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Transient acidosis while retrieving a fear-related memory enhances its lability

Attenuating the strength of fearful memories could benefit people disabled by memories of past trauma. Pavlovian conditioning experiments indicate that a retrieval cue can return a conditioned aversive memory to a labile state. However, means to enhance retrieval and render a memory more labile are...

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Autores principales: Du, Jianyang, Price, Margaret P, Taugher, Rebecca J, Grigsby, Daniel, Ash, Jamison J, Stark, Austin C, Hossain Saad, Md Zubayer, Singh, Kritika, Mandal, Juthika, Wemmie, John A, Welsh, Michael J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484615/
https://www.ncbi.nlm.nih.gov/pubmed/28650315
http://dx.doi.org/10.7554/eLife.22564
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author Du, Jianyang
Price, Margaret P
Taugher, Rebecca J
Grigsby, Daniel
Ash, Jamison J
Stark, Austin C
Hossain Saad, Md Zubayer
Singh, Kritika
Mandal, Juthika
Wemmie, John A
Welsh, Michael J
author_facet Du, Jianyang
Price, Margaret P
Taugher, Rebecca J
Grigsby, Daniel
Ash, Jamison J
Stark, Austin C
Hossain Saad, Md Zubayer
Singh, Kritika
Mandal, Juthika
Wemmie, John A
Welsh, Michael J
author_sort Du, Jianyang
collection PubMed
description Attenuating the strength of fearful memories could benefit people disabled by memories of past trauma. Pavlovian conditioning experiments indicate that a retrieval cue can return a conditioned aversive memory to a labile state. However, means to enhance retrieval and render a memory more labile are unknown. We hypothesized that augmenting synaptic signaling during retrieval would increase memory lability. To enhance synaptic transmission, mice inhaled CO(2) to induce an acidosis and activate acid sensing ion channels. Transient acidification increased the retrieval-induced lability of an aversive memory. The labile memory could then be weakened by an extinction protocol or strengthened by reconditioning. Coupling CO(2) inhalation to retrieval increased activation of amygdala neurons bearing the memory trace and increased the synaptic exchange from Ca(2+)-impermeable to Ca(2+)-permeable AMPA receptors. The results suggest that transient acidosis during retrieval renders the memory of an aversive event more labile and suggest a strategy to modify debilitating memories. DOI: http://dx.doi.org/10.7554/eLife.22564.001
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spelling pubmed-54846152017-07-18 Transient acidosis while retrieving a fear-related memory enhances its lability Du, Jianyang Price, Margaret P Taugher, Rebecca J Grigsby, Daniel Ash, Jamison J Stark, Austin C Hossain Saad, Md Zubayer Singh, Kritika Mandal, Juthika Wemmie, John A Welsh, Michael J eLife Neuroscience Attenuating the strength of fearful memories could benefit people disabled by memories of past trauma. Pavlovian conditioning experiments indicate that a retrieval cue can return a conditioned aversive memory to a labile state. However, means to enhance retrieval and render a memory more labile are unknown. We hypothesized that augmenting synaptic signaling during retrieval would increase memory lability. To enhance synaptic transmission, mice inhaled CO(2) to induce an acidosis and activate acid sensing ion channels. Transient acidification increased the retrieval-induced lability of an aversive memory. The labile memory could then be weakened by an extinction protocol or strengthened by reconditioning. Coupling CO(2) inhalation to retrieval increased activation of amygdala neurons bearing the memory trace and increased the synaptic exchange from Ca(2+)-impermeable to Ca(2+)-permeable AMPA receptors. The results suggest that transient acidosis during retrieval renders the memory of an aversive event more labile and suggest a strategy to modify debilitating memories. DOI: http://dx.doi.org/10.7554/eLife.22564.001 eLife Sciences Publications, Ltd 2017-06-26 /pmc/articles/PMC5484615/ /pubmed/28650315 http://dx.doi.org/10.7554/eLife.22564 Text en © 2017, Du et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Du, Jianyang
Price, Margaret P
Taugher, Rebecca J
Grigsby, Daniel
Ash, Jamison J
Stark, Austin C
Hossain Saad, Md Zubayer
Singh, Kritika
Mandal, Juthika
Wemmie, John A
Welsh, Michael J
Transient acidosis while retrieving a fear-related memory enhances its lability
title Transient acidosis while retrieving a fear-related memory enhances its lability
title_full Transient acidosis while retrieving a fear-related memory enhances its lability
title_fullStr Transient acidosis while retrieving a fear-related memory enhances its lability
title_full_unstemmed Transient acidosis while retrieving a fear-related memory enhances its lability
title_short Transient acidosis while retrieving a fear-related memory enhances its lability
title_sort transient acidosis while retrieving a fear-related memory enhances its lability
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484615/
https://www.ncbi.nlm.nih.gov/pubmed/28650315
http://dx.doi.org/10.7554/eLife.22564
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