Cargando…

Effects of exercise on brain and peripheral inflammatory biomarkers induced by total sleep deprivation in rats

BACKGROUND: Physical exercise induces neuroprotection through anti-inflammatory effects and total sleep deprivation is reported an inflammatory process. We examined whether 7 weeks of exercise training attenuates markers of inflammation during total sleep deprivation (24-h wakefulness) in the rat br...

Descripción completa

Detalles Bibliográficos
Autores principales: Chennaoui, M., Gomez-Merino, D., Drogou, C., Geoffroy, H., Dispersyn, G., Langrume, C., Ciret, S., Gallopin, T., Sauvet, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588685/
https://www.ncbi.nlm.nih.gov/pubmed/26425116
http://dx.doi.org/10.1186/s12950-015-0102-3
_version_ 1782392672036585472
author Chennaoui, M.
Gomez-Merino, D.
Drogou, C.
Geoffroy, H.
Dispersyn, G.
Langrume, C.
Ciret, S.
Gallopin, T.
Sauvet, F.
author_facet Chennaoui, M.
Gomez-Merino, D.
Drogou, C.
Geoffroy, H.
Dispersyn, G.
Langrume, C.
Ciret, S.
Gallopin, T.
Sauvet, F.
author_sort Chennaoui, M.
collection PubMed
description BACKGROUND: Physical exercise induces neuroprotection through anti-inflammatory effects and total sleep deprivation is reported an inflammatory process. We examined whether 7 weeks of exercise training attenuates markers of inflammation during total sleep deprivation (24-h wakefulness) in the rat brain and periphery. METHODS: Four groups of 10 rats were investigated: Sedentary control, Sedentary sleep-deprived, Exercised control, and Exercised sleep-deprived. Sleep deprivation and exercise training were induced using slowly rotating wheels and a motorized treadmill. We examined mRNA expression of pro-inflammatory (IL-1β, TNF-α, and IL-6) cytokine-related genes using real-time PCR, and protein levels in the hippocampus and frontal cortex, as well as circulating concentrations. RESULTS: Compared to Sedentary control rats, hippocampal and cortical IL-1β mRNA expressions in Sedentary sleep-deprived rats were up-regulated (p < 0.05 and p < 0.01 respectively). At the protein level, hippocampal IL-1β and TNF-α and cortical IL-6 contents were higher in Sedentary sleep-deprived rats (p < 0.001, p < 0.05, p < 0.05, respectively). Peripherally, TNF-α, IL-6 and norepinephrine concentrations were higher in Sedentary sleep-deprived rats compared to Sedentary control (p < 0.01, p < 0.001, p < 0.01, respectively). Exercise training reduced the sleep deprivation-induced hippocampal IL-1β increases (mRNA expression and protein content) (p < 0.05 and p < 0.001), and TNF-α content (p < 0.001). At the periphery, exercise reduced sleep deprivation-induced increase of IL-6 concentration (p < 0.05) without effect on TNF-α and norepinephrine. CONCLUSIONS: We demonstrate that a 7-week exercise training program before acute total sleep deprivation prevents pro-inflammatory responses in the rat hippocampus, particularly the IL-1β cytokine at the gene expression level and protein content.
format Online
Article
Text
id pubmed-4588685
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-45886852015-10-01 Effects of exercise on brain and peripheral inflammatory biomarkers induced by total sleep deprivation in rats Chennaoui, M. Gomez-Merino, D. Drogou, C. Geoffroy, H. Dispersyn, G. Langrume, C. Ciret, S. Gallopin, T. Sauvet, F. J Inflamm (Lond) Research BACKGROUND: Physical exercise induces neuroprotection through anti-inflammatory effects and total sleep deprivation is reported an inflammatory process. We examined whether 7 weeks of exercise training attenuates markers of inflammation during total sleep deprivation (24-h wakefulness) in the rat brain and periphery. METHODS: Four groups of 10 rats were investigated: Sedentary control, Sedentary sleep-deprived, Exercised control, and Exercised sleep-deprived. Sleep deprivation and exercise training were induced using slowly rotating wheels and a motorized treadmill. We examined mRNA expression of pro-inflammatory (IL-1β, TNF-α, and IL-6) cytokine-related genes using real-time PCR, and protein levels in the hippocampus and frontal cortex, as well as circulating concentrations. RESULTS: Compared to Sedentary control rats, hippocampal and cortical IL-1β mRNA expressions in Sedentary sleep-deprived rats were up-regulated (p < 0.05 and p < 0.01 respectively). At the protein level, hippocampal IL-1β and TNF-α and cortical IL-6 contents were higher in Sedentary sleep-deprived rats (p < 0.001, p < 0.05, p < 0.05, respectively). Peripherally, TNF-α, IL-6 and norepinephrine concentrations were higher in Sedentary sleep-deprived rats compared to Sedentary control (p < 0.01, p < 0.001, p < 0.01, respectively). Exercise training reduced the sleep deprivation-induced hippocampal IL-1β increases (mRNA expression and protein content) (p < 0.05 and p < 0.001), and TNF-α content (p < 0.001). At the periphery, exercise reduced sleep deprivation-induced increase of IL-6 concentration (p < 0.05) without effect on TNF-α and norepinephrine. CONCLUSIONS: We demonstrate that a 7-week exercise training program before acute total sleep deprivation prevents pro-inflammatory responses in the rat hippocampus, particularly the IL-1β cytokine at the gene expression level and protein content. BioMed Central 2015-09-30 /pmc/articles/PMC4588685/ /pubmed/26425116 http://dx.doi.org/10.1186/s12950-015-0102-3 Text en © Chennaoui et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Chennaoui, M.
Gomez-Merino, D.
Drogou, C.
Geoffroy, H.
Dispersyn, G.
Langrume, C.
Ciret, S.
Gallopin, T.
Sauvet, F.
Effects of exercise on brain and peripheral inflammatory biomarkers induced by total sleep deprivation in rats
title Effects of exercise on brain and peripheral inflammatory biomarkers induced by total sleep deprivation in rats
title_full Effects of exercise on brain and peripheral inflammatory biomarkers induced by total sleep deprivation in rats
title_fullStr Effects of exercise on brain and peripheral inflammatory biomarkers induced by total sleep deprivation in rats
title_full_unstemmed Effects of exercise on brain and peripheral inflammatory biomarkers induced by total sleep deprivation in rats
title_short Effects of exercise on brain and peripheral inflammatory biomarkers induced by total sleep deprivation in rats
title_sort effects of exercise on brain and peripheral inflammatory biomarkers induced by total sleep deprivation in rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588685/
https://www.ncbi.nlm.nih.gov/pubmed/26425116
http://dx.doi.org/10.1186/s12950-015-0102-3
work_keys_str_mv AT chennaouim effectsofexerciseonbrainandperipheralinflammatorybiomarkersinducedbytotalsleepdeprivationinrats
AT gomezmerinod effectsofexerciseonbrainandperipheralinflammatorybiomarkersinducedbytotalsleepdeprivationinrats
AT drogouc effectsofexerciseonbrainandperipheralinflammatorybiomarkersinducedbytotalsleepdeprivationinrats
AT geoffroyh effectsofexerciseonbrainandperipheralinflammatorybiomarkersinducedbytotalsleepdeprivationinrats
AT dispersyng effectsofexerciseonbrainandperipheralinflammatorybiomarkersinducedbytotalsleepdeprivationinrats
AT langrumec effectsofexerciseonbrainandperipheralinflammatorybiomarkersinducedbytotalsleepdeprivationinrats
AT cirets effectsofexerciseonbrainandperipheralinflammatorybiomarkersinducedbytotalsleepdeprivationinrats
AT gallopint effectsofexerciseonbrainandperipheralinflammatorybiomarkersinducedbytotalsleepdeprivationinrats
AT sauvetf effectsofexerciseonbrainandperipheralinflammatorybiomarkersinducedbytotalsleepdeprivationinrats