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癫痫相关基因ERG1/NSF在由海藻酸诱导的具有空间学习记忆缺陷的自发性复发性癫痫大鼠中的异常表达。

Abnormal expression of epilepsy-related gene ERG1/NSF in the spontaneous recurrent seizure rats with spatial learning memory deficits induced by kainic acid.

作者信息

Yin Shengming, Guan Zhuo, Tang Yiyuan, Zhao Jie, Hong Jaushyong, Zhang Wanqin

机构信息

Department of Physiology, Dalian Medical University, Dalian 116027, China.

出版信息

Brain Res. 2005 Aug 16;1053(1-2):195-202. doi: 10.1016/j.brainres.2005.06.054.

Abstract

Previous epilepsy-related gene screen identified a spontaneous recurrent seizure (SRS)-related gene named epilepsy-related gene (ERG1) that encodes N-ethylmaleimide-sensitive fusion protein (NSF). To explore whether spatial learning memory deficits are relevant to SRS and whether hippocampal NSF expression is altered by SRS, we used the kainic acid (KA)-induced epilepsy animal model. SRS was monitored for 3 weeks after injection of a single convulsive dose of KA. KA-treated rats with SRS, KA-treated rats without SRS, and saline-treated rats were then measured in Morris water maze. In this spatial learning task, KA-treated rats with SRS performed poorer compared to those without SRS and those treated with saline. During the subsequent probe trials, KA-treated rats with SRS spent less swim path and time in the target quadrant but more swim path and time in the opposite quadrant, and showed fewer platform crossings. Moreover, in situ hybridization and immunohistochemistry showed that both ERG1/NSF mRNA and NSF immunoreactive expression were down-regulated in the CA1 and dorsal dentate gyrus cells (dDGCs) of the hippocampus, and interestingly, tyrosine hydroxylase (TH) immunoreactive dopamine (DA) neurons were lost in ventral tegmental area (VTA) in the KA rats with SRS. These data demonstrate that SRS impairs spatial learning memory and suggest that the down-regulation of NSF expression pattern in the hippocampus and the loss of DA neurons in VTA might contribute to the spatial learning memory deficits induced by SRS.

摘要

先前的癫痫相关基因筛查鉴定出一个与自发性复发性癫痫发作(SRS)相关的基因,名为癫痫相关基因(ERG1),其编码N - 乙基马来酰亚胺敏感融合蛋白(NSF)。为了探究空间学习记忆缺陷是否与SRS相关,以及海马体中NSF表达是否因SRS而改变,我们使用了 kainic 酸(KA)诱导的癫痫动物模型。在注射单次惊厥剂量的KA后,对SRS进行了3周的监测。然后,对有SRS的KA处理大鼠、无SRS的KA处理大鼠和生理盐水处理大鼠进行了莫里斯水迷宫测试。在这个空间学习任务中,有SRS的KA处理大鼠的表现比无SRS的大鼠和生理盐水处理的大鼠更差。在随后的探索试验中,有SRS的KA处理大鼠在目标象限花费的游泳路径和时间更少,但在对侧象限花费的游泳路径和时间更多,并且平台穿越次数更少。此外,原位杂交和免疫组化显示,海马体的CA1区和背侧齿状回细胞(dDGCs)中ERG1/NSF mRNA和NSF免疫反应性表达均下调,有趣的是,在有SRS的KA大鼠中,腹侧被盖区(VTA)中酪氨酸羟化酶(TH)免疫反应性多巴胺(DA)神经元丢失。这些数据表明,SRS损害空间学习记忆,并提示海马体中NSF表达模式的下调和VTA中DA神经元的丢失可能导致SRS诱导的空间学习记忆缺陷。

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