7):361-72. doi: 10.1016/j.tips.2013.05.004. Epub 2013 Jun 13.
ATP-binding cassette membrane-associated drug efflux transporters and solute carrier influx transporters, expressed at the blood-brain barrier, blood-cerebrospinal fluid barrier, and in brain parenchyma, are important determinants of drug disposition in the central nervous system. Targeting the regulatory pathways that govern the expression of these transporters could provide novel approaches to selectively alter drug permeability into the brain. Nuclear receptors are ligand-activated transcription factors which regulate the gene expression of several metabolic enzymes and drug efflux/influx transporters. Although efforts have primarily been focused on investigating these regulatory pathways in peripheral organs (i.e., liver and intestine), recent findings demonstrate their significance in the brain. This review addresses the role of nuclear receptors in the regulation of drug transporter functional expression in the brain. An in-depth understanding of these pathways could guide the development of novel pharmacotherapy with either enhanced efficacy in the central nervous system or minimal associated neurotoxicity.
ATP 结合盒膜相关药物外排转运体和溶质载体摄取转运体,在血脑屏障、血脑脊液屏障和脑实质中表达,是影响药物在中枢神经系统中分布的重要决定因素。针对调节这些转运体表达的调控途径,可能为选择性改变药物向脑内渗透提供新的方法。核受体是配体激活的转录因子,可调节多种代谢酶和药物外排/摄取转运体的基因表达。虽然主要集中在研究这些在周围器官(即肝脏和肠道)中的调控途径,但最近的研究结果表明它们在大脑中的重要性。本文综述了核受体在调节脑内药物转运体功能表达中的作用。深入了解这些途径可以指导新型药物治疗的发展,在中枢神经系统中具有增强的疗效或最小的神经毒性。