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基于NHE-1/钙蛋白酶1通路下调NHE-1可减少癫痫模型大鼠海马细胞的凋亡。

Downregulating NHE-1 decreases the apoptosis of hippocampal cells in epileptic model rats based on the NHE-1/calpain1 pathway.

作者信息

Peng Shuang, Wu Xuling, Zheng Qian, Xu Jianwei, Xie Dongjun, Zhou Mengyun, Wang Mingwei, Cheng Yongran, Ye Lan, Mo Xiangang, Feng Zhanhui

机构信息

Department of Neurology, The Affiliated Hospital of Guizhou Medical University. Guiyang, China.

Center for Tissue Engineering and Stem Cell Research, School of Basic Medicine,Guizhou Medical University, Guiyang, China.

出版信息

Heliyon. 2023 Jul 15;9(7):e18336. doi: 10.1016/j.heliyon.2023.e18336. eCollection 2023 Jul.

Abstract

Seizure is associated with pathological changes of hippocampus, but the mechanism by which hippocampal neuronal apoptosis promotes epilepsy is unclear. Our previous study showed that the expression of NHE-1 was increased in epileptic model rats. Therefore, this study further explores the effect of NHE-1 on hippocampal cells apoptosis and seizure in lithium chloride-pilocarpine epileptic model rats. First, we established a lithium chloride-pilocarpine induced epileptic rat model and detected the expression of NHE-1, calpain1 and apoptosis in the hippocampus. Then, we further down-regulated NHE-1 to observe the expression of calpain1 and apoptosis in the hippocampus, as well as its effect on seizures in rats. We found that the expression of NHE-1 and calpain1 and apoptosis in the hippocampus was significant increased in the model group. After down-regulating NHE-1, the expression of calpain1 was decreased, and hippocampal cell apoptosis was alleviated. In addition, down-regulation of NHE-1 reduced the frequency and duration of seizures in epileptic rats. Therefore, hippocampal NHE-1 overexpression is closely related to the development of neuronal apoptosis in a rat model of epilepsy, and downregulating NHE-1 expression can reduce cell apoptosis. Moreover, the NHE-1/calpain1 signaling pathway may be an important mechanism leading to hippocampal cell apoptosis.

摘要

癫痫发作与海马体的病理变化相关,但海马体神经元凋亡促进癫痫的机制尚不清楚。我们之前的研究表明,癫痫模型大鼠中NHE-1的表达增加。因此,本研究进一步探讨NHE-1对氯化锂-匹罗卡品癫痫模型大鼠海马体细胞凋亡和癫痫发作的影响。首先,我们建立了氯化锂-匹罗卡品诱导的癫痫大鼠模型,并检测海马体中NHE-1、钙蛋白酶1的表达及细胞凋亡情况。然后,我们进一步下调NHE-1,以观察海马体中钙蛋白酶1的表达、细胞凋亡情况及其对大鼠癫痫发作的影响。我们发现,模型组海马体中NHE-1、钙蛋白酶1的表达及细胞凋亡显著增加。下调NHE-1后,钙蛋白酶1的表达降低,海马体细胞凋亡得到缓解。此外,下调NHE-1可降低癫痫大鼠的癫痫发作频率和持续时间。因此,海马体NHE-1过表达与癫痫大鼠模型中神经元凋亡的发生密切相关,下调NHE-1表达可减少细胞凋亡。此外,NHE-1/钙蛋白酶1信号通路可能是导致海马体细胞凋亡的重要机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b22c/10395532/045f963e535b/gr1.jpg

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