Department of Medical Imaging, The Second Hospital of Hebei Medical University, 215 West Heping Road, Shijiazhuang, 050000 Hebei Province, China.
Neurol Sci. 2011 Jun;32(3):433-41. doi: 10.1007/s10072-011-0512-9. Epub 2011 Mar 16.
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.
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。