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作 者:孙琳[1] 刘爱芬[2] 李义召[2] 陈立云[2] 王晓云[1] 韩恩吉[2]
机构地区:[1]山东大学第二医院神经内科,山东济南250033 [2]山东大学齐鲁医院神经内科,山东济南250033
出 处:《中国病理生理杂志》2005年第12期2427-2430,共4页Chinese Journal of Pathophysiology
基 金:山东省科委资助项目(NO.973000056)
摘 要:目的:研究银杏叶制剂对大鼠脑缺血再灌注后热休克蛋白(HSP)、C-FOS表达的影响,探讨其神经保护机制。方法:采用改良LONGA法复制大鼠局灶脑缺血再灌注模型。56只实验大鼠随机分为正常对照组、假手术组、缺血再灌注组及银杏叶制剂预处理组。银杏组大鼠在实验前灌服银杏制剂2 ML,1日3次,连用5 D。应用HSP70及 C-FOS免疫组化染色、C-FOS MRNA原位杂交、原位细胞凋亡及HE染色等方法观察缺血再灌注不同时点(1 H、6 H、12 H、24 H、3 D、7 D)两者的变化,并对其阳性结果进行半定量分析。结果:银杏制剂预处理组各时段神经细胞缺血程度明显轻于未处理组、TUNEL阳性细胞数明显少于未处理组,HSP70及C-FOS表达的阳性细胞数则明显多于未处理组 (P<0.01)。脑缺血再灌注组1 H时C-FOS即有表达,6 H达高峰,后逐渐下降。再灌注6 H组HSPT0在缺血侧皮质及基底节开始表达,24 H达高峰。再灌注6 H细胞凋亡最显著。结论:银杏制剂可能通过诱导HSP70及C-FOS的表达, 发挥其神经保护作用。AIM: To investigate the influence of Ginkgo biloba extract (GBE) on the expression of c - fos, heat shock protein 70 (HSP70) during focal cerebral ischemic reperfusion in rots. METHODS: The middle cerebral artery occlusion (MCAO) model described by Zea longa was used. Healthy Wistar rots were randomized to 4 groups. Immunohistochemistry, in situ hybridization and terminal deoxynucleotidyl transferase - mediated dUTP nick end labeling (TUNEL) were used to detect the expression of c - fos gene, HSP70 and cell apoptosis at different reperfusion time points: 1, 6, 12, 24 hours and 3, 7 days after recirculation. RESULTS: The positive reactions of both c - los and HSP70 were significantly increased at different reperfusion time in GBE - pretreated ischemia/reperfusion (IR) group than those in ischemia/reperfusion group ( P 〈 0.01 ) and the number of TUNEL - positive cells was reduced in GBE - pretreated IR group. CONCLUSION: The GBE induced the expression of c - fos, HSP70 and contributes to neuroprotective activities after cerebral ischemia.
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