Sandoval Karin E, Witt Ken A
Department of Pharmaceutical Sciences, School of Pharmacy, Southern Illinois University Edwardsville, Edwardsville, IL 62026, USA.
Neurobiol Dis. 2008 Nov;32(2):200-19. doi: 10.1016/j.nbd.2008.08.005. Epub 2008 Aug 27.
The blood-brain barrier (BBB) is formed by the endothelial cells of cerebral microvessels, providing a dynamic interface between the peripheral circulation and the central nervous system. The tight junctions (TJs) between the endothelial cells serve to restrict blood-borne substances from entering the brain. Under ischemic stroke conditions decreased BBB TJ integrity results in increased paracellular permeability, directly contributing to cerebral vasogenic edema, hemorrhagic transformation, and increased mortality. This loss of TJ integrity occurs in a phasic manner, which is contingent on several interdependent mechanisms (ionic dysregulation, inflammation, oxidative and nitrosative stress, enzymatic activity, and angiogenesis). Understanding the inter-relation of these mechanisms is critical for the development of new therapies. This review focuses on those aspects of ischemic stroke impacting BBB TJ integrity and the principle regulatory pathways, respective to the phases of paracellular permeability.
血脑屏障(BBB)由脑微血管内皮细胞形成,在周围循环和中枢神经系统之间提供一个动态界面。内皮细胞之间的紧密连接(TJ)可限制血源物质进入大脑。在缺血性中风情况下,血脑屏障紧密连接完整性降低会导致细胞旁通透性增加,直接导致脑血管源性水肿、出血性转化和死亡率增加。紧密连接完整性的丧失呈阶段性发生,这取决于几种相互依存的机制(离子失调、炎症、氧化和亚硝化应激、酶活性和血管生成)。了解这些机制之间的相互关系对于开发新疗法至关重要。本综述重点关注缺血性中风影响血脑屏障紧密连接完整性的那些方面以及与细胞旁通透性各阶段相关的主要调节途径。