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Metabolic fingerprints of fear memory consolidation during sleep

Metabolites underlying brain function and pathology are not as well understood as genes. Here, we applied a novel metabolomics approach to further understand the mechanisms of memory processing in sleep. As hippocampal dentate gyrus neurons are known to consolidate contextual fear memory, we analyze...

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Autores principales: Koyanagi, Iyo, Sonomura, Kazuhiro, Naoi, Toshie, Ohnishi, Takaaki, Kaneko, Naoko, Sawamoto, Kazunobu, Sato, Taka-Aki, Sakaguchi, Masanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874630/
https://www.ncbi.nlm.nih.gov/pubmed/33568175
http://dx.doi.org/10.1186/s13041-021-00733-6
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author Koyanagi, Iyo
Sonomura, Kazuhiro
Naoi, Toshie
Ohnishi, Takaaki
Kaneko, Naoko
Sawamoto, Kazunobu
Sato, Taka-Aki
Sakaguchi, Masanori
author_facet Koyanagi, Iyo
Sonomura, Kazuhiro
Naoi, Toshie
Ohnishi, Takaaki
Kaneko, Naoko
Sawamoto, Kazunobu
Sato, Taka-Aki
Sakaguchi, Masanori
author_sort Koyanagi, Iyo
collection PubMed
description Metabolites underlying brain function and pathology are not as well understood as genes. Here, we applied a novel metabolomics approach to further understand the mechanisms of memory processing in sleep. As hippocampal dentate gyrus neurons are known to consolidate contextual fear memory, we analyzed real-time changes in metabolites in the dentate gyrus in different sleep–wake states in mice. Throughout the study, we consistently detected more than > 200 metabolites. Metabolite profiles changed dramactically upon sleep–wake state transitions, leading to a clear separation of phenotypes between wakefulness and sleep. By contrast, contextual fear memory consolidation induced less obvious metabolite phenotypes. However, changes in purine metabolites were observed upon both sleep–wake state transitions and contextual fear memory consolidation. Dietary supplementation of certain purine metabolites impaired correlations between conditioned fear responses before and after memory consolidation. These results point toward the importance of purine metabolism in fear memory processing during sleep.
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spelling pubmed-78746302021-02-11 Metabolic fingerprints of fear memory consolidation during sleep Koyanagi, Iyo Sonomura, Kazuhiro Naoi, Toshie Ohnishi, Takaaki Kaneko, Naoko Sawamoto, Kazunobu Sato, Taka-Aki Sakaguchi, Masanori Mol Brain Research Metabolites underlying brain function and pathology are not as well understood as genes. Here, we applied a novel metabolomics approach to further understand the mechanisms of memory processing in sleep. As hippocampal dentate gyrus neurons are known to consolidate contextual fear memory, we analyzed real-time changes in metabolites in the dentate gyrus in different sleep–wake states in mice. Throughout the study, we consistently detected more than > 200 metabolites. Metabolite profiles changed dramactically upon sleep–wake state transitions, leading to a clear separation of phenotypes between wakefulness and sleep. By contrast, contextual fear memory consolidation induced less obvious metabolite phenotypes. However, changes in purine metabolites were observed upon both sleep–wake state transitions and contextual fear memory consolidation. Dietary supplementation of certain purine metabolites impaired correlations between conditioned fear responses before and after memory consolidation. These results point toward the importance of purine metabolism in fear memory processing during sleep. BioMed Central 2021-02-10 /pmc/articles/PMC7874630/ /pubmed/33568175 http://dx.doi.org/10.1186/s13041-021-00733-6 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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
Koyanagi, Iyo
Sonomura, Kazuhiro
Naoi, Toshie
Ohnishi, Takaaki
Kaneko, Naoko
Sawamoto, Kazunobu
Sato, Taka-Aki
Sakaguchi, Masanori
Metabolic fingerprints of fear memory consolidation during sleep
title Metabolic fingerprints of fear memory consolidation during sleep
title_full Metabolic fingerprints of fear memory consolidation during sleep
title_fullStr Metabolic fingerprints of fear memory consolidation during sleep
title_full_unstemmed Metabolic fingerprints of fear memory consolidation during sleep
title_short Metabolic fingerprints of fear memory consolidation during sleep
title_sort metabolic fingerprints of fear memory consolidation during sleep
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874630/
https://www.ncbi.nlm.nih.gov/pubmed/33568175
http://dx.doi.org/10.1186/s13041-021-00733-6
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