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首页> 外文期刊>Brain research >Therapeutic time window of adenovirus-mediated GDNF gene transfer after transient middle cerebral artery occlusion in rat.
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Therapeutic time window of adenovirus-mediated GDNF gene transfer after transient middle cerebral artery occlusion in rat.

机译:大鼠短暂性中脑动脉闭塞后腺病毒介导的GDNF基因转移的治疗时间窗。

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摘要

The time dependent influence of adenovirus-mediated glial cell line-derived neurotrophic factor (GDNF) gene (Ad-GDNF) was examined after 90 min of transient middle cerebral artery occlusion (MCAO) in rats. Treatment with Ad-GDNF significantly reduced the infarct volume when immediately administered after the reperfusion, but became insignificant when administered at 1 h after the reperfusion as were the cases treated with vehicle- and adenoviral vector containing the E. coli lacZ gene (Ad-LacZ)-treated groups. The protective effect of GDNF was related to the significant reduction of the number of TUNEL positive cells as well as immunohistochemical positive cells for active caspase-3 but not -9. These results showed that exogenous GDNF gene transfer successfully reduced the infarct size in a time-dependant manner by suppressing active caspase-3 but not active caspase-9. However, the therapeutic time window was shorter than the effect of GDNF protein itself previously reported.
机译:在大鼠短暂性中脑动脉闭塞(MCAO)90分钟后检查了腺病毒介导的神经胶质细胞系神经营养因子(GDNF)基因(Ad-GDNF)的时间依赖性影响。再灌注后立即给予Ad-GDNF治疗可显着减少梗塞体积,但再灌注后1 h给予则无意义,如用含大肠杆菌lacZ基因的载体和腺病毒载体(Ad-LacZ )治疗组。 GDNF的保护作用与TUNEL阳性细胞和免疫组化阳性阳性细胞的数量显着减少有关,而Caspase-3却不是-9。这些结果表明,外源性GDNF基因转移通过抑制活性caspase-3而不是活性caspase-9以时间依赖的方式成功地减小了梗塞面积。然而,治疗时间窗比先前报道的GDNF蛋白本身的作用短。

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