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睫状神经营养因子可减轻局灶性脑缺血自发性高血压大鼠的空间认知障碍、皮质梗死和丘脑变性。

Ciliary neurotrophic factor attenuates spatial cognition impairment, cortical infarction and thalamic degeneration in spontaneously hypertensive rats with focal cerebral ischemia.

作者信息

Kumon Y, Sakaki S, Watanabe H, Nakano K, Ohta S, Matsuda S, Yoshimura H, Sakanaka M

机构信息

Department of Neurosurgery, Ehime University School of Medicine, Japan.

出版信息

Neurosci Lett. 1996 Mar 15;206(2-3):141-4. doi: 10.1016/s0304-3940(96)12450-2.

Abstract

Ciliary neurotrophic factor (CNTF) has been shown to exhibit potent neurotrophic activity on peripheral and central neurons in vitro and in vivo. However, it remains to be determined whether or not CNTF rescues neuronal loss due to focal cerebral ischemia and prevents ischemia-induced disability of space navigation in rats. In the present in vivo study, we infused CNTF continuously for 4 weeks into the lateral ventricle, starting just after permanent occlusion of the left middle cerebral artery (MCA) of stroke-prone spontaneous hypertensive rats. CNTF infusion prevented the occurrence of ischemia-induced learning disability in a dose-dependent manner in rats subjected to the Morris water maze task. Subsequent histological examinations showed that cortical infarction and retrograde degeneration of the ipsilateral thalamic neurons in ischemic rats infused with CNTF were significantly less severe than those in ischemic rats infused with vehicle alone. These findings suggest that postischemic CNTF treatment prevents the occurrence of spatial learning disability in rats with permanent MCA occlusion, possibly by reducing neuronal damage within the cerebral cortex and secondary retrograde degeneration of the thalamus.

摘要

睫状神经营养因子(CNTF)已被证实在体外和体内对周围神经元和中枢神经元均具有强大的神经营养活性。然而,CNTF是否能挽救局灶性脑缺血导致的神经元损失,并预防大鼠缺血诱导的空间导航功能障碍,仍有待确定。在本体内研究中,我们从易患中风的自发性高血压大鼠左大脑中动脉(MCA)永久性闭塞后立即开始,连续4周将CNTF注入侧脑室。在接受莫里斯水迷宫任务的大鼠中,注入CNTF以剂量依赖的方式预防了缺血诱导的学习功能障碍的发生。随后的组织学检查表明,注入CNTF的缺血大鼠的皮质梗死和同侧丘脑神经元的逆行性变性明显轻于仅注入赋形剂的缺血大鼠。这些发现表明,缺血后给予CNTF治疗可预防永久性MCA闭塞大鼠出现空间学习功能障碍,可能是通过减少大脑皮质内的神经元损伤和丘脑继发性逆行性变性来实现的。

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