Nitric oxide mediated recovery sleep is attenuated with aging

Abstract Nitric oxide (NO) produced by inducible nitric oxide synthase (iNOS) in the cholinergic basal forebrain (BF) during sleep deprivation (SD) is implicated in adenosine (AD) release and induction of recovery sleep. Aging is associated with impairments in sleep homeostasis, such as decrease in...

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Veröffentlicht in:Neurobiology of aging 2010-11, Vol.31 (11), p.2011-2019
Hauptverfasser: Rytkönen, Kirsi-Marja, Wigren, Henna-Kaisa, Kostin, Andrey, Porkka-Heiskanen, Tarja, Kalinchuk, Anna V
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container_end_page 2019
container_issue 11
container_start_page 2011
container_title Neurobiology of aging
container_volume 31
creator Rytkönen, Kirsi-Marja
Wigren, Henna-Kaisa
Kostin, Andrey
Porkka-Heiskanen, Tarja
Kalinchuk, Anna V
description Abstract Nitric oxide (NO) produced by inducible nitric oxide synthase (iNOS) in the cholinergic basal forebrain (BF) during sleep deprivation (SD) is implicated in adenosine (AD) release and induction of recovery sleep. Aging is associated with impairments in sleep homeostasis, such as decrease in non-rapid eye movement sleep (NREM) intensity following SD. We hypothesized that age related changes in sleep homeostasis may be induced by impairments in NO-mediated sleep induction. To test this hypothesis we measured levels of NO and iNOS in the BF during SD as well as recovery sleep after SD and NO-donor (DETA/NO) infusion into the BF in three age groups of rats (young, 4 months; middle-aged, 14 months; old, 24 months). We found that in aged rats as compared to young (1) recovery NREM sleep intensity was significantly decreased, (2) neither iNOS nor NO increased in the BF during SD, and (3) DETA/NO infusion failed to induce sleep. Together, these results support our hypothesis that aging impairs the mechanism through which NO in the BF induces sleep.
doi_str_mv 10.1016/j.neurobiolaging.2008.10.006
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Aging is associated with impairments in sleep homeostasis, such as decrease in non-rapid eye movement sleep (NREM) intensity following SD. We hypothesized that age related changes in sleep homeostasis may be induced by impairments in NO-mediated sleep induction. To test this hypothesis we measured levels of NO and iNOS in the BF during SD as well as recovery sleep after SD and NO-donor (DETA/NO) infusion into the BF in three age groups of rats (young, 4 months; middle-aged, 14 months; old, 24 months). We found that in aged rats as compared to young (1) recovery NREM sleep intensity was significantly decreased, (2) neither iNOS nor NO increased in the BF during SD, and (3) DETA/NO infusion failed to induce sleep. 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Psychology</subject><subject>Inducible nitric oxide</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Microdialysis</subject><subject>Neurology</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Prosencephalon - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Sleep</subject><subject>Sleep - physiology</subject><subject>Sleep deprivation</subject><subject>Sleep Deprivation - metabolism</subject><subject>Sleep homeostasis</subject><subject>Sleep Stages - physiology</subject><subject>Sleep. 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Vigilance</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rytkönen, Kirsi-Marja</creatorcontrib><creatorcontrib>Wigren, Henna-Kaisa</creatorcontrib><creatorcontrib>Kostin, Andrey</creatorcontrib><creatorcontrib>Porkka-Heiskanen, Tarja</creatorcontrib><creatorcontrib>Kalinchuk, Anna V</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Neurobiology of aging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rytkönen, Kirsi-Marja</au><au>Wigren, Henna-Kaisa</au><au>Kostin, Andrey</au><au>Porkka-Heiskanen, Tarja</au><au>Kalinchuk, Anna V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitric oxide mediated recovery sleep is attenuated with aging</atitle><jtitle>Neurobiology of aging</jtitle><addtitle>Neurobiol Aging</addtitle><date>2010-11-01</date><risdate>2010</risdate><volume>31</volume><issue>11</issue><spage>2011</spage><epage>2019</epage><pages>2011-2019</pages><issn>0197-4580</issn><eissn>1558-1497</eissn><coden>NEAGDO</coden><abstract>Abstract Nitric oxide (NO) produced by inducible nitric oxide synthase (iNOS) in the cholinergic basal forebrain (BF) during sleep deprivation (SD) is implicated in adenosine (AD) release and induction of recovery sleep. 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subjects Adenosine
Aging
Aging - physiology
Animals
Biological and medical sciences
Development. Senescence. Regeneration. Transplantation
Fundamental and applied biological sciences. Psychology
Inducible nitric oxide
Internal Medicine
Male
Microdialysis
Neurology
Nitric oxide
Nitric Oxide - metabolism
Nitric Oxide Synthase Type II - metabolism
Prosencephalon - metabolism
Rats
Rats, Wistar
Sleep
Sleep - physiology
Sleep deprivation
Sleep Deprivation - metabolism
Sleep homeostasis
Sleep Stages - physiology
Sleep. Vigilance
Vertebrates: nervous system and sense organs
title Nitric oxide mediated recovery sleep is attenuated with aging
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