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Functional organization of the midbrain periaqueductal gray for regulating aversive memory formation

Innately aversive experiences produce rapid defensive responses and powerful emotional memories. The midbrain periaqueductal gray (PAG) drives defensive behaviors through projections to brainstem motor control centers, but the PAG has also been implicated in aversive learning, receives information f...

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Autores principales: Yeh, Li-Feng, Ozawa, Takaaki, Johansen, Joshua P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424891/
https://www.ncbi.nlm.nih.gov/pubmed/34496926
http://dx.doi.org/10.1186/s13041-021-00844-0
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author Yeh, Li-Feng
Ozawa, Takaaki
Johansen, Joshua P.
author_facet Yeh, Li-Feng
Ozawa, Takaaki
Johansen, Joshua P.
author_sort Yeh, Li-Feng
collection PubMed
description Innately aversive experiences produce rapid defensive responses and powerful emotional memories. The midbrain periaqueductal gray (PAG) drives defensive behaviors through projections to brainstem motor control centers, but the PAG has also been implicated in aversive learning, receives information from aversive-signaling sensory systems and sends ascending projections to the thalamus as well as other forebrain structures which could control learning and memory. Here we sought to identify PAG subregions and cell types which instruct memory formation in response to aversive events. We found that optogenetic inhibition of neurons in the dorsolateral subregion of the PAG (dlPAG), but not the ventrolateral PAG (vlPAG), during an aversive event reduced memory formation. Furthermore, inhibition of a specific population of thalamus projecting dlPAG neurons projecting to the anterior paraventricular thalamus (aPVT) reduced aversive learning, but had no effect on the expression of previously learned defensive behaviors. By contrast, inactivation of dlPAG neurons which project to the posterior PVT (pPVT) or centromedial intralaminar thalamic nucleus (CM) had no effect on learning. These results reveal specific subregions and cell types within PAG responsible for its learning related functions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-021-00844-0.
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spelling pubmed-84248912021-09-10 Functional organization of the midbrain periaqueductal gray for regulating aversive memory formation Yeh, Li-Feng Ozawa, Takaaki Johansen, Joshua P. Mol Brain Research Innately aversive experiences produce rapid defensive responses and powerful emotional memories. The midbrain periaqueductal gray (PAG) drives defensive behaviors through projections to brainstem motor control centers, but the PAG has also been implicated in aversive learning, receives information from aversive-signaling sensory systems and sends ascending projections to the thalamus as well as other forebrain structures which could control learning and memory. Here we sought to identify PAG subregions and cell types which instruct memory formation in response to aversive events. We found that optogenetic inhibition of neurons in the dorsolateral subregion of the PAG (dlPAG), but not the ventrolateral PAG (vlPAG), during an aversive event reduced memory formation. Furthermore, inhibition of a specific population of thalamus projecting dlPAG neurons projecting to the anterior paraventricular thalamus (aPVT) reduced aversive learning, but had no effect on the expression of previously learned defensive behaviors. By contrast, inactivation of dlPAG neurons which project to the posterior PVT (pPVT) or centromedial intralaminar thalamic nucleus (CM) had no effect on learning. These results reveal specific subregions and cell types within PAG responsible for its learning related functions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-021-00844-0. BioMed Central 2021-09-08 /pmc/articles/PMC8424891/ /pubmed/34496926 http://dx.doi.org/10.1186/s13041-021-00844-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yeh, Li-Feng
Ozawa, Takaaki
Johansen, Joshua P.
Functional organization of the midbrain periaqueductal gray for regulating aversive memory formation
title Functional organization of the midbrain periaqueductal gray for regulating aversive memory formation
title_full Functional organization of the midbrain periaqueductal gray for regulating aversive memory formation
title_fullStr Functional organization of the midbrain periaqueductal gray for regulating aversive memory formation
title_full_unstemmed Functional organization of the midbrain periaqueductal gray for regulating aversive memory formation
title_short Functional organization of the midbrain periaqueductal gray for regulating aversive memory formation
title_sort functional organization of the midbrain periaqueductal gray for regulating aversive memory formation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424891/
https://www.ncbi.nlm.nih.gov/pubmed/34496926
http://dx.doi.org/10.1186/s13041-021-00844-0
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