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七氟醚预处理通过抗凋亡作用发挥神经保护作用。

Sevoflurane Preconditioning Confers Neuroprotection via Anti-apoptosis Effects.

作者信息

Wang Hailian, Shi Hong, Yu Qiong, Chen Jun, Zhang Feng, Gao Yanqin

机构信息

Department of Anesthesiology, Huashan Hospital, Shanghai, China.

State Key Laboratory of Medical Neurobiology, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, China.

出版信息

Acta Neurochir Suppl. 2016;121:55-61. doi: 10.1007/978-3-319-18497-5_10.

Abstract

Neuroprotection against cerebral ischemia afforded by volatile anesthetic preconditioning (APC) has been demonstrated both in vivo and in vitro, yet the underlying mechanism is poorly understood. We previously reported that repeated sevoflurane APC reduced infarct size in rats after focal ischemia. In this study, we investigated whether inhibition of apoptotic signaling cascades contributes to sevoflurane APC-induced neuroprotection. Male Sprague-Dawley rats were exposed to ambient air or 2.4 % sevoflurane for 30 min per day for 4 consecutive days and then subjected to occlusion of the middle cerebral artery (MCAO) for 60 min at 24 h after the last sevoflurane intervention. APC with sevoflurane markedly decreased apoptotic cell death in rat brains, which was accompanied by decreased caspase-3 cleavage and cytochrome c release. The apoptotic suppression was associated with increased ratios of anti-apoptotic Bcl-2 family proteins over pro-apoptotic proteins and with decreased activation of JNK and p53 pathways. Thus, our data suggest that suppression of apoptotic cell death contributes to the neuroprotection against ischemic brain injury conferred by sevoflurane preconditioning.

摘要

挥发性麻醉药预处理(APC)对脑缺血的神经保护作用已在体内和体外得到证实,但其潜在机制尚不清楚。我们之前报道过,反复七氟醚预处理可减小大鼠局灶性缺血后的梗死面积。在本研究中,我们调查了抑制凋亡信号级联反应是否有助于七氟醚预处理诱导的神经保护作用。雄性Sprague-Dawley大鼠每天暴露于空气或2.4%七氟醚中30分钟,连续4天,然后在最后一次七氟醚干预后24小时进行大脑中动脉闭塞(MCAO)60分钟。七氟醚预处理显著减少了大鼠脑中的凋亡细胞死亡,同时伴有caspase-3裂解和细胞色素c释放减少。凋亡抑制与抗凋亡Bcl-2家族蛋白与促凋亡蛋白的比例增加以及JNK和p53通路的激活减少有关。因此,我们的数据表明,抑制凋亡细胞死亡有助于七氟醚预处理对缺血性脑损伤的神经保护作用。

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