Xie Hui, Lu Wei-Cheng
Department of Histology and Embryology, College of Basic Medicine, Shenyang Medical College, Shenyang, China.
Department of Neurosurgery, First Affiliated Hospital of China Medical University, Shenyang, China.
Neuropathology. 2018 Apr 17. doi: 10.1111/neup.12469.
This study aimed to investigate the effects of transient receptor potential vanilloid 4 (TRPV4) inhibition on blood-brain barrier (BBB) integrity and the expressions of caveolae structural proteins caveolin-1 and caveolin-2 in rats with focal cerebral ischemia and reperfusion. BBB permeability was assessed by Evans blue extravasation. The mRNA and protein expressions of caveolin-1 and caveolin-2 were determined by RT-PCR, Western blot and immunohistochemistry assays. We found that BBB permeability significantly increased and reaches its peak at 72 h of reperfusion in cerebral ischemia-reperfusion rats and is able to be ameliorated by administration of HC-067047, an antagonist of TRPV4. Additionally, it shows a significant upregulation of caveolin-1 and caveolin-2 expression in cerebral microvessels of ischemic tissue. However, treatment with HC-067047 was shown to downregulate caveolin-1 and caveolin-2 expression during cerebral ischemia-reperfusion. This study demonstrates that inhibition of TRPV4 ameliorates BBB leakage induced by ischemia-reperfusion injury through the downregulation of caveolin-1 and caveolin-2.
本研究旨在探讨瞬时受体电位香草酸受体4(TRPV4)抑制对局灶性脑缺血再灌注大鼠血脑屏障(BBB)完整性以及小窝结构蛋白小窝蛋白-1和小窝蛋白-2表达的影响。通过伊文思蓝外渗评估BBB通透性。采用逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹法和免疫组织化学分析检测小窝蛋白-1和小窝蛋白-2的mRNA及蛋白表达。我们发现,在脑缺血再灌注大鼠中,BBB通透性显著增加,并在再灌注72小时达到峰值,而给予TRPV4拮抗剂HC-067047可使其改善。此外,缺血组织脑微血管中小窝蛋白-1和小窝蛋白-2的表达显著上调。然而,在脑缺血再灌注期间,HC-067047治疗显示可下调小窝蛋白-1和小窝蛋白-2的表达。本研究表明,抑制TRPV4可通过下调小窝蛋白-1和小窝蛋白-2改善缺血再灌注损伤诱导的BBB渗漏。