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超极化激活阳离子电流介导的可塑性改变促成了电休克诱导的抑郁大鼠学习和记忆障碍。

Alteration of hyperpolarization-activated cation current-mediated metaplasticity contributes to electroconvulsive shock-induced learning and memory impairment in depressed rats.

作者信息

Ren Li, Yu Jian, Chen Hengsheng, Luo Jie, Lv Feng, Min Su

机构信息

Department of Anesthesiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Department of Psychiatry, Shanghai 10th People's Hospital, Anesthesia and Brain Research Institute, Tongji University, Shanghai, China.

出版信息

Front Psychiatry. 2024 Jun 7;15:1365119. doi: 10.3389/fpsyt.2024.1365119. eCollection 2024.

Abstract

BACKGROUND

Accompanied by a rapid and effective antidepressant effect, electroconvulsive shock (ECS) can also induce learning and memory impairment. Our previous research reported that metaplasticity is involved in this process. However, the mechanisms still remain unclear. This study investigated the role of current in the metaplastic changes and learning and memory impairment induced by ECS in depressive rats.

METHODS

Depressive rats received ECS after modelling using chronic unpredictable. ZD7288, a type of current inhibitor was used to verify the effect of current. The sucrose preference test and Morris water maze were used for behavior testing. Changes in metaplasticity was assessed with the LTD/LTP threshold by stimulation at different frequencies. Spontaneous and evoked action potentials (APs) were measured to confirm difference of neuronal excitability. Additionally, the amplitude of current was analyzed.

RESULTS

ECS exerts antidepressant effect, but also induce spatial learning and memory dysfunction. ECS up-regulates the LTD/LTP threshold. In rats treated with ECS, the frequency of spontaneous and evoked APs is significantly reduced. In addition, ECS induces changes in the intrinsic properties of AP, including a decrease of AP-half width and peak amplitude, and an increase in AP time to peak and post-hyperpolarization potential amplitude. In particular, ECS increases both instantaneous and steady-state currents. However, Inhibition of current with ZD7288 results in a relief of learning and memory impairment and a decrease in threshold, as well as a significant reversal of whole-cell electrophysiological changes.

CONCLUSION

ECS-induced learning and memory impairment is caused by neuronal hypoexcitability mediated metaplasticity, and upregulation of LTD/LTP threshold by an increase in current.

摘要

背景

电休克(ECS)在产生快速有效的抗抑郁作用的同时,也会诱发学习和记忆障碍。我们之前的研究报道,元可塑性参与了这一过程。然而,其机制仍不清楚。本研究探讨了电流在ECS诱导的抑郁大鼠元可塑性变化及学习和记忆障碍中的作用。

方法

抑郁大鼠采用慢性不可预测应激建模后接受ECS。使用一种电流抑制剂ZD7288来验证电流的作用。采用蔗糖偏好试验和莫里斯水迷宫进行行为测试。通过不同频率刺激的长时程抑制/长时程增强(LTD/LTP)阈值评估元可塑性的变化。测量自发和诱发动作电位(APs)以确认神经元兴奋性的差异。此外,分析电流幅度。

结果

ECS发挥抗抑郁作用,但也会诱发空间学习和记忆功能障碍。ECS上调LTD/LTP阈值。在接受ECS治疗的大鼠中,自发和诱发APs的频率显著降低。此外,ECS诱导AP内在特性的变化,包括AP半宽度和峰值幅度的降低,以及AP峰值时间和超极化后电位幅度的增加。特别是,ECS增加了瞬时和稳态电流。然而,用ZD7288抑制电流可减轻学习和记忆障碍,降低阈值,并显著逆转全细胞电生理变化。

结论

ECS诱导的学习和记忆障碍是由神经元低兴奋性介导的元可塑性引起的,并且通过电流增加导致LTD/LTP阈值上调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6a/11190359/06256c2321cc/fpsyt-15-1365119-g001.jpg

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本文引用的文献

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