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银杏叶提取物对大鼠脑缺血/缺氧后再灌注/复氧诱导的缝隙连接变化的影响。

Effects of Gingko biloba extract on gap junction changes induced by reperfusion/reoxygenation after ischemia/hypoxia in rat brain.

作者信息

Li Zhen, Lin Xian-Ming, Gong Pei-Li, Zeng Fan-Dian, Du Guan-Hua

机构信息

Institute of Clinical Pharmacology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Am J Chin Med. 2005;33(6):923-34. doi: 10.1142/S0192415X05003430.

DOI:10.1142/S0192415X05003430
PMID:16355449
Abstract

Gap junction communication between astrocytes plays an important role in the brain. The purpose of this study was to investigate the effects of Gingko biloba extract (GBE) on the changes of connexin 43 (Cx43) mRNA and protein expression levels of rat cortex and hippocampus induced by ischemia-reperfusion and astrocyte gap junction intercellular communication (GJIC) induced by hypoxia-reoxygenation. After 2 hours of middle cerebral artery occlusion (MCAO) followed by 24 hours of reperfusion, there was obvious neurological deficit in rats. Cx43 mRNA and protein expression levels of rat cortex and hippocampus in the ischemia hemisphere were decreased significantly. When GBE at doses of 50 and 100 mg/kg body weight was administrated by p.o. daily for 7 days, the neurological deficit was improved, and lower Cx43 mRNA and protein expression levels induced by ischemia-reperfusion were recovered to normal. The i.p. injection of nimodipine (0.7 mg/kg weight body) also showed improvement on neurological deficit and Cx43 expression levels. Astrocyte GJIC was measured by the fluorescence recovery after photobleaching (FRAP). Hypoxia-reoxygenation induced a significant decrease in GJIC. Pretreatment with GBE (100 mg/l) and nimodipine (1.6 mg/l) significantly prevented the hypoxia-reoxygenation inhibition of GJIC. These results suggest that GBE could exert its neuroprotective effects by improvement of Cx43 expression and GJIC induced by hypoxia/ischemia-reoxygenation/ reperfusion injury.

摘要

星形胶质细胞之间的缝隙连接通讯在大脑中起着重要作用。本研究的目的是探讨银杏叶提取物(GBE)对缺血再灌注诱导的大鼠皮质和海马中连接蛋白43(Cx43)mRNA和蛋白表达水平变化以及缺氧复氧诱导的星形胶质细胞缝隙连接细胞间通讯(GJIC)的影响。大脑中动脉闭塞(MCAO)2小时后再灌注24小时,大鼠出现明显的神经功能缺损。缺血半球大鼠皮质和海马的Cx43 mRNA和蛋白表达水平显著降低。当以50和100mg/kg体重的剂量口服给予GBE,每日1次,持续7天时,神经功能缺损得到改善,缺血再灌注诱导的较低的Cx43 mRNA和蛋白表达水平恢复正常。腹腔注射尼莫地平(0.7mg/kg体重)也显示出神经功能缺损和Cx43表达水平的改善。通过光漂白后荧光恢复(FRAP)测量星形胶质细胞GJIC。缺氧复氧导致GJIC显著降低。用GBE(100mg/l)和尼莫地平(1.6mg/l)预处理可显著防止缺氧复氧对GJIC的抑制。这些结果表明,GBE可通过改善缺氧/缺血-复氧/再灌注损伤诱导的Cx43表达和GJIC发挥其神经保护作用。

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