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作 者:周丽华[1] 李方澜[1] 袁群芳[1] 姚志彬[1]
机构地区:[1]中山大学中山医学院人体解剖学教研室,广州市510080
出 处:《中华显微外科杂志》2003年第3期204-206,共3页Chinese Journal of Microsurgery
基 金:广东省科委社会发展攻关项目 (2 0 0 2C30 1 1 1 )
摘 要:目的 比较植物抗氧化剂TA90 0 1和EGb761对臂丛根性撕脱后C7前角运动神经元c jun、nNOS表达和运动神经元存活的影响。 方法 成年Sprague Dawley雌性大鼠 180只 ,随机分为TA90 0 1组、EG761组和对照组。行右侧臂丛神经根性撕脱术后 ,三组大鼠每天分别给予腹腔注射 1ml0 5 %TA90 0 1、0 5 %EGb761和生理盐水。治疗后 4h、12h、1d、3d、5d、1周、2周、4周和 6周取材 ,行c jun免疫细胞化学、NADPH d组织化学和中性红复染。 结果 c jun和nNOS仅在损伤运动神经元出现 ,c jun表达开始于 4h ,1d达高峰 ,随后下降直至 2周。nNOS表达从 5d开始 ,2周达高峰 ,以后逐渐下降至 6周。运动神经元的死亡开始于 2周 ,以 4周~ 6周最明显。TA90 0 1和EGb761治疗后都能上调c jun ,下调nNOS表达 ,提高运动神经元存活。EGb761上调c jun表达的程度明显强于TA990 1;两者减少NOS表达和提高运动神经元存活的效果一致。 结论 TA990 1和EGb761都有保护受损运动神经元的功效 ,nNOS表达与运动神经元死亡的关系更密切。Objective To compare the effect of natural antioxidants TA9001 and EGb761 on c-jun, NOS expression and survival of spinal motoneurons following brachial roots avulsion. Methods One hundred and eighty adult Sprague-Dawley female rats were randomly divided into TA9001, ECb761 and control groups. The right C 5~T 1 nerve roots were avulsed and then the introperitoneal injection of 1ml of 0.5% TA9001, 0.5% EGb761 or normal saline was given immediately and once daily to the rats, respectively. The rats were killed after survival for 4 h, 12 h 1 d,3 d,5 d,and 1 week, 2 weeks, 4 weeks and 6 weeks. The cryostat sections of C 7 segment were prepared and carried with c-jun immunocytochemistry, NADPH-d histochemistry and neutral red counter stain. Results The c-jun and nNOS gene expression was only appeared in injured motoneurons. c-jun was first appeared at 4 h, reached its maximum at 1 d, and grandually decreased till 2 weeks. NOS was first checked at 5 d, mostly at 2 weeks and decreased until 6 weeks. Avulsed motoneuron death started at 2 weeks, reached its peak at 4~6 weeks. Both TA9001 and EGb761 can cause c-jun up-regulation, nNOS down-regulation and more motoneuron survival as compared to control. Furthermore, EGb761 had more power to enhance c-jun expression than TA9901 at each time point. Conclusion It seems that nNOS is more important in motoneuron death mechanism than c-jun. Treatment of either TA9901 or EGb761 can protect the injured motoneurons following root avulsion.
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