The Impact of Chronic Sleep Restriction on Neuronal Number and Volumetric Correlates of the Dorsal Respiratory Nuclei in a Rat Model

Abstract Study Objectives Sleep restriction can result in a range of neurophysiological consequences in the brain including some brain stem nuclei. This study aimed to evaluate the effects of chronic sleep restriction (CSR) on quantitative aspects of brain stem respiratory centers using stereologica...

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Veröffentlicht in:Sleep (New York, N.Y.) N.Y.), 2017-08, Vol.40 (8)
Hauptverfasser: Kamali, Ali-Mohammad, Noorafshan, Ali, Karimi, Fatemeh, Karbalay-Doust, Saied, Nami, Mohammad
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container_issue 8
container_start_page
container_title Sleep (New York, N.Y.)
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creator Kamali, Ali-Mohammad
Noorafshan, Ali
Karimi, Fatemeh
Karbalay-Doust, Saied
Nami, Mohammad
description Abstract Study Objectives Sleep restriction can result in a range of neurophysiological consequences in the brain including some brain stem nuclei. This study aimed to evaluate the effects of chronic sleep restriction (CSR) on quantitative aspects of brain stem respiratory centers using stereological methods. Methods Male rats were randomly assigned into experimental group (CSR through a modified multiple platform apparatus), corresponding apparatus-control group (grid-floor control) and cage controls. In the grid-floor control group, animals were placed on wire-mesh grids positioned upon CSR apparatus and were then allowed to retain the opportunity to sleep. On day 21, all rats were euthanized with their brains removed for stereological assessments. The nuclei which are known to be involved in respiration rhythm including nucleus tractus solitarius (NTS), parabrachial nuclei (PB), and Kölliker–Fuse nucleus (KF) were evaluated. Results Compared to the control groups, stereological findings in CSR rats revealed a decrease by 5.2 ± 0.01%, 7.1 ± 0.007%, 3.9 ± 0.004%, and 6.3 ± 0.002% (mean ± standard error of the mean [SEM], p < .01 for all) in the volume of NTS, medial PB, lateral PB, and KF nuclei, respectively. Also, the total neuronal number of NTS, medial PB, lateral PB, and KF showed a significant decrease by 10.2 ± 21.4%, 6.3 ± 5.2%, 11.8 ± 8.6%, and 9.3 ± 2.5% (mean ± SEM, p < .05 for all), respectively. Conclusions CSR may potentially induce neuronal loss and structural changes in the dorsal respiratory nuclei.
doi_str_mv 10.1093/sleep/zsx072
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This study aimed to evaluate the effects of chronic sleep restriction (CSR) on quantitative aspects of brain stem respiratory centers using stereological methods. Methods Male rats were randomly assigned into experimental group (CSR through a modified multiple platform apparatus), corresponding apparatus-control group (grid-floor control) and cage controls. In the grid-floor control group, animals were placed on wire-mesh grids positioned upon CSR apparatus and were then allowed to retain the opportunity to sleep. On day 21, all rats were euthanized with their brains removed for stereological assessments. The nuclei which are known to be involved in respiration rhythm including nucleus tractus solitarius (NTS), parabrachial nuclei (PB), and Kölliker–Fuse nucleus (KF) were evaluated. Results Compared to the control groups, stereological findings in CSR rats revealed a decrease by 5.2 ± 0.01%, 7.1 ± 0.007%, 3.9 ± 0.004%, and 6.3 ± 0.002% (mean ± standard error of the mean [SEM], p &lt; .01 for all) in the volume of NTS, medial PB, lateral PB, and KF nuclei, respectively. Also, the total neuronal number of NTS, medial PB, lateral PB, and KF showed a significant decrease by 10.2 ± 21.4%, 6.3 ± 5.2%, 11.8 ± 8.6%, and 9.3 ± 2.5% (mean ± SEM, p &lt; .05 for all), respectively. Conclusions CSR may potentially induce neuronal loss and structural changes in the dorsal respiratory nuclei.</description><identifier>ISSN: 0161-8105</identifier><identifier>EISSN: 1550-9109</identifier><identifier>DOI: 10.1093/sleep/zsx072</identifier><identifier>PMID: 28472438</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Animals ; Brain ; Brain Stem - pathology ; Cell Count ; Chronic Disease ; Disease Models, Animal ; Male ; Neurons - pathology ; Rats ; Rats, Sprague-Dawley ; Rodents ; Sleep ; Sleep Deprivation - pathology</subject><ispartof>Sleep (New York, N.Y.), 2017-08, Vol.40 (8)</ispartof><rights>Sleep Research Society 2017. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com. 2017</rights><rights>Sleep Research Society 2017. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com.</rights><rights>Copyright © 2017 Sleep Research Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-90f4ff7b6d820222aec7b3d463e9e9f25bff7a1d5b359c2805500d9e3bb0f41c3</citedby><cites>FETCH-LOGICAL-c455t-90f4ff7b6d820222aec7b3d463e9e9f25bff7a1d5b359c2805500d9e3bb0f41c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,1579,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28472438$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kamali, Ali-Mohammad</creatorcontrib><creatorcontrib>Noorafshan, Ali</creatorcontrib><creatorcontrib>Karimi, Fatemeh</creatorcontrib><creatorcontrib>Karbalay-Doust, Saied</creatorcontrib><creatorcontrib>Nami, Mohammad</creatorcontrib><title>The Impact of Chronic Sleep Restriction on Neuronal Number and Volumetric Correlates of the Dorsal Respiratory Nuclei in a Rat Model</title><title>Sleep (New York, N.Y.)</title><addtitle>Sleep</addtitle><description>Abstract Study Objectives Sleep restriction can result in a range of neurophysiological consequences in the brain including some brain stem nuclei. This study aimed to evaluate the effects of chronic sleep restriction (CSR) on quantitative aspects of brain stem respiratory centers using stereological methods. Methods Male rats were randomly assigned into experimental group (CSR through a modified multiple platform apparatus), corresponding apparatus-control group (grid-floor control) and cage controls. In the grid-floor control group, animals were placed on wire-mesh grids positioned upon CSR apparatus and were then allowed to retain the opportunity to sleep. On day 21, all rats were euthanized with their brains removed for stereological assessments. The nuclei which are known to be involved in respiration rhythm including nucleus tractus solitarius (NTS), parabrachial nuclei (PB), and Kölliker–Fuse nucleus (KF) were evaluated. Results Compared to the control groups, stereological findings in CSR rats revealed a decrease by 5.2 ± 0.01%, 7.1 ± 0.007%, 3.9 ± 0.004%, and 6.3 ± 0.002% (mean ± standard error of the mean [SEM], p &lt; .01 for all) in the volume of NTS, medial PB, lateral PB, and KF nuclei, respectively. Also, the total neuronal number of NTS, medial PB, lateral PB, and KF showed a significant decrease by 10.2 ± 21.4%, 6.3 ± 5.2%, 11.8 ± 8.6%, and 9.3 ± 2.5% (mean ± SEM, p &lt; .05 for all), respectively. 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This study aimed to evaluate the effects of chronic sleep restriction (CSR) on quantitative aspects of brain stem respiratory centers using stereological methods. Methods Male rats were randomly assigned into experimental group (CSR through a modified multiple platform apparatus), corresponding apparatus-control group (grid-floor control) and cage controls. In the grid-floor control group, animals were placed on wire-mesh grids positioned upon CSR apparatus and were then allowed to retain the opportunity to sleep. On day 21, all rats were euthanized with their brains removed for stereological assessments. The nuclei which are known to be involved in respiration rhythm including nucleus tractus solitarius (NTS), parabrachial nuclei (PB), and Kölliker–Fuse nucleus (KF) were evaluated. Results Compared to the control groups, stereological findings in CSR rats revealed a decrease by 5.2 ± 0.01%, 7.1 ± 0.007%, 3.9 ± 0.004%, and 6.3 ± 0.002% (mean ± standard error of the mean [SEM], p &lt; .01 for all) in the volume of NTS, medial PB, lateral PB, and KF nuclei, respectively. Also, the total neuronal number of NTS, medial PB, lateral PB, and KF showed a significant decrease by 10.2 ± 21.4%, 6.3 ± 5.2%, 11.8 ± 8.6%, and 9.3 ± 2.5% (mean ± SEM, p &lt; .05 for all), respectively. Conclusions CSR may potentially induce neuronal loss and structural changes in the dorsal respiratory nuclei.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>28472438</pmid><doi>10.1093/sleep/zsx072</doi><oa>free_for_read</oa></addata></record>
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subjects Animals
Brain
Brain Stem - pathology
Cell Count
Chronic Disease
Disease Models, Animal
Male
Neurons - pathology
Rats
Rats, Sprague-Dawley
Rodents
Sleep
Sleep Deprivation - pathology
title The Impact of Chronic Sleep Restriction on Neuronal Number and Volumetric Correlates of the Dorsal Respiratory Nuclei in a Rat Model
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