Physiology and Pathophysiology of the Blood-Brain Barrier: P-Glycoprotein and Occludin Trafficking as Therapeutic Targets to Optimize Central Nervous System Drug Delivery

被引:27
作者
McCaffrey, Gwen [1 ]
Davis, Thomas P. [1 ]
机构
[1] Univ Arizona, Coll Med, Dept Med Pharmacol, Tucson, AZ 85745 USA
基金
美国国家卫生研究院;
关键词
blood-brain barrier; CNS drug delivery; protein trafficking; protein-protein interaction; oxidative stress; peripheral inflammatory pain; P-glycoprotein; occludin; PROTEIN-PROTEIN INTERACTIONS; CELL-PENETRATING PEPTIDES; INHIBITOR STARTING POINTS; TIGHT JUNCTIONS; MULTIDRUG-RESISTANCE; ENDOTHELIAL-CELLS; INFLAMMATORY PAIN; ABC TRANSPORTERS; INTRACELLULAR TRAFFICKING; OLIGOMERIC ASSEMBLIES;
D O I
10.2310/JIM.0b013e318276de79
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The blood-brain barrier (BBB) is a physical and metabolic barrier that separates the central nervous system from the peripheral circulation. Central nervous system drug delivery across the BBB is challenging, primarily because of the physical restriction of paracellular diffusion between the endothelial cells that comprise the microvessels of the BBB and the activity of efflux transporters that quickly expel back into the capillary lumen a wide variety of xenobiotics. Therapeutic manipulation of protein trafficking is emerging as a novel means of modulating protein function, and in this minireview, the targeting of the trafficking of 2 key BBB proteins, P-glycoprotein and occludin, is presented as a novel, reversible means of optimizing central nervous system drug delivery.
引用
收藏
页码:1131 / 1140
页数:10
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