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低频刺激通过腺苷A1受体降低点燃大鼠海马的过度兴奋性。

Low-frequency Stimulation Decreases Hyperexcitability Through Adenosine A1 Receptors in the Hippocampus of Kindled Rats.

作者信息

Shojaee Amir, Zareian Parvin, Mirnajafi-Zadeh Javad

机构信息

Department of Physiology, School of Medicine, AJA University of Medical Sciences, Tehran, Iran.

Department of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

Basic Clin Neurosci. 2020 May-Jun;11(3):333-347. doi: 10.32598/bcn.11.2.1713.1. Epub 2020 May 1.

Abstract

INTRODUCTION

In this study, the role of A1 adenosine receptors in improving the effect of Low-Frequency Electrical Stimulation (LFS) on seizure-induced hyperexcitability of hippocampal CA1 pyramidal neurons was investigated.

METHODS

A semi-rapid hippocampal kindling model was used to induce seizures in male Wistar rats. Examination of the electrophysiological properties of CA1 pyramidal neurons of the hippocampus using whole-cell patch-clamp recording 48 h after the last kindling stimulation revealed that the application of LFS as two packages of stimulations at a time interval of 6 h for two consecutive days could significantly restore the excitability CA1 pyramidal neurons evidenced by a decreased in the of the number of evoked action potentials and enhancement of amplitude, maximum rise slope and decay slope of the first evoked action potential, rheobase, utilization time, adaptation index, first-spike latency, and post-AHP amplitude. Selective locked of A1 receptors by the administration of 8-Cyclopentyl-1,3-dimethylxanthine (1 μM, 1 μl, i.c.v.) before applying each LFS package, significantly reduced LFS effectiveness in recovering these parameters.

RESULTS

On the other hand, selective activation of A1 receptors by an injection of N6-cyclohexyladenosine (10 μM, 1 μl, i.c.v.), instead of LFS application, could imitate LFS function in improving these parameters.

CONCLUSION

It is suggested that LFS exerts its efficacy on reducing the neuronal excitability, partially by activating the adenosine system and activating its A1 receptors.

摘要

引言

在本研究中,探讨了A1腺苷受体在增强低频电刺激(LFS)对癫痫诱导的海马CA1锥体神经元过度兴奋作用中的作用。

方法

采用半快速海马点燃模型诱导雄性Wistar大鼠癫痫发作。在最后一次点燃刺激后48小时,使用全细胞膜片钳记录对海马CA1锥体神经元的电生理特性进行检测,结果显示,以6小时的时间间隔连续两天将LFS作为两个刺激包应用,可显著恢复CA1锥体神经元的兴奋性,表现为诱发动作电位数量减少,首个诱发动作电位的幅度、最大上升斜率和衰减斜率增强,基强度、利用时间、适应指数、首个峰潜伏期和动作后超极化幅度降低。在每次应用LFS刺激包之前,通过注射8-环戊基-1,3-二甲基黄嘌呤(1 μM,1 μl,脑室内注射)选择性阻断A1受体,可显著降低LFS恢复这些参数的有效性。

结果

另一方面,通过注射N6-环己基腺苷(10 μM,1 μl,脑室内注射)选择性激活A1受体,而不应用LFS,可模拟LFS在改善这些参数方面的作用。

结论

提示LFS在降低神经元兴奋性方面发挥作用,部分是通过激活腺苷系统及其A1受体实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7620/7502188/9cb3626ee8f5/BCN-11-333-g001.jpg

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