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Prefrontal engrams of long-term fear memory perpetuate pain perception
A painful episode can lead to a life-long increase in an individual’s experience of pain. Fearful anticipation of imminent pain could play a role in this phenomenon, but the neurobiological underpinnings are unclear because fear can both suppress and enhance pain. Here, we show in mice that long-ter...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166861/ https://www.ncbi.nlm.nih.gov/pubmed/37024573 http://dx.doi.org/10.1038/s41593-023-01291-x |
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author | Stegemann, Alina Liu, Sheng Retana Romero, Oscar Andrés Oswald, Manfred Josef Han, Yechao Beretta, Carlo Antonio Gan, Zheng Tan, Linette Liqi Wisden, William Gräff, Johannes Kuner, Rohini |
author_facet | Stegemann, Alina Liu, Sheng Retana Romero, Oscar Andrés Oswald, Manfred Josef Han, Yechao Beretta, Carlo Antonio Gan, Zheng Tan, Linette Liqi Wisden, William Gräff, Johannes Kuner, Rohini |
author_sort | Stegemann, Alina |
collection | PubMed |
description | A painful episode can lead to a life-long increase in an individual’s experience of pain. Fearful anticipation of imminent pain could play a role in this phenomenon, but the neurobiological underpinnings are unclear because fear can both suppress and enhance pain. Here, we show in mice that long-term associative fear memory stored in neuronal engrams in the prefrontal cortex determines whether a painful episode shapes pain experience later in life. Furthermore, under conditions of inflammatory and neuropathic pain, prefrontal fear engrams expand to encompass neurons representing nociception and tactile sensation, leading to pronounced changes in prefrontal connectivity to fear-relevant brain areas. Conversely, silencing prefrontal fear engrams reverses chronically established hyperalgesia and allodynia. These results reveal that a discrete subset of prefrontal cortex neurons can account for the debilitating comorbidity of fear and chronic pain and show that attenuating the fear memory of pain can alleviate chronic pain itself. |
format | Online Article Text |
id | pubmed-10166861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-101668612023-05-10 Prefrontal engrams of long-term fear memory perpetuate pain perception Stegemann, Alina Liu, Sheng Retana Romero, Oscar Andrés Oswald, Manfred Josef Han, Yechao Beretta, Carlo Antonio Gan, Zheng Tan, Linette Liqi Wisden, William Gräff, Johannes Kuner, Rohini Nat Neurosci Article A painful episode can lead to a life-long increase in an individual’s experience of pain. Fearful anticipation of imminent pain could play a role in this phenomenon, but the neurobiological underpinnings are unclear because fear can both suppress and enhance pain. Here, we show in mice that long-term associative fear memory stored in neuronal engrams in the prefrontal cortex determines whether a painful episode shapes pain experience later in life. Furthermore, under conditions of inflammatory and neuropathic pain, prefrontal fear engrams expand to encompass neurons representing nociception and tactile sensation, leading to pronounced changes in prefrontal connectivity to fear-relevant brain areas. Conversely, silencing prefrontal fear engrams reverses chronically established hyperalgesia and allodynia. These results reveal that a discrete subset of prefrontal cortex neurons can account for the debilitating comorbidity of fear and chronic pain and show that attenuating the fear memory of pain can alleviate chronic pain itself. Nature Publishing Group US 2023-04-06 2023 /pmc/articles/PMC10166861/ /pubmed/37024573 http://dx.doi.org/10.1038/s41593-023-01291-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Stegemann, Alina Liu, Sheng Retana Romero, Oscar Andrés Oswald, Manfred Josef Han, Yechao Beretta, Carlo Antonio Gan, Zheng Tan, Linette Liqi Wisden, William Gräff, Johannes Kuner, Rohini Prefrontal engrams of long-term fear memory perpetuate pain perception |
title | Prefrontal engrams of long-term fear memory perpetuate pain perception |
title_full | Prefrontal engrams of long-term fear memory perpetuate pain perception |
title_fullStr | Prefrontal engrams of long-term fear memory perpetuate pain perception |
title_full_unstemmed | Prefrontal engrams of long-term fear memory perpetuate pain perception |
title_short | Prefrontal engrams of long-term fear memory perpetuate pain perception |
title_sort | prefrontal engrams of long-term fear memory perpetuate pain perception |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166861/ https://www.ncbi.nlm.nih.gov/pubmed/37024573 http://dx.doi.org/10.1038/s41593-023-01291-x |
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