He Fangyan, Duan Xiaohua, Dai Rong, Li Yan, Lin Qing
The Department of Pharmacology, Yunnan University of Traditional Chinese Medicine, Kunming, China.
The Key Modern Research Laboratory for Ethno-Pharmacognosy of Yunnan Higher School, Yunnan University of Traditional Chinese Medicine, Kunming, China.
J Stroke Cerebrovasc Dis. 2017 Jun;26(6):1258-1265. doi: 10.1016/j.jstrokecerebrovasdis.2017.01.018. Epub 2017 Apr 7.
Damage of the blood-brain barrier (BBB) during the process of cerebral ischemic injury is a key factor that influences the therapeutic efficacy to the cerebral ischemic injury. This work was designed to investigate the mechanisms underlying the protective effects of 4-methoxy benzyl alcohol (4-MA) on the BBB by developing a cerebral ischemia/reperfusion model of rats (MCAO/R). The MCAO/R was developed through a thread embolism method. The neurologic scales, the brain infarct rate, and the Evans blue (EB) contents of the brains were detected. Meanwhile, the release of nitric oxide (NO) and activities of NO synthase (NOS) in brain tissues were measured. Western blotting analyses were also used to assess the protein expressions of aquaporin-4 (AQP-4), occludin, and claudin-5 in brain tissue. After rats were pretreated with different concentrations of 4-MA, the neurologic scores, the infarct rate, and the EB contents in the brain tissues were significantly decreased. The release of NO and the activities of neuronal NOS and inducible NOS were notably inhibited. Furthermore, the protein expression of AQP-4 was markedly decreased, whereas the protein expressions of claudin-5 and occludin were significantly increased. In conclusion, the 4-MA decreases the permeability of BBB when focal cerebral ischemia occurs. The inhibition of the NOS pathways, the attenuation of the protein expression of AQP-4, and the enhancement of the expressions of the tight junction proteins might contribute to the protective effects of 4-MA on the BBB.
脑缺血损伤过程中血脑屏障(BBB)的破坏是影响脑缺血损伤治疗效果的关键因素。本研究旨在通过建立大鼠脑缺血/再灌注模型(MCAO/R),探讨4-甲氧基苯甲醇(4-MA)对血脑屏障保护作用的机制。采用线栓法制备MCAO/R模型。检测神经功能评分、脑梗死率及脑组织伊文思蓝(EB)含量。同时,测定脑组织中一氧化氮(NO)的释放及一氧化氮合酶(NOS)的活性。采用蛋白质印迹分析评估脑组织中水通道蛋白4(AQP-4)、闭合蛋白和紧密连接蛋白5的蛋白表达。用不同浓度的4-MA预处理大鼠后,神经功能评分、梗死率及脑组织中EB含量均显著降低。NO的释放以及神经元型NOS和诱导型NOS的活性均受到显著抑制。此外,AQP-4的蛋白表达明显降低,而紧密连接蛋白5和闭合蛋白的蛋白表达显著增加。综上所述,局灶性脑缺血时4-MA可降低血脑屏障的通透性。抑制NOS通路、减弱AQP-4的蛋白表达以及增强紧密连接蛋白的表达可能是4-MA对血脑屏障起保护作用的原因。