Cargando…

Central gene expression changes associated with enhanced neuroendocrine and autonomic response habituation to repeated noise stress after voluntary wheel running in rats

Accumulating evidence indicates that regular physical exercise benefits health in part by counteracting some of the negative physiological impacts of stress. While some studies identified reductions in some measures of acute stress responses with prior exercise, limited data were available concernin...

Descripción completa

Detalles Bibliográficos
Autores principales: Sasse, Sarah K., Nyhuis, Tara J., Masini, Cher V., Day, Heidi E. W., Campeau, Serge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3839297/
https://www.ncbi.nlm.nih.gov/pubmed/24324441
http://dx.doi.org/10.3389/fphys.2013.00341
_version_ 1782478420847886336
author Sasse, Sarah K.
Nyhuis, Tara J.
Masini, Cher V.
Day, Heidi E. W.
Campeau, Serge
author_facet Sasse, Sarah K.
Nyhuis, Tara J.
Masini, Cher V.
Day, Heidi E. W.
Campeau, Serge
author_sort Sasse, Sarah K.
collection PubMed
description Accumulating evidence indicates that regular physical exercise benefits health in part by counteracting some of the negative physiological impacts of stress. While some studies identified reductions in some measures of acute stress responses with prior exercise, limited data were available concerning effects on cardiovascular function, and reported effects on hypothalamic-pituitary-adrenocortical (HPA) axis responses were largely inconsistent. Given that exposure to repeated or prolonged stress is strongly implicated in the precipitation and exacerbation of illness, we proposed the novel hypothesis that physical exercise might facilitate adaptation to repeated stress, and subsequently demonstrated significant enhancement of both HPA axis (glucocorticoid) and cardiovascular (tachycardia) response habituation to repeated noise stress in rats with long-term access to running wheels compared to sedentary controls. Stress habituation has been attributed to modifications of brain circuits, but the specific sites of adaptation and the molecular changes driving its expression remain unclear. Here, in situ hybridization histochemistry was used to examine regulation of select stress-associated signaling systems in brain regions representing likely candidates to underlie exercise-enhanced stress habituation. Analyzed brains were collected from active (6 weeks of wheel running) and sedentary rats following control, acute, or repeated noise exposures that induced a significantly faster rate of glucocorticoid response habituation in active animals but preserved acute noise responsiveness. Nearly identical experimental manipulations also induce a faster rate of cardiovascular response habituation in exercised, repeatedly stressed rats. The observed regulation of the corticotropin-releasing factor and brain-derived neurotrophic factor systems across several brain regions suggests widespread effects of voluntary exercise on central functions and related adaptations to stress across multiple response modalities.
format Online
Article
Text
id pubmed-3839297
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-38392972013-12-09 Central gene expression changes associated with enhanced neuroendocrine and autonomic response habituation to repeated noise stress after voluntary wheel running in rats Sasse, Sarah K. Nyhuis, Tara J. Masini, Cher V. Day, Heidi E. W. Campeau, Serge Front Physiol Physiology Accumulating evidence indicates that regular physical exercise benefits health in part by counteracting some of the negative physiological impacts of stress. While some studies identified reductions in some measures of acute stress responses with prior exercise, limited data were available concerning effects on cardiovascular function, and reported effects on hypothalamic-pituitary-adrenocortical (HPA) axis responses were largely inconsistent. Given that exposure to repeated or prolonged stress is strongly implicated in the precipitation and exacerbation of illness, we proposed the novel hypothesis that physical exercise might facilitate adaptation to repeated stress, and subsequently demonstrated significant enhancement of both HPA axis (glucocorticoid) and cardiovascular (tachycardia) response habituation to repeated noise stress in rats with long-term access to running wheels compared to sedentary controls. Stress habituation has been attributed to modifications of brain circuits, but the specific sites of adaptation and the molecular changes driving its expression remain unclear. Here, in situ hybridization histochemistry was used to examine regulation of select stress-associated signaling systems in brain regions representing likely candidates to underlie exercise-enhanced stress habituation. Analyzed brains were collected from active (6 weeks of wheel running) and sedentary rats following control, acute, or repeated noise exposures that induced a significantly faster rate of glucocorticoid response habituation in active animals but preserved acute noise responsiveness. Nearly identical experimental manipulations also induce a faster rate of cardiovascular response habituation in exercised, repeatedly stressed rats. The observed regulation of the corticotropin-releasing factor and brain-derived neurotrophic factor systems across several brain regions suggests widespread effects of voluntary exercise on central functions and related adaptations to stress across multiple response modalities. Frontiers Media S.A. 2013-11-25 /pmc/articles/PMC3839297/ /pubmed/24324441 http://dx.doi.org/10.3389/fphys.2013.00341 Text en Copyright © 2013 Sasse, Nyhuis, Masini, Day and Campeau. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Sasse, Sarah K.
Nyhuis, Tara J.
Masini, Cher V.
Day, Heidi E. W.
Campeau, Serge
Central gene expression changes associated with enhanced neuroendocrine and autonomic response habituation to repeated noise stress after voluntary wheel running in rats
title Central gene expression changes associated with enhanced neuroendocrine and autonomic response habituation to repeated noise stress after voluntary wheel running in rats
title_full Central gene expression changes associated with enhanced neuroendocrine and autonomic response habituation to repeated noise stress after voluntary wheel running in rats
title_fullStr Central gene expression changes associated with enhanced neuroendocrine and autonomic response habituation to repeated noise stress after voluntary wheel running in rats
title_full_unstemmed Central gene expression changes associated with enhanced neuroendocrine and autonomic response habituation to repeated noise stress after voluntary wheel running in rats
title_short Central gene expression changes associated with enhanced neuroendocrine and autonomic response habituation to repeated noise stress after voluntary wheel running in rats
title_sort central gene expression changes associated with enhanced neuroendocrine and autonomic response habituation to repeated noise stress after voluntary wheel running in rats
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3839297/
https://www.ncbi.nlm.nih.gov/pubmed/24324441
http://dx.doi.org/10.3389/fphys.2013.00341
work_keys_str_mv AT sassesarahk centralgeneexpressionchangesassociatedwithenhancedneuroendocrineandautonomicresponsehabituationtorepeatednoisestressaftervoluntarywheelrunninginrats
AT nyhuistaraj centralgeneexpressionchangesassociatedwithenhancedneuroendocrineandautonomicresponsehabituationtorepeatednoisestressaftervoluntarywheelrunninginrats
AT masinicherv centralgeneexpressionchangesassociatedwithenhancedneuroendocrineandautonomicresponsehabituationtorepeatednoisestressaftervoluntarywheelrunninginrats
AT dayheidiew centralgeneexpressionchangesassociatedwithenhancedneuroendocrineandautonomicresponsehabituationtorepeatednoisestressaftervoluntarywheelrunninginrats
AT campeauserge centralgeneexpressionchangesassociatedwithenhancedneuroendocrineandautonomicresponsehabituationtorepeatednoisestressaftervoluntarywheelrunninginrats