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Cage restriction‐induced physical inactivity promotes subsequent hepatic apoptosis during tail suspension in young male rats
This study investigated the impact of long‐term physical inactivity on hepatic cytoprotective‐ and inflammatory‐related protein expressions in young rats and the subsequent apoptotic response during microgravity stress simulated by tail suspension. Four‐week‐old male Wistar rats were randomly assign...
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/PMC10209429/ https://www.ncbi.nlm.nih.gov/pubmed/37226378 http://dx.doi.org/10.14814/phy2.15695 |
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author | Dobashi, Shohei Naito, Hisashi Yoshihara, Toshinori |
author_facet | Dobashi, Shohei Naito, Hisashi Yoshihara, Toshinori |
author_sort | Dobashi, Shohei |
collection | PubMed |
description | This study investigated the impact of long‐term physical inactivity on hepatic cytoprotective‐ and inflammatory‐related protein expressions in young rats and the subsequent apoptotic response during microgravity stress simulated by tail suspension. Four‐week‐old male Wistar rats were randomly assigned to the control (CT) and physical inactivity (IN) groups. The floor space of the cages provided to the IN group was reduced to half of that provided to the CT group. After 8 weeks, rats in both groups (n = 6–7) underwent tail suspension. Their livers were harvested immediately before (0 day) or 1, 3, and 7 days after tail suspension. Levels of hepatic heat shock protein 72 (HSP72), an anti‐apoptotic protein, reduced over 7 days of tail suspension in the IN group than in the CT group (p < 0.01). Fragmented nucleosomes in the cytoplasmic fraction of the liver, an apoptotic index, were drastically increased by physical inactivity and tail suspension, and this change was significantly greater after 7 days of tail suspension in the IN group than in the CT group (p < 0.01). The apoptotic response was accompanied by the upregulation of pro‐apoptotic proteins (cleaved caspase‐3 and ‐7). Moreover, the levels of other pro‐apoptotic proteins (tumor necrosis factor‐1α and histone deacetylase 5) were also significantly higher in the IN than in the CT group (p < 0.05). Our results indicated that 8 weeks of physical inactivity decreased hepatic HSP72 levels and promoted hepatic apoptosis during the subsequent 7 days of tail suspension. |
format | Online Article Text |
id | pubmed-10209429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102094292023-05-26 Cage restriction‐induced physical inactivity promotes subsequent hepatic apoptosis during tail suspension in young male rats Dobashi, Shohei Naito, Hisashi Yoshihara, Toshinori Physiol Rep Original Articles This study investigated the impact of long‐term physical inactivity on hepatic cytoprotective‐ and inflammatory‐related protein expressions in young rats and the subsequent apoptotic response during microgravity stress simulated by tail suspension. Four‐week‐old male Wistar rats were randomly assigned to the control (CT) and physical inactivity (IN) groups. The floor space of the cages provided to the IN group was reduced to half of that provided to the CT group. After 8 weeks, rats in both groups (n = 6–7) underwent tail suspension. Their livers were harvested immediately before (0 day) or 1, 3, and 7 days after tail suspension. Levels of hepatic heat shock protein 72 (HSP72), an anti‐apoptotic protein, reduced over 7 days of tail suspension in the IN group than in the CT group (p < 0.01). Fragmented nucleosomes in the cytoplasmic fraction of the liver, an apoptotic index, were drastically increased by physical inactivity and tail suspension, and this change was significantly greater after 7 days of tail suspension in the IN group than in the CT group (p < 0.01). The apoptotic response was accompanied by the upregulation of pro‐apoptotic proteins (cleaved caspase‐3 and ‐7). Moreover, the levels of other pro‐apoptotic proteins (tumor necrosis factor‐1α and histone deacetylase 5) were also significantly higher in the IN than in the CT group (p < 0.05). Our results indicated that 8 weeks of physical inactivity decreased hepatic HSP72 levels and promoted hepatic apoptosis during the subsequent 7 days of tail suspension. John Wiley and Sons Inc. 2023-05-24 /pmc/articles/PMC10209429/ /pubmed/37226378 http://dx.doi.org/10.14814/phy2.15695 Text en © 2023 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Dobashi, Shohei Naito, Hisashi Yoshihara, Toshinori Cage restriction‐induced physical inactivity promotes subsequent hepatic apoptosis during tail suspension in young male rats |
title | Cage restriction‐induced physical inactivity promotes subsequent hepatic apoptosis during tail suspension in young male rats |
title_full | Cage restriction‐induced physical inactivity promotes subsequent hepatic apoptosis during tail suspension in young male rats |
title_fullStr | Cage restriction‐induced physical inactivity promotes subsequent hepatic apoptosis during tail suspension in young male rats |
title_full_unstemmed | Cage restriction‐induced physical inactivity promotes subsequent hepatic apoptosis during tail suspension in young male rats |
title_short | Cage restriction‐induced physical inactivity promotes subsequent hepatic apoptosis during tail suspension in young male rats |
title_sort | cage restriction‐induced physical inactivity promotes subsequent hepatic apoptosis during tail suspension in young male rats |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209429/ https://www.ncbi.nlm.nih.gov/pubmed/37226378 http://dx.doi.org/10.14814/phy2.15695 |
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