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Bidirectional effects of voluntary exercise on the expression of Bdnf isoforms in the hippocampus of Hatano rat strains displaying different activity levels
Brain‐derived neurotrophic factor has functional mRNA isoforms, whose expression is assumed to mediate the beneficial effects of exercise in neuropsychiatric disorders. This study aims to reveal the mechanism of intensity‐dependent effects of voluntary exercise, focusing on the expression of Bdnf mR...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009423/ https://www.ncbi.nlm.nih.gov/pubmed/36649932 http://dx.doi.org/10.1002/npr2.12313 |
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author | Chiba, Shuichi Asano, Hikaru Moriya, Shogo Hatakeyama, Taichi Kobayashi, Shohei Ohta, Ryo Kawaguchi, Maiko |
author_facet | Chiba, Shuichi Asano, Hikaru Moriya, Shogo Hatakeyama, Taichi Kobayashi, Shohei Ohta, Ryo Kawaguchi, Maiko |
author_sort | Chiba, Shuichi |
collection | PubMed |
description | Brain‐derived neurotrophic factor has functional mRNA isoforms, whose expression is assumed to mediate the beneficial effects of exercise in neuropsychiatric disorders. This study aims to reveal the mechanism of intensity‐dependent effects of voluntary exercise, focusing on the expression of Bdnf mRNA isoforms in Hatano rats. Animals with different voluntary activity were housed in cages with a locked or unlocked wheel for 5 weeks. The expression levels of Bdnf isoforms and the corresponding coding sequences (CDS) were measured in the hippocampus using real‐time polymerase chain reaction (PCR). We found that exercise increased the expression of Bdnf isoform containing exon 1 in the high‐intensity‐running strain and decreased the expressions of Bdnf exon 1, 3, 6, 7, 8, and 9a in mild‐intensity‐running animal. The expression of Bdnf CDS was increased by exercise in both strains. These results suggest that expressions of Bdnf isoforms depend on the intensities of voluntary exercise, but the involvement of subjects' genetic background could not be excluded. Our finding also implies that the bidirectional effects of exercise may not be mediated via the final product of Bdnf. |
format | Online Article Text |
id | pubmed-10009423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100094232023-03-14 Bidirectional effects of voluntary exercise on the expression of Bdnf isoforms in the hippocampus of Hatano rat strains displaying different activity levels Chiba, Shuichi Asano, Hikaru Moriya, Shogo Hatakeyama, Taichi Kobayashi, Shohei Ohta, Ryo Kawaguchi, Maiko Neuropsychopharmacol Rep Micro Reports Brain‐derived neurotrophic factor has functional mRNA isoforms, whose expression is assumed to mediate the beneficial effects of exercise in neuropsychiatric disorders. This study aims to reveal the mechanism of intensity‐dependent effects of voluntary exercise, focusing on the expression of Bdnf mRNA isoforms in Hatano rats. Animals with different voluntary activity were housed in cages with a locked or unlocked wheel for 5 weeks. The expression levels of Bdnf isoforms and the corresponding coding sequences (CDS) were measured in the hippocampus using real‐time polymerase chain reaction (PCR). We found that exercise increased the expression of Bdnf isoform containing exon 1 in the high‐intensity‐running strain and decreased the expressions of Bdnf exon 1, 3, 6, 7, 8, and 9a in mild‐intensity‐running animal. The expression of Bdnf CDS was increased by exercise in both strains. These results suggest that expressions of Bdnf isoforms depend on the intensities of voluntary exercise, but the involvement of subjects' genetic background could not be excluded. Our finding also implies that the bidirectional effects of exercise may not be mediated via the final product of Bdnf. John Wiley and Sons Inc. 2023-01-17 /pmc/articles/PMC10009423/ /pubmed/36649932 http://dx.doi.org/10.1002/npr2.12313 Text en © 2023 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Neuropsychopharmacology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Micro Reports Chiba, Shuichi Asano, Hikaru Moriya, Shogo Hatakeyama, Taichi Kobayashi, Shohei Ohta, Ryo Kawaguchi, Maiko Bidirectional effects of voluntary exercise on the expression of Bdnf isoforms in the hippocampus of Hatano rat strains displaying different activity levels |
title | Bidirectional effects of voluntary exercise on the expression of Bdnf isoforms in the hippocampus of Hatano rat strains displaying different activity levels |
title_full | Bidirectional effects of voluntary exercise on the expression of Bdnf isoforms in the hippocampus of Hatano rat strains displaying different activity levels |
title_fullStr | Bidirectional effects of voluntary exercise on the expression of Bdnf isoforms in the hippocampus of Hatano rat strains displaying different activity levels |
title_full_unstemmed | Bidirectional effects of voluntary exercise on the expression of Bdnf isoforms in the hippocampus of Hatano rat strains displaying different activity levels |
title_short | Bidirectional effects of voluntary exercise on the expression of Bdnf isoforms in the hippocampus of Hatano rat strains displaying different activity levels |
title_sort | bidirectional effects of voluntary exercise on the expression of bdnf isoforms in the hippocampus of hatano rat strains displaying different activity levels |
topic | Micro Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009423/ https://www.ncbi.nlm.nih.gov/pubmed/36649932 http://dx.doi.org/10.1002/npr2.12313 |
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