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首页> 外文期刊>Brain research >Time dependent amelioration against ischemic brain damage by glial cell line-derived neurotrophic factor after transient middle cerebral artery occlusion in rat.
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Time dependent amelioration against ischemic brain damage by glial cell line-derived neurotrophic factor after transient middle cerebral artery occlusion in rat.

机译:大鼠短暂性大脑中动脉闭塞后,神经胶质细胞源性神经营养因子对缺血性脑损伤的时间依赖性改善。

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摘要

Time dependent influence of glial cell line-derived neurotrophic factor (GDNF) was examined after 90 min of transient middle cerebral artery occlusion (MCAO) in rats. Treatment with GDNF significantly reduced the infarct volume stained with 2,3,5-triphenyltetrazolium chloride (TTC) when GDNF was topically applied at 0 and 1 h of reperfusion, but became insignificant at 3 h as compared to vehicle group. The protective effect of GDNF was closely related to the significant reduction of the number of terminal deoxynucleotidyl transferase-mediated dUTP-biotin in situ nick end labeling (TUNEL) positive cells as well as immunofluorescently positive cells for active forms of caspases, especially active caspase-3 but not -9. Thus, the present study showed that topical application of GDNF significantly reduced infarct size in a time-dependent manner, while the therapeutic time window was shorter than other chemical compounds such as an NMDA receptor antagonist (MK-801) and a free radical scavenger (alpha-phenyl-tert-butyl-nitrone, PBN). The effect of GDNF was stronger in suppressing active caspase-3 than active caspase-9.
机译:在大鼠短暂性中脑动脉闭塞(MCAO)90分钟后,检查了神经胶质细胞系神经营养因子(GDNF)的时间依赖性影响。当在再灌注0和1小时局部应用GDNF时,用GDNF处理显着减少了2,3,5-三苯基四唑氯化物(TTC)染色的梗塞体积,但与媒介物组相比在3 h时无明显意义。 GDNF的保护作用与末端脱氧核苷酸转移酶介导的dUTP-生物素原位缺口末端标记(TUNEL)阳性细胞以及针对半胱天冬酶活性形式(尤其是活性半胱天冬酶- 3,但不是-9。因此,本研究表明,局部应用GDNF可以以时间依赖性方式显着减少梗塞面积,而治疗时间窗则短于其他化合物,例如NMDA受体拮抗剂(MK-801)和自由基清除剂( α-苯基叔丁基-硝基,PBN)。 GDNF抑制活性caspase-3的作用强于活性caspase-9。

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