Septal cholinergic input to CA2 hippocampal region controls social novelty discrimination via nicotinic receptor-mediated disinhibition

Author:

Pimpinella Domenico1,Mastrorilli Valentina2,Giorgi Corinna13,Coemans Silke1,Lecca Salvatore4ORCID,Lalive Arnaud L4,Ostermann Hannah5,Fuchs Elke C5,Monyer Hannah5,Mele Andrea2ORCID,Cherubini Enrico1,Griguoli Marilena16ORCID

Affiliation:

1. European Brain Research Institute (EBRI), Fondazione Rita Levi-Montalcini

2. Department of Biology and Biotechnology ‘C. Darwin’, Center for Research in Neurobiology ‘D. Bovet’, Sapienza University of Rome

3. Institute of Molecular Biology and Pathology of the National Council of Research (IBPM-CNR)

4. Department of Fundamental Neurosciences, University of Lausanne

5. Department of Clinical Neurobiology of the Medical Faculty of Heidelberg University and German Cancer Research Center (DKFZ)

6. Institute of Neuroscience of the National Research Council (IN-CNR)

Abstract

Acetylcholine (ACh), released in the hippocampus from fibers originating in the medial septum/diagonal band of Broca (MSDB) complex, is crucial for learning and memory. The CA2 region of the hippocampus has received increasing attention in the context of social memory. However, the contribution of ACh to this process remains unclear. Here, we show that in mice, ACh controls social memory. Specifically, MSDB cholinergic neurons inhibition impairs social novelty discrimination, meaning the propensity of a mouse to interact with a novel rather than a familiar conspecific. This effect is mimicked by a selective antagonist of nicotinic AChRs delivered in CA2. Ex vivo recordings from hippocampal slices provide insight into the underlying mechanism, as activation of nAChRs by nicotine increases the excitatory drive to CA2 principal cells via disinhibition. In line with this observation, optogenetic activation of cholinergic neurons in MSDB increases the firing of CA2 principal cells in vivo. These results point to nAChRs as essential players in social novelty discrimination by controlling inhibition in the CA2 region.

Funder

Fondazione Telethon

Fondazione Umberto Veronesi

Fondazione Sovena

Horizon 2020 - Research and Innovation Framework Programme

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3