首页> 外文期刊>Acta Cirurgica Brasileira >Efficacy of phosphocreatine pre-administration on XIAP and Smac in ischemic penumbra of rats with focal cerebral ischemia reperfusion injury 1
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Efficacy of phosphocreatine pre-administration on XIAP and Smac in ischemic penumbra of rats with focal cerebral ischemia reperfusion injury 1

机译:磷酸肌酸对局灶性脑缺血再灌注大鼠缺血半影中XIAP和Smac的作用1

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Purpose: To observe the efficacy of phosphocreatine pre-administration (PCr-PA) on X-linked inhibitor of apoptosis protein (XIAP), the second mitochondia-derived activator of caspase (Smac) and apoptosis in the ischemic penumbra of rats with focal cerebral ischemia-reperfusion injury (CIRI). Methods: A total of 60 healthy male Sprague Dawley (SD) rats were randomly divided into three groups (n=20): group A (the sham operation group), group B intraperitoneally injected with 20 mg/kg (10 mg/ml) of saline before preparing the ischemia-reperfusion (IR) model, and group C intraperitoneally injected with 20 mg/kg (10 mg/ml) of PCr immediately before preparing the IR model. After 24 h for reperfusion, the neurological function was evaluated and the tissue was sampled to detect expression of XIAP, Smac and caspase-3 positive cells in the ischemic penumbra so as to observe the apoptosis. Results: Compared with group B, neurological deficit scores, numbers of apoptotic cells, expression of Smac,caspase-9 and the numbers of Caspase-3 positive cells were decreased while expression of XIAP were increased in the ischemic penumbra of group C. Conclusions: Phosphocreatine pre-administration may elicit neuroprotective effects in the brain by increasing expression of X-linked inhibitor of apoptosis protein, reducing expression of second mitochondia-derived activator of caspase, and inhibiting the apoptosis in the ischemic penumbra.
机译:目的:观察磷酸肌酸预给药(PCr-PA)对X连锁凋亡蛋白(XIAP),线粒体第二种半胱天冬酶(Smac)激活剂和局部脑缺血半影区细胞凋亡的影响。缺血再灌注损伤(CIRI)。方法:将60只健康的雄性Sprague Dawley(SD)雄性大鼠随机分为三组(n = 20):A组(假手术组),B组<腹膜内注射20 mg / kg(10 mg / ml) )在准备缺血再灌注(IR)模型之前先用生理盐水冲洗),然后将C组<立即在准备IR模型之前腹膜内注射20 mg / kg(10 mg / ml)PCr>。再灌注24小时后,评估神经功能并取样组织以检测缺血半影中XIAP,Smac和caspase-3阳性细胞的表达,从而观察其凋亡。结果:与B组相比,C组缺血性半影​​的神经功能缺损评分,凋亡细胞数量,Smac,caspase-9表达和Caspase-3阳性细胞数量减少,而XIAP的表达增加。磷酸肌酸的预给药可通过增加X连锁的凋亡蛋白抑制剂的表达,减少第二个线粒体衍生的caspase激活剂的表达并抑制缺血半影中的凋亡来在大脑中引起神经保护作用。

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