联想学习诱导海马 CA1 两大输入端突触电位增强,促进诱导记忆的获得

IF 5.9 2区 医学 Q1 NEUROSCIENCES
Bing-Ying Wang, Bo Wang, Bo Cao, Ling-Ling Gu, Jiayu Chen, Hua He, Zheng Zhao, Fujun Chen, Zhiru Wang
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引用次数: 0

摘要

海马突触与学习相关的功能可塑性在很大程度上仍未得到研究。在这里,我们通过一次基于奖赏的痕迹条件反射,研究了学习在背侧 CA1 海马(dCA1)中诱导的突触可塑性。局部场电位记录结合选择性光遗传抑制首先发现,在条件反射(CS)诱导的条件刺激(conditioned stimulus,CS)过程中,dCA1突触反应在通向放射层(stratum radiatum,Rad)的沙弗袢和通向黑腔(lacunosum moleculare,LMol)的颞肌输入处均有所增加。在这些 dCA1 输入端,通过在调节过程中局部阻断 NMDA 受体和全细胞记录来自天真动物的 dCA1 神经元的感觉诱发的突触反应,进一步证实了 CS 反应兴奋性突触的突触电位。在 Rad 和 LMol 中通过多点记录发现,诱导突触电位的时间过程总体上相似;这比条件行为反应出现得更晚,饱和得更早。我们的实验证明了沙弗副神经和颞神经通路诱导的与提示记忆相关的 dCA1 突触可塑性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associative Learning-Induced Synaptic Potentiation at the Two Major Hippocampal CA1 Inputs for Cued Memory Acquisition.

Learning-associated functional plasticity at hippocampal synapses remains largely unexplored. Here, in a single session of reward-based trace conditioning, we examine learning-induced synaptic plasticity in the dorsal CA1 hippocampus (dCA1). Local field-potential recording combined with selective optogenetic inhibition first revealed an increase of dCA1 synaptic responses to the conditioned stimulus (CS) induced during conditioning at both Schaffer collaterals to the stratum radiatum (Rad) and temporoammonic input to the lacunosum moleculare (LMol). At these dCA1 inputs, synaptic potentiation of CS-responding excitatory synapses was further demonstrated by locally blocking NMDA receptors during conditioning and whole-cell recording sensory-evoked synaptic responses in dCA1 neurons from naive animals. An overall similar time course of the induction of synaptic potentiation was found in the Rad and LMol by multiple-site recording; this emerged later and saturated earlier than conditioned behavioral responses. Our experiments demonstrate a cued memory-associated dCA1 synaptic plasticity induced at both Schaffer collaterals and temporoammonic pathways.

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来源期刊
Neuroscience bulletin
Neuroscience bulletin NEUROSCIENCES-
CiteScore
7.20
自引率
16.10%
发文量
163
审稿时长
6-12 weeks
期刊介绍: Neuroscience Bulletin (NB), the official journal of the Chinese Neuroscience Society, is published monthly by Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS) and Springer. NB aims to publish research advances in the field of neuroscience and promote exchange of scientific ideas within the community. The journal publishes original papers on various topics in neuroscience and focuses on potential disease implications on the nervous system. NB welcomes research contributions on molecular, cellular, or developmental neuroscience using multidisciplinary approaches and functional strategies. We feature full-length original articles, reviews, methods, letters to the editor, insights, and research highlights. As the official journal of the Chinese Neuroscience Society, which currently has more than 12,000 members in China, NB is devoted to facilitating communications between Chinese neuroscientists and their international colleagues. The journal is recognized as the most influential publication in neuroscience research in China.
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