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) |
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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 |
format | Article |
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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.</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 < .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.</description><subject>Animals</subject><subject>Brain</subject><subject>Brain Stem - pathology</subject><subject>Cell Count</subject><subject>Chronic Disease</subject><subject>Disease Models, Animal</subject><subject>Male</subject><subject>Neurons - pathology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rodents</subject><subject>Sleep</subject><subject>Sleep Deprivation - pathology</subject><issn>0161-8105</issn><issn>1550-9109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kU1LxDAQhoMouq7ePEvAgx6sm6RNtznK-gm6gl_XkqZTrKRNTVpQz_5wZ1314EEIhDDPPMPkJWSHsyPOVDwJFqCbvIdXNhUrZMSlZJHCyioZMZ7yKONMbpDNEJ4ZvhMVr5MNkSVTkcTZiHzcPwG9bDpteuoqOnvyrq0NvVtI6S2E3temr11L8cxhwKq2dD40BXiq25I-Ojs0sKDozHkPVvcQFqYevSfOB8RR09Ve986_YauxUNO6pZre6p5euxLsFlmrtA2w_X2PycPZ6f3sIrq6Ob-cHV9FJpGyjxSrkqqaFmmZCSaE0GCmRVwmaQwKVCVkgVXNS1nEUhmRMfwKViqIiwI7uYnH5GDp7bx7GXC5vKmDAWt1C24IOc9UyhLBJUN07w_67AaPyyOlUqUyrnDumBwuKeNdCB6qvPN1o_1bzlm-SCf_SidfpoP47rd0KBoof-GfOBDYXwJu6P5XfQK0p5rs</recordid><startdate>20170801</startdate><enddate>20170801</enddate><creator>Kamali, Ali-Mohammad</creator><creator>Noorafshan, Ali</creator><creator>Karimi, Fatemeh</creator><creator>Karbalay-Doust, Saied</creator><creator>Nami, Mohammad</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20170801</creationdate><title>The Impact of Chronic Sleep Restriction on Neuronal Number and Volumetric Correlates of the Dorsal Respiratory Nuclei in a Rat Model</title><author>Kamali, Ali-Mohammad ; Noorafshan, Ali ; Karimi, Fatemeh ; Karbalay-Doust, Saied ; Nami, Mohammad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-90f4ff7b6d820222aec7b3d463e9e9f25bff7a1d5b359c2805500d9e3bb0f41c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Brain</topic><topic>Brain Stem - pathology</topic><topic>Cell Count</topic><topic>Chronic Disease</topic><topic>Disease Models, Animal</topic><topic>Male</topic><topic>Neurons - pathology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rodents</topic><topic>Sleep</topic><topic>Sleep Deprivation - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kamali, Ali-Mohammad</creatorcontrib><creatorcontrib>Noorafshan, Ali</creatorcontrib><creatorcontrib>Karimi, Fatemeh</creatorcontrib><creatorcontrib>Karbalay-Doust, Saied</creatorcontrib><creatorcontrib>Nami, Mohammad</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Sleep (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kamali, Ali-Mohammad</au><au>Noorafshan, Ali</au><au>Karimi, Fatemeh</au><au>Karbalay-Doust, Saied</au><au>Nami, Mohammad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Impact of Chronic Sleep Restriction on Neuronal Number and Volumetric Correlates of the Dorsal Respiratory Nuclei in a Rat Model</atitle><jtitle>Sleep (New York, N.Y.)</jtitle><addtitle>Sleep</addtitle><date>2017-08-01</date><risdate>2017</risdate><volume>40</volume><issue>8</issue><issn>0161-8105</issn><eissn>1550-9109</eissn><abstract>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.</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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