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Basomedial amygdala activity in mice reflects specific and general aversion uncontrollability

Learning adaptive behaviour to control aversion is a major brain function. Detecting the absence of control is also important, although chronic uncontrollable aversion can impact maladaptively on stimulus processing in general. The mouse basomedial amygdala (BMA) contributes to aversion processing w...

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Autores principales: Ineichen, Christian, Greter, Alexandra, Baer, Mischa, Sigrist, Hannes, Sautter, Eva, Sych, Yaroslav, Helmchen, Fritjof, Pryce, Christopher R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292353/
https://www.ncbi.nlm.nih.gov/pubmed/33338290
http://dx.doi.org/10.1111/ejn.15090
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author Ineichen, Christian
Greter, Alexandra
Baer, Mischa
Sigrist, Hannes
Sautter, Eva
Sych, Yaroslav
Helmchen, Fritjof
Pryce, Christopher R.
author_facet Ineichen, Christian
Greter, Alexandra
Baer, Mischa
Sigrist, Hannes
Sautter, Eva
Sych, Yaroslav
Helmchen, Fritjof
Pryce, Christopher R.
author_sort Ineichen, Christian
collection PubMed
description Learning adaptive behaviour to control aversion is a major brain function. Detecting the absence of control is also important, although chronic uncontrollable aversion can impact maladaptively on stimulus processing in general. The mouse basomedial amygdala (BMA) contributes to aversion processing with high BMA activity associated with active behavioural responding. The overall aim of the present study was to investigate the associations between aversion (un)controllability, BMA activity and behaviour. Fibre photometry of GCaMP6‐expressing BMA neuron populations was applied in freely behaving adult male mice during exposure to mild electrical shocks, and effects of specific or general (un)controllability were investigated. In a discrete learned helplessness (LH) effect paradigm, mice underwent discrete sessions of pre‐exposure to either escapable shock (ES) or inescapable shock (IES) followed by an escape test. IES mice acquired fewer escape attempts than ES mice, and this co‐occurred with higher aversion‐related BMA activity in the IES group. After 30 days, ES and IES mice were allocated equally to either chronic social stress (CSS)—exposure to continuous uncontrollable social aversion—or control handling (CON), and on days 5 and 15 underwent an IES session. CSS mice made fewer escape attempts than CON mice, and this was now associated with lower aversion‐related BMA activity in the CSS group. These findings suggest that mouse BMA activity is higher when discrete aversion is uncontrollable but becomes lower following chronic uncontrollable aversion exposure. Therefore, BMA activity could be a neural marker of adaptive and maladaptive states consequent to specific and general uncontrollability, respectively.
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spelling pubmed-92923532022-07-20 Basomedial amygdala activity in mice reflects specific and general aversion uncontrollability Ineichen, Christian Greter, Alexandra Baer, Mischa Sigrist, Hannes Sautter, Eva Sych, Yaroslav Helmchen, Fritjof Pryce, Christopher R. Eur J Neurosci Special Issue Articles Learning adaptive behaviour to control aversion is a major brain function. Detecting the absence of control is also important, although chronic uncontrollable aversion can impact maladaptively on stimulus processing in general. The mouse basomedial amygdala (BMA) contributes to aversion processing with high BMA activity associated with active behavioural responding. The overall aim of the present study was to investigate the associations between aversion (un)controllability, BMA activity and behaviour. Fibre photometry of GCaMP6‐expressing BMA neuron populations was applied in freely behaving adult male mice during exposure to mild electrical shocks, and effects of specific or general (un)controllability were investigated. In a discrete learned helplessness (LH) effect paradigm, mice underwent discrete sessions of pre‐exposure to either escapable shock (ES) or inescapable shock (IES) followed by an escape test. IES mice acquired fewer escape attempts than ES mice, and this co‐occurred with higher aversion‐related BMA activity in the IES group. After 30 days, ES and IES mice were allocated equally to either chronic social stress (CSS)—exposure to continuous uncontrollable social aversion—or control handling (CON), and on days 5 and 15 underwent an IES session. CSS mice made fewer escape attempts than CON mice, and this was now associated with lower aversion‐related BMA activity in the CSS group. These findings suggest that mouse BMA activity is higher when discrete aversion is uncontrollable but becomes lower following chronic uncontrollable aversion exposure. Therefore, BMA activity could be a neural marker of adaptive and maladaptive states consequent to specific and general uncontrollability, respectively. John Wiley and Sons Inc. 2021-01-09 2022-05 /pmc/articles/PMC9292353/ /pubmed/33338290 http://dx.doi.org/10.1111/ejn.15090 Text en © 2020 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Issue Articles
Ineichen, Christian
Greter, Alexandra
Baer, Mischa
Sigrist, Hannes
Sautter, Eva
Sych, Yaroslav
Helmchen, Fritjof
Pryce, Christopher R.
Basomedial amygdala activity in mice reflects specific and general aversion uncontrollability
title Basomedial amygdala activity in mice reflects specific and general aversion uncontrollability
title_full Basomedial amygdala activity in mice reflects specific and general aversion uncontrollability
title_fullStr Basomedial amygdala activity in mice reflects specific and general aversion uncontrollability
title_full_unstemmed Basomedial amygdala activity in mice reflects specific and general aversion uncontrollability
title_short Basomedial amygdala activity in mice reflects specific and general aversion uncontrollability
title_sort basomedial amygdala activity in mice reflects specific and general aversion uncontrollability
topic Special Issue Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292353/
https://www.ncbi.nlm.nih.gov/pubmed/33338290
http://dx.doi.org/10.1111/ejn.15090
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