[束缚应激通过激活 Rho/ROCK 信号通路诱导大鼠杏仁核血脑屏障损伤]。

G Xu, A Gao, B Cong
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引用次数: 0

摘要

目的研究Rho/ROCK信号通路在介导束缚应激诱导的大鼠杏仁核血脑屏障(BBB)损伤中的作用:将60只雄性SD大鼠随机平均分为对照组(每天断食断水6小时)、束缚应激组(每天束缚6小时)、应激+法舒地尔治疗组(束缚6小时前30分钟腹腔注射1 mg/100 g)和单独法舒地尔治疗组。采用高架迷宫试验检测大鼠的行为变化,用酶联免疫吸附法测定血清皮质酮和S100B水平,并检测脑组织中伊文思蓝渗漏以评估BBB通透性的变化。用免疫荧光检测法和 Western 印迹法检测杏仁核中紧密连接蛋白表达水平的变化,用 Pull-down 试验和 Western 印迹法检测 Rho/ROCK 通路的激活情况。透射电子显微镜观察脑微血管内皮细胞的超微结构变化:结果:与对照组相比,束缚应激组和应激+法舒地尔组大鼠表现出明显的焦虑样行为,血清皮质酮水平显著升高(PPP结论:束缚应激和应激+法舒地尔组大鼠均表现出明显的焦虑样行为,血清皮质酮水平显著升高(PPP):束缚应激通过激活 Rho/ROCK 信号通路诱导大鼠杏仁核 BBB 损伤。
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[Restraint stress induces blood-brain barrier injury in rat amygdala by activating the Rho/ROCK signaling pathway].

Objective: To investigate the role of Rho/ROCK signaling pathway in mediating restraint stress-induced blood-brain barrier (BBB) injury in the amygdala of rats.

Methods: Sixty male SD rats were randomized equally into control group (with food and water deprivation for 6 h per day), restraint stress group (with restraint for 6 h per day), stress + fasudil treatment (administered by intraperitoneal injection at 1 mg/100 g 30 min before the 6-h restraint) group, and fasudil treatment alone group. The elevated plus-maze test was used to detect behavioral changes of the rats, serum corticosterone and S100B levels were determined with ELISA, and Evans Blue leakage in the brain tissue was examined to evaluate the changes in BBB permeability. The changes in expression levels of tight junction proteins in the amygdala were detected using immunofluorescence assay and Western blotting, and Rho/ROCK pathway activation was detected by Pull-down test and Western blotting. Ultrastructural changes of the cerebral microvascular endothelial cells were observed using transmission electron microscopy.

Results: Compared with those in the control group, the rats in restrain stress group and stress+fasudil group showed obvious anxiety-like behavior with significantly increased serum corticosterone level (P<0.001). Compared with those in the control group and stress+fasudil group, the rat models of restrain stress showed more obvious Evans Blue leakage and higher S100B expression (P<0.01) but lower expressions of tight junction proteins in the amygdala. Pull-down test and Western blotting confirmed that the expression levels of RhoA-GTP, ROCK2 and P-MLC 2 were significantly higher in stress group than in the control group and stress + fasudil group (P<0.05). Transmission electron microscopy revealed obvious ultrastructural changes in the cerebral microvascular endothelial cells in the rat models of restrain stress.

Conclusion: Restraint stress induces BBB injury in the amygdala of rats by activating the Rho/ROCK signaling pathway.

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208
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