Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1783649623662919680 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7874630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT koyanagiiyo metabolicfingerprintsoffearmemoryconsolidationduringsleep AT sonomurakazuhiro metabolicfingerprintsoffearmemoryconsolidationduringsleep AT naoitoshie metabolicfingerprintsoffearmemoryconsolidationduringsleep AT ohnishitakaaki metabolicfingerprintsoffearmemoryconsolidationduringsleep AT kanekonaoko metabolicfingerprintsoffearmemoryconsolidationduringsleep AT sawamotokazunobu metabolicfingerprintsoffearmemoryconsolidationduringsleep AT satotakaaki metabolicfingerprintsoffearmemoryconsolidationduringsleep AT sakaguchimasanori metabolicfingerprintsoffearmemoryconsolidationduringsleep |