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The L-type voltage-gated calcium channel Ca(V)1.2 mediates fear extinction and modulates synaptic tone in the lateral amygdala

L-type voltage-gated calcium channels (LVGCCs) have been implicated in both the formation and the reduction of fear through Pavlovian fear conditioning and extinction. Despite the implication of LVGCCs in fear learning and extinction, studies of the individual LVGCC subtypes, Ca(V)1.2 and Ca(V)1.3,...

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Autores principales: Temme, Stephanie J., Murphy, Geoffrey G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647931/
https://www.ncbi.nlm.nih.gov/pubmed/29038219
http://dx.doi.org/10.1101/lm.045773.117
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author Temme, Stephanie J.
Murphy, Geoffrey G.
author_facet Temme, Stephanie J.
Murphy, Geoffrey G.
author_sort Temme, Stephanie J.
collection PubMed
description L-type voltage-gated calcium channels (LVGCCs) have been implicated in both the formation and the reduction of fear through Pavlovian fear conditioning and extinction. Despite the implication of LVGCCs in fear learning and extinction, studies of the individual LVGCC subtypes, Ca(V)1.2 and Ca(V)1.3, using transgenic mice have failed to find a role of either subtype in fear extinction. This discontinuity between the pharmacological studies of LVGCCs and the studies investigating individual subtype contributions could be due to the limited neuronal deletion pattern of the Ca(V)1.2 conditional knockout mice previously studied to excitatory neurons in the forebrain. To investigate the effects of deletion of Ca(V)1.2 in all neuronal populations, we generated Ca(V)1.2 conditional knockout mice using the synapsin1 promoter to drive Cre recombinase expression. Pan-neuronal deletion of Ca(V)1.2 did not alter basal anxiety or fear learning. However, pan-neuronal deletion of Ca(V)1.2 resulted in a significant deficit in extinction of contextual fear, implicating LVGCCs, specifically Ca(V)1.2, in extinction learning. Further exploration on the effects of deletion of Ca(V)1.2 on inhibitory and excitatory input onto the principle neurons of the lateral amygdala revealed a significant shift in inhibitory/excitatory balance. Together these data illustrate an important role of Ca(V)1.2 in fear extinction and the synaptic regulation of activity within the amygdala.
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spelling pubmed-56479312018-11-01 The L-type voltage-gated calcium channel Ca(V)1.2 mediates fear extinction and modulates synaptic tone in the lateral amygdala Temme, Stephanie J. Murphy, Geoffrey G. Learn Mem Research L-type voltage-gated calcium channels (LVGCCs) have been implicated in both the formation and the reduction of fear through Pavlovian fear conditioning and extinction. Despite the implication of LVGCCs in fear learning and extinction, studies of the individual LVGCC subtypes, Ca(V)1.2 and Ca(V)1.3, using transgenic mice have failed to find a role of either subtype in fear extinction. This discontinuity between the pharmacological studies of LVGCCs and the studies investigating individual subtype contributions could be due to the limited neuronal deletion pattern of the Ca(V)1.2 conditional knockout mice previously studied to excitatory neurons in the forebrain. To investigate the effects of deletion of Ca(V)1.2 in all neuronal populations, we generated Ca(V)1.2 conditional knockout mice using the synapsin1 promoter to drive Cre recombinase expression. Pan-neuronal deletion of Ca(V)1.2 did not alter basal anxiety or fear learning. However, pan-neuronal deletion of Ca(V)1.2 resulted in a significant deficit in extinction of contextual fear, implicating LVGCCs, specifically Ca(V)1.2, in extinction learning. Further exploration on the effects of deletion of Ca(V)1.2 on inhibitory and excitatory input onto the principle neurons of the lateral amygdala revealed a significant shift in inhibitory/excitatory balance. Together these data illustrate an important role of Ca(V)1.2 in fear extinction and the synaptic regulation of activity within the amygdala. Cold Spring Harbor Laboratory Press 2017-11 /pmc/articles/PMC5647931/ /pubmed/29038219 http://dx.doi.org/10.1101/lm.045773.117 Text en © 2017 Temme and Murphy; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
Temme, Stephanie J.
Murphy, Geoffrey G.
The L-type voltage-gated calcium channel Ca(V)1.2 mediates fear extinction and modulates synaptic tone in the lateral amygdala
title The L-type voltage-gated calcium channel Ca(V)1.2 mediates fear extinction and modulates synaptic tone in the lateral amygdala
title_full The L-type voltage-gated calcium channel Ca(V)1.2 mediates fear extinction and modulates synaptic tone in the lateral amygdala
title_fullStr The L-type voltage-gated calcium channel Ca(V)1.2 mediates fear extinction and modulates synaptic tone in the lateral amygdala
title_full_unstemmed The L-type voltage-gated calcium channel Ca(V)1.2 mediates fear extinction and modulates synaptic tone in the lateral amygdala
title_short The L-type voltage-gated calcium channel Ca(V)1.2 mediates fear extinction and modulates synaptic tone in the lateral amygdala
title_sort l-type voltage-gated calcium channel ca(v)1.2 mediates fear extinction and modulates synaptic tone in the lateral amygdala
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647931/
https://www.ncbi.nlm.nih.gov/pubmed/29038219
http://dx.doi.org/10.1101/lm.045773.117
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