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Comparison of inbred mouse substrains reveals segregation of maladaptive fear phenotypes

Maladaptive fear, such as fear that is persistent or easily generalized to a nonthreatening stimuli, is associated with anxiety-related disorders in humans. In the laboratory, maladaptive fear can be modeled in rodents using Pavlovian fear conditioning. Recently, an inbred mouse strain known as 129S...

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Autores principales: Temme, Stephanie J., Bell, Ryan Z., Pahumi, Reciton, Murphy, Geoffrey G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139001/
https://www.ncbi.nlm.nih.gov/pubmed/25191238
http://dx.doi.org/10.3389/fnbeh.2014.00282
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author Temme, Stephanie J.
Bell, Ryan Z.
Pahumi, Reciton
Murphy, Geoffrey G.
author_facet Temme, Stephanie J.
Bell, Ryan Z.
Pahumi, Reciton
Murphy, Geoffrey G.
author_sort Temme, Stephanie J.
collection PubMed
description Maladaptive fear, such as fear that is persistent or easily generalized to a nonthreatening stimuli, is associated with anxiety-related disorders in humans. In the laboratory, maladaptive fear can be modeled in rodents using Pavlovian fear conditioning. Recently, an inbred mouse strain known as 129S1/SvImJ, or 129S1 has been reported as exhibiting impairments in fear extinction and enhanced fear generalization. With a long-term goal of identifying segregating genetic markers of maladaptive fear, we used Pavlovian fear conditioning to characterize a closely related substrain designated as 129S6/SvEvTac, or 129S6. Here we report that, like 129S1 animals, 129S6 mice exhibit appropriate levels of fear upon conditioning, but are unable to extinguish fear memories once they are consolidated. Importantly, the maladaptive fear phenotype in this inbred stain can be segregated by sub-strain when probed using conditioning protocols designed to assess generalized fear. We find that unlike the 129S1 substrain, mice from the 129S6 sub-strain do not generalize conditioned fear to previously novel contexts and can learn to discriminate between two similar contexts when trained using a discrimination protocol. These results suggest that at least two forms of maladaptive fear (deficits in fear extinction and fear generalization) can be can be functionally segregated, further suggesting that the underlying neurobiology is heritable. Given the observation that two closely related sub-strains can exhibit different constellations of maladaptive fear suggests that these findings could be exploited to facilitate the identification of candidate genes for anxiety-related disorders.
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spelling pubmed-41390012014-09-04 Comparison of inbred mouse substrains reveals segregation of maladaptive fear phenotypes Temme, Stephanie J. Bell, Ryan Z. Pahumi, Reciton Murphy, Geoffrey G. Front Behav Neurosci Neuroscience Maladaptive fear, such as fear that is persistent or easily generalized to a nonthreatening stimuli, is associated with anxiety-related disorders in humans. In the laboratory, maladaptive fear can be modeled in rodents using Pavlovian fear conditioning. Recently, an inbred mouse strain known as 129S1/SvImJ, or 129S1 has been reported as exhibiting impairments in fear extinction and enhanced fear generalization. With a long-term goal of identifying segregating genetic markers of maladaptive fear, we used Pavlovian fear conditioning to characterize a closely related substrain designated as 129S6/SvEvTac, or 129S6. Here we report that, like 129S1 animals, 129S6 mice exhibit appropriate levels of fear upon conditioning, but are unable to extinguish fear memories once they are consolidated. Importantly, the maladaptive fear phenotype in this inbred stain can be segregated by sub-strain when probed using conditioning protocols designed to assess generalized fear. We find that unlike the 129S1 substrain, mice from the 129S6 sub-strain do not generalize conditioned fear to previously novel contexts and can learn to discriminate between two similar contexts when trained using a discrimination protocol. These results suggest that at least two forms of maladaptive fear (deficits in fear extinction and fear generalization) can be can be functionally segregated, further suggesting that the underlying neurobiology is heritable. Given the observation that two closely related sub-strains can exhibit different constellations of maladaptive fear suggests that these findings could be exploited to facilitate the identification of candidate genes for anxiety-related disorders. Frontiers Media S.A. 2014-08-20 /pmc/articles/PMC4139001/ /pubmed/25191238 http://dx.doi.org/10.3389/fnbeh.2014.00282 Text en Copyright © 2014 Temme, Bell, Pahumi and Murphy. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Temme, Stephanie J.
Bell, Ryan Z.
Pahumi, Reciton
Murphy, Geoffrey G.
Comparison of inbred mouse substrains reveals segregation of maladaptive fear phenotypes
title Comparison of inbred mouse substrains reveals segregation of maladaptive fear phenotypes
title_full Comparison of inbred mouse substrains reveals segregation of maladaptive fear phenotypes
title_fullStr Comparison of inbred mouse substrains reveals segregation of maladaptive fear phenotypes
title_full_unstemmed Comparison of inbred mouse substrains reveals segregation of maladaptive fear phenotypes
title_short Comparison of inbred mouse substrains reveals segregation of maladaptive fear phenotypes
title_sort comparison of inbred mouse substrains reveals segregation of maladaptive fear phenotypes
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139001/
https://www.ncbi.nlm.nih.gov/pubmed/25191238
http://dx.doi.org/10.3389/fnbeh.2014.00282
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