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Anxiogenic Potential of Experimental Sleep Fragmentation Is Duration-Dependent and Mediated via Oxidative Stress State

Sleep architecture alterations, among which sleep fragmentation is highly prevalent, represent risk factors for a variety of diseases, ranging from cardiovascular to brain disorders, including anxiety. What mediates anxiety occurrence upon sleep fragmentation is still a matter of debate. We hypothes...

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Autores principales: Grubač, Željko, Šutulović, Nikola, Šuvakov, Sonja, Jerotić, Djurdja, Puškaš, Nela, Macut, Djuro, Rašić-Marković, Aleksandra, Simić, Tatjana, Stanojlović, Olivera, Hrnčić, Dragan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8405322/
https://www.ncbi.nlm.nih.gov/pubmed/34471462
http://dx.doi.org/10.1155/2021/2262913
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author Grubač, Željko
Šutulović, Nikola
Šuvakov, Sonja
Jerotić, Djurdja
Puškaš, Nela
Macut, Djuro
Rašić-Marković, Aleksandra
Simić, Tatjana
Stanojlović, Olivera
Hrnčić, Dragan
author_facet Grubač, Željko
Šutulović, Nikola
Šuvakov, Sonja
Jerotić, Djurdja
Puškaš, Nela
Macut, Djuro
Rašić-Marković, Aleksandra
Simić, Tatjana
Stanojlović, Olivera
Hrnčić, Dragan
author_sort Grubač, Željko
collection PubMed
description Sleep architecture alterations, among which sleep fragmentation is highly prevalent, represent risk factors for a variety of diseases, ranging from cardiovascular to brain disorders, including anxiety. What mediates anxiety occurrence upon sleep fragmentation is still a matter of debate. We hypothesized that the sleep fragmentation effects on anxiety are dependent on its duration and mediated by increased oxidative stress and alterations in the number of parvalbumin (PV+) interneurons in the hippocampus. Sleep was fragmented in rats by the treadmill method during a period of 14 days (SF group). Rats with undisturbed sleep in the treadmill (TC group) and those receiving equal amounts of treadmill belt motion (EC group) served as controls. To assess anxiety, we subjected rats to the open field, elevated plus maze, and light-dark tests on the 0, 7(th), and 14(th) day. Upon the last test, brain structures were sampled for oxidative stress assessment and PV+ interneuron immunohistochemistry. The results of ethological tests of anxiety-linked behavior suggested duration-dependent anxiogenic potential of sleep fragmentation. Rats' anxiety-linked behavior upon sleep fragmentation significantly correlated with oxidative stress. The rats with fragmented sleep (SF) showed significantly higher oxidative stress in the hippocampus, thalamus, and cortex, compared to controls (TC and EC), while the antioxidant enzymes' activity was significantly decreased. No significant differences were observed in hippocampal PV+ interneurons among these groups. Our results showed that duration of sleep fragmentation is a significant determinant of anxiety-linked behavior, and these effects are mediated through oxidative distress in the brain. Herein, it is revealed that the sleep fragmentation-oxidative stress-anxiety axis contributes to our better understanding of pathophysiological processes, occurring due to disrupted sleep patterns.
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spelling pubmed-84053222021-08-31 Anxiogenic Potential of Experimental Sleep Fragmentation Is Duration-Dependent and Mediated via Oxidative Stress State Grubač, Željko Šutulović, Nikola Šuvakov, Sonja Jerotić, Djurdja Puškaš, Nela Macut, Djuro Rašić-Marković, Aleksandra Simić, Tatjana Stanojlović, Olivera Hrnčić, Dragan Oxid Med Cell Longev Research Article Sleep architecture alterations, among which sleep fragmentation is highly prevalent, represent risk factors for a variety of diseases, ranging from cardiovascular to brain disorders, including anxiety. What mediates anxiety occurrence upon sleep fragmentation is still a matter of debate. We hypothesized that the sleep fragmentation effects on anxiety are dependent on its duration and mediated by increased oxidative stress and alterations in the number of parvalbumin (PV+) interneurons in the hippocampus. Sleep was fragmented in rats by the treadmill method during a period of 14 days (SF group). Rats with undisturbed sleep in the treadmill (TC group) and those receiving equal amounts of treadmill belt motion (EC group) served as controls. To assess anxiety, we subjected rats to the open field, elevated plus maze, and light-dark tests on the 0, 7(th), and 14(th) day. Upon the last test, brain structures were sampled for oxidative stress assessment and PV+ interneuron immunohistochemistry. The results of ethological tests of anxiety-linked behavior suggested duration-dependent anxiogenic potential of sleep fragmentation. Rats' anxiety-linked behavior upon sleep fragmentation significantly correlated with oxidative stress. The rats with fragmented sleep (SF) showed significantly higher oxidative stress in the hippocampus, thalamus, and cortex, compared to controls (TC and EC), while the antioxidant enzymes' activity was significantly decreased. No significant differences were observed in hippocampal PV+ interneurons among these groups. Our results showed that duration of sleep fragmentation is a significant determinant of anxiety-linked behavior, and these effects are mediated through oxidative distress in the brain. Herein, it is revealed that the sleep fragmentation-oxidative stress-anxiety axis contributes to our better understanding of pathophysiological processes, occurring due to disrupted sleep patterns. Hindawi 2021-08-21 /pmc/articles/PMC8405322/ /pubmed/34471462 http://dx.doi.org/10.1155/2021/2262913 Text en Copyright © 2021 Željko Grubač et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Grubač, Željko
Šutulović, Nikola
Šuvakov, Sonja
Jerotić, Djurdja
Puškaš, Nela
Macut, Djuro
Rašić-Marković, Aleksandra
Simić, Tatjana
Stanojlović, Olivera
Hrnčić, Dragan
Anxiogenic Potential of Experimental Sleep Fragmentation Is Duration-Dependent and Mediated via Oxidative Stress State
title Anxiogenic Potential of Experimental Sleep Fragmentation Is Duration-Dependent and Mediated via Oxidative Stress State
title_full Anxiogenic Potential of Experimental Sleep Fragmentation Is Duration-Dependent and Mediated via Oxidative Stress State
title_fullStr Anxiogenic Potential of Experimental Sleep Fragmentation Is Duration-Dependent and Mediated via Oxidative Stress State
title_full_unstemmed Anxiogenic Potential of Experimental Sleep Fragmentation Is Duration-Dependent and Mediated via Oxidative Stress State
title_short Anxiogenic Potential of Experimental Sleep Fragmentation Is Duration-Dependent and Mediated via Oxidative Stress State
title_sort anxiogenic potential of experimental sleep fragmentation is duration-dependent and mediated via oxidative stress state
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8405322/
https://www.ncbi.nlm.nih.gov/pubmed/34471462
http://dx.doi.org/10.1155/2021/2262913
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