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Chemogenetic Activation of Prefrontal Cortex in Shank3-Deficient Mice Ameliorates Social Deficits, NMDAR Hypofunction, and Sgk2 Downregulation.对Shank3基因缺陷小鼠前额叶皮层进行化学遗传学激活可改善社交缺陷、NMDAR功能减退和Sgk2下调。
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Ventral hippocampal projections to the medial prefrontal cortex regulate social memory.腹侧海马投射到内侧前额叶皮层调节社会记忆。
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Oxytocin Receptors Are Expressed by Glutamatergic Prefrontal Cortical Neurons That Selectively Modulate Social Recognition.催产素受体表达于谷氨酸能前额皮质神经元,其选择性调节社会识别。
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Temporal evolution of cortical ensembles promoting remote memory retrieval.促进远程记忆检索的皮质集合体的时间演变。
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A diverse range of factors affect the nature of neural representations underlying short-term memory.多种因素影响短期记忆的神经表象的本质。
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Engram Cell Excitability State Determines the Efficacy of Memory Retrieval.记忆印痕细胞的兴奋状态决定了记忆提取的效果。
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前额皮质神经元亚群对于社会记忆是必需的。

A Subpopulation of Prefrontal Cortical Neurons Is Required for Social Memory.

机构信息

Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania.

School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China; Department of Pharmacology, University of Virginia School of Medicine, Charlottesville, Virginia.

出版信息

Biol Psychiatry. 2021 Mar 1;89(5):521-531. doi: 10.1016/j.biopsych.2020.08.023. Epub 2020 Sep 5.

DOI:10.1016/j.biopsych.2020.08.023
PMID:33190846
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7867585/
Abstract

BACKGROUND

The medial prefrontal cortex (mPFC) is essential for social behaviors, yet whether and how it encodes social memory remains unclear.

METHODS

We combined whole-cell patch recording, morphological analysis, optogenetic/chemogenetic manipulation, and the TRAP (targeted recombination in active populations) transgenic mouse tool to study the social-associated neural populations in the mPFC.

RESULTS

Fos-TRAPed prefrontal social-associated neurons are excitatory pyramidal neurons with relatively small soma sizes and thin-tufted apical dendrite. These cells exhibit intrinsic firing features of dopamine D receptor-like neurons, show persisting firing pattern after social investigation, and project dense axons to nucleus accumbens. In behaving TRAP mice, selective inhibition of prefrontal social-associated neurons does not affect social investigation but does impair subsequent social recognition, whereas optogenetic reactivation of their projections to the nucleus accumbens enables recall of a previously encountered but "forgotten" mouse. Moreover, chemogenetic activation of mPFC-to-nucleus accumbens projections ameliorates MK-801-induced social memory impairments.

CONCLUSIONS

Our results characterize the electrophysiological and morphological features of social-associated neurons in the mPFC and indicate that these Fos-labeled, social-activated prefrontal neurons are necessary and sufficient for social memory.

摘要

背景

内侧前额叶皮质(mPFC)对于社会行为至关重要,但它是否以及如何编码社会记忆尚不清楚。

方法

我们结合全细胞膜片钳记录、形态分析、光遗传学/化学遗传学操作以及靶向重组在活跃群体中的转基因(TRAP)小鼠工具,研究 mPFC 中的与社会相关的神经群体。

结果

Fos-TRAPed 前额叶社会相关神经元是兴奋性锥体神经元,具有相对较小的胞体大小和薄树突。这些细胞表现出多巴胺 D 受体样神经元的固有放电特征,在社会调查后表现出持续的放电模式,并向伏隔核投射密集的轴突。在行为 TRAP 小鼠中,选择性抑制前额叶社会相关神经元不会影响社会调查,但会损害随后的社会识别,而光遗传学重新激活它们到伏隔核的投射则能够回忆起以前遇到但“忘记”的老鼠。此外,mPFC 到伏隔核投射的化学遗传学激活可改善 MK-801 引起的社会记忆损伤。

结论

我们的结果描述了 mPFC 中与社会相关的神经元的电生理和形态特征,并表明这些 Fos 标记的、社会激活的前额叶神经元是社会记忆所必需的。