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Effects of Supraphysiological Doses of Sex Steroids on Wheel Running Activity in Mice
The regulatory mechanisms of physical activity are postulated to include environmental and biological/genetic factors. In particular, the sex steroids appear to have profound effects on wheel running in rodents. The purpose of this project was to investigate the effects of 17β-estradiol and testoste...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236312/ https://www.ncbi.nlm.nih.gov/pubmed/25419484 http://dx.doi.org/10.4172/2157-7536.1000110 |
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author | Bowen, Robert S Knab, Amy M Hamilton, Alicia Trynor McCall, Jennifer R Moore-Harrison, Trudy L Lightfoot, J Timothy |
author_facet | Bowen, Robert S Knab, Amy M Hamilton, Alicia Trynor McCall, Jennifer R Moore-Harrison, Trudy L Lightfoot, J Timothy |
author_sort | Bowen, Robert S |
collection | PubMed |
description | The regulatory mechanisms of physical activity are postulated to include environmental and biological/genetic factors. In particular, the sex steroids appear to have profound effects on wheel running in rodents. The purpose of this project was to investigate the effects of 17β-estradiol and testosterone on wheel running distance, duration, and speed in male and female C57BL/6J mice. The mice (N=46) were provided free access to running wheels interfaced with computers to track daily running distance, duration, and speed. Activity was assessed at baseline in intact mice, after surgical gonadectomy, and after replacement with either 17β-estradiol or testosterone. Upon removal of the gonads, physical activity levels were significantly reduced in both males and females. Distance (10–30% of baseline) and duration (20–47% of baseline) measures were most affected by the loss of endogenous steroids, while running speed (60–77% of baseline) though significantly reduced-decreased by a much lower magnitude. Testosterone replacement fully recovered running distance, duration, and speed to pre-surgical levels in both sexes (100% of baseline). Distance (30–42% of baseline) and duration (43–47% of baseline) were partially recovered by 17β-estradiol, but not to baseline levels. Speed (100% of baseline) was fully recovered by 17β-estradiol replacement in males and females. This study suggests that physical activity in mice is affected by endogenous steroids and can be altered by exogenous steroid replacement. The differences in the recovery abilities of 17β-estradiol and testosterone suggest that both estrogenic and androgenic pathways may be involved to variable degrees in activity regulation. |
format | Online Article Text |
id | pubmed-4236312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-42363122014-11-19 Effects of Supraphysiological Doses of Sex Steroids on Wheel Running Activity in Mice Bowen, Robert S Knab, Amy M Hamilton, Alicia Trynor McCall, Jennifer R Moore-Harrison, Trudy L Lightfoot, J Timothy J Steroids Horm Sci Article The regulatory mechanisms of physical activity are postulated to include environmental and biological/genetic factors. In particular, the sex steroids appear to have profound effects on wheel running in rodents. The purpose of this project was to investigate the effects of 17β-estradiol and testosterone on wheel running distance, duration, and speed in male and female C57BL/6J mice. The mice (N=46) were provided free access to running wheels interfaced with computers to track daily running distance, duration, and speed. Activity was assessed at baseline in intact mice, after surgical gonadectomy, and after replacement with either 17β-estradiol or testosterone. Upon removal of the gonads, physical activity levels were significantly reduced in both males and females. Distance (10–30% of baseline) and duration (20–47% of baseline) measures were most affected by the loss of endogenous steroids, while running speed (60–77% of baseline) though significantly reduced-decreased by a much lower magnitude. Testosterone replacement fully recovered running distance, duration, and speed to pre-surgical levels in both sexes (100% of baseline). Distance (30–42% of baseline) and duration (43–47% of baseline) were partially recovered by 17β-estradiol, but not to baseline levels. Speed (100% of baseline) was fully recovered by 17β-estradiol replacement in males and females. This study suggests that physical activity in mice is affected by endogenous steroids and can be altered by exogenous steroid replacement. The differences in the recovery abilities of 17β-estradiol and testosterone suggest that both estrogenic and androgenic pathways may be involved to variable degrees in activity regulation. 2012-07-09 2012-11-01 /pmc/articles/PMC4236312/ /pubmed/25419484 http://dx.doi.org/10.4172/2157-7536.1000110 Text en © 2012 Bowen RS, et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Bowen, Robert S Knab, Amy M Hamilton, Alicia Trynor McCall, Jennifer R Moore-Harrison, Trudy L Lightfoot, J Timothy Effects of Supraphysiological Doses of Sex Steroids on Wheel Running Activity in Mice |
title | Effects of Supraphysiological Doses of Sex Steroids on Wheel Running Activity in Mice |
title_full | Effects of Supraphysiological Doses of Sex Steroids on Wheel Running Activity in Mice |
title_fullStr | Effects of Supraphysiological Doses of Sex Steroids on Wheel Running Activity in Mice |
title_full_unstemmed | Effects of Supraphysiological Doses of Sex Steroids on Wheel Running Activity in Mice |
title_short | Effects of Supraphysiological Doses of Sex Steroids on Wheel Running Activity in Mice |
title_sort | effects of supraphysiological doses of sex steroids on wheel running activity in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236312/ https://www.ncbi.nlm.nih.gov/pubmed/25419484 http://dx.doi.org/10.4172/2157-7536.1000110 |
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