[Effects of post-traumatic stress disorder on the excitability of glutamatergic and GABAergic neurons in dorsal and ventral hippocampus in mice].

Q3 Medicine Acta physiologica Sinica Pub Date : 2023-06-25
Dong-Bo Liu, Yan Shi, Shen-Ping Zheng, Hao-Ran Zhou, Li-Wei Zhao
{"title":"[Effects of post-traumatic stress disorder on the excitability of glutamatergic and GABAergic neurons in dorsal and ventral hippocampus in mice].","authors":"Dong-Bo Liu,&nbsp;Yan Shi,&nbsp;Shen-Ping Zheng,&nbsp;Hao-Ran Zhou,&nbsp;Li-Wei Zhao","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The purpose of this study was to investigate the effects of post-traumatic stress disorder (PTSD) on electrophysiological characteristics of glutamatergic and GABAergic neurons in dorsal hippocampus (dHPC) and ventral hippocampus (vHPC) in mice, and to elucidate the mechanisms underlying the plasticity of hippocampal neurons and memory regulation after PTSD. Male C57Thy1-YFP/GAD67-GFP mice were randomly divided into PTSD group and control group. Unavoidable foot shock (FS) was applied to establish PTSD model. The spatial learning ability was explored by water maze test, and the changes in electrophysiological characteristics of glutamatergic and GABAergic neurons in dHPC and vHPC were examined using whole-cell recording method. The results showed that FS significantly reduced the movement speed, and enhanced the number and percentage of freezing. PTSD significantly prolonged the escape latency in localization avoidance training, shortened the swimming time in the original quadrant, extended the swimming time in the contralateral quadrant, and increased absolute refractory period, energy barrier and inter-spike interval of glutamatergic neurons in dHPC and GABAergic neurons in vHPC, while decreased absolute refractory period, energy barrier and inter-spike interval of GABAergic neurons in dHPC and glutamatergic neurons in vHPC. These results suggest that PTSD can damage spatial perception of mice, down-regulate the excitability of dHPC and up-regulate the excitability of vHPC, and the underlying mechanism may involve the regulation of spatial memory by the plasticity of neurons in dHPC and vHPC.</p>","PeriodicalId":7134,"journal":{"name":"Acta physiologica Sinica","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta physiologica Sinica","FirstCategoryId":"1087","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

The purpose of this study was to investigate the effects of post-traumatic stress disorder (PTSD) on electrophysiological characteristics of glutamatergic and GABAergic neurons in dorsal hippocampus (dHPC) and ventral hippocampus (vHPC) in mice, and to elucidate the mechanisms underlying the plasticity of hippocampal neurons and memory regulation after PTSD. Male C57Thy1-YFP/GAD67-GFP mice were randomly divided into PTSD group and control group. Unavoidable foot shock (FS) was applied to establish PTSD model. The spatial learning ability was explored by water maze test, and the changes in electrophysiological characteristics of glutamatergic and GABAergic neurons in dHPC and vHPC were examined using whole-cell recording method. The results showed that FS significantly reduced the movement speed, and enhanced the number and percentage of freezing. PTSD significantly prolonged the escape latency in localization avoidance training, shortened the swimming time in the original quadrant, extended the swimming time in the contralateral quadrant, and increased absolute refractory period, energy barrier and inter-spike interval of glutamatergic neurons in dHPC and GABAergic neurons in vHPC, while decreased absolute refractory period, energy barrier and inter-spike interval of GABAergic neurons in dHPC and glutamatergic neurons in vHPC. These results suggest that PTSD can damage spatial perception of mice, down-regulate the excitability of dHPC and up-regulate the excitability of vHPC, and the underlying mechanism may involve the regulation of spatial memory by the plasticity of neurons in dHPC and vHPC.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[创伤后应激障碍对小鼠海马背侧和腹侧谷氨酸能和gaba能神经元兴奋性的影响]。
本研究旨在探讨创伤后应激障碍(PTSD)对小鼠背侧海马(dHPC)和腹侧海马(vHPC)谷氨酸能神经元和gaba能神经元电生理特性的影响,并探讨PTSD后海马神经元可塑性和记忆调节的机制。雄性C57Thy1-YFP/GAD67-GFP小鼠随机分为PTSD组和对照组。采用不可避免足部冲击(FS)建立创伤后应激障碍模型。采用水迷宫实验探索大鼠空间学习能力,采用全细胞记录法检测大鼠dHPC和vHPC中谷氨酸能神经元和gaba能神经元电生理特性的变化。结果表明,FS显著降低了运动速度,增加了冻结次数和百分比。PTSD显著延长了定位回避训练的逃避潜伏期,缩短了原象限游泳时间,延长了对侧象限游泳时间,增加了dHPC中谷氨酸能神经元和vHPC中gaba能神经元的绝对不应期、能量屏障和峰间间隔,减少了dHPC中gaba能神经元和vHPC中谷氨酸能神经元的绝对不应期、能量屏障和峰间间隔。上述结果提示,创伤后应激障碍可损伤小鼠的空间知觉,下调dHPC的兴奋性,上调vHPC的兴奋性,其机制可能与dHPC和vHPC神经元的可塑性对空间记忆的调节有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Acta physiologica Sinica
Acta physiologica Sinica Medicine-Medicine (all)
CiteScore
1.20
自引率
0.00%
发文量
4820
期刊介绍: Acta Physiologica Sinica (APS) is sponsored by the Chinese Association for Physiological Sciences and Shanghai Institutes of Biological Sciences, Chinese Academy of Sciences (CAS), and is published bimonthly by the Science Press, China. APS publishes original research articles in the field of physiology as well as research contributions from other biomedical disciplines and proceedings of conferences and symposia of physiological sciences. Besides “Original Research Articles”, the journal also provides columns as “Brief Review”, “Rapid Communication”, “Experimental Technique”, and “Letter to the Editor”. Articles are published in either Chinese or English according to authors’ submission.
期刊最新文献
[Baduanjin improves sleep quality in patients with type 2 diabetes possibly via regulating Bmal1 gene]. [Construction of a mouse model of type 2 diabetes induced by high fat diet alone and evaluation of pathological changes]. [Effect of metabolic reprogramming on abdominal aortic aneurysm]. [Effects of different exercise modes on neuromuscular junction and metabolism of skeletal muscle-related proteins in aging rats]. [Noise exposure-induced stress response and its measurement methods].
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1