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神经营养因子(NGF)在局灶性脑缺血后给予时的神经保护作用的治疗时间窗。

Therapeutic time window for the neuroprotective effects of NGF when administered after focal cerebral ischemia.

机构信息

Department of Medical Imaging, The Second Hospital of Hebei Medical University, 215 West Heping Road, Shijiazhuang, 050000 Hebei Province, China.

出版信息

Neurol Sci. 2011 Jun;32(3):433-41. doi: 10.1007/s10072-011-0512-9. Epub 2011 Mar 16.

Abstract

In the present study, we evaluated the neuroprotection time window for nerve growth factor (NGF) after ischemia/reperfusion brain injury in rabbits as related to this anti-apoptosis mechanism. Male New Zealand rabbits were subjected to 2 h of middle cerebral artery occlusion (MCAO), followed by 70 h of reperfusion. NGF was administered after injury to evaluate the time window. Neurological deficits, infarct volume, neural cell apoptosis and expressions of caspase-3 and Bcl-2 were measured. Compared to saline-treated control, NGF treatment at 2, 3 and 5 h after MCAO significantly reduced infarct volume, neural cell apoptosis and expression of caspase-3 (P < 0.01), up-regulated the expression of Bcl-2 and improved functional recovery (P < 0.01). However, treatment at latter time points did not produce significant neuroprotection. Neuroprotection treatment with NGF provides an extended time window of up to 5 h after ischemia/reperfusion brain injury, in part by attenuating the apoptosis.

摘要

在本研究中,我们评估了神经生长因子(NGF)在兔脑缺血再灌注损伤后的神经保护时间窗,这与这种抗细胞凋亡机制有关。雄性新西兰兔接受 2 小时大脑中动脉闭塞(MCAO),然后再灌注 70 小时。在损伤后给予 NGF 以评估时间窗。测量神经功能缺损、梗死体积、神经细胞凋亡以及 caspase-3 和 Bcl-2 的表达。与盐水处理的对照组相比,MCAO 后 2、3 和 5 小时给予 NGF 治疗可显著降低梗死体积、神经细胞凋亡和 caspase-3 的表达(P < 0.01),上调 Bcl-2 的表达并改善功能恢复(P < 0.01)。然而,在较晚的时间点治疗并没有产生显著的神经保护作用。NGF 的神经保护治疗提供了长达缺血再灌注脑损伤后 5 小时的延长时间窗,部分是通过减轻细胞凋亡。

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