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作 者:陈红伟[1] 洪涛[1] 叶新运[1] 宋湖平[1] 汪阳[1]
出 处:《中华神经外科杂志》2010年第5期426-429,共4页Chinese Journal of Neurosurgery
基 金:国家自然基金资助项目(30660188);江西省教育厅科学技术研究项目(GJJ10325)
摘 要:目的探讨甘珀酸对兔实验性蛛网膜下腔出血(SAH)后脑血管痉挛(CVS)时缝隙连接蛋白43(Cx43)磷酸化表达的影响。方法建立兔二次SAH模型,脑池及静脉分别给予甘珀酸,脑血管造影及光镜观察分析基底动脉直径及形态学变化并应用Western blot检测基底动脉Cx43蛋白磷酸化表达的变化。结果SAH组与正常组相比,脑血管造影及光镜观察结果证实基底动脉痉挛明显;痉挛动脉壁磷酸化的Cx43(P—Cx43)蛋白表达显著升高,但去磷酸化的Cx43(NP—Cx43)蛋白表达显著减少。甘珀酸脑池处理组及静脉处理组与SAH组相比,脑血管造影及光镜观察结果证实基底动脉痉挛显著减轻;痉挛动脉壁P—Cx43蛋白表达显著减少,但NP—Cx43蛋白表达显著升高。结论SAH后,Cx43蛋白磷酸化表达发生变化,脑池或静脉给予甘珀酸能明显缓解SAH后CVS,其作用机制可能与基底动脉Cx43蛋白磷酸化表达变化有关。Objective The study was designed to investigate the expression of Connexin43 (Cx43) phosphorylation in the basilar arteries on cerebral vasospasm after experimental subarachnoid hemorrhage(SAil) and the effects of earbenoxolone(CBX) on CVS and Cx43 phosphorylation expression in rabbits. Method The double- hemorrhage model of SAIl with injecting into the eisterna magna was used. CBX was given intraeistemally or intravenously. Angiography and hematoxylin and eosin staining were performed to observe the diameter and for morphological study of the basilar artery. Western blotting was used to analyze the phosphorylation expression of Cx43 protein in basilar artery. Results After SAH, arterial narrowing and morphological changes in vascular structure were significantly more than that in normal group. CBX inhibited these changes; compared to that in normal group, phosphorylated Cx43 was up - regulated, while dephosphorylated Cx43 was down - regulated in the basilar artery vessel wall after SAIl. CBX successfully reversed these alterations of Cx43 phosphorylation. Conclusions The expression changes of Cx43 phosphorylation plays an important role in the pathogenesis of CVS. CBX reduces cerebral vasospasm after SAH by modulating the alterations of Cx43 phosphorylation.
分 类 号:R743.35[医药卫生—神经病学与精神病学]
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