Polysomnographic Features of Sleep Disturbances and REM Sleep Behavior Disorder in the Unilateral 6-OHDA Lesioned Hemiparkinsonian Rat

Sleep pattern disruption, specifically REM sleep behavior disorder (RBD), is a major nonmotor cause of disability in PD. Understanding the pathophysiology of these sleep pattern disturbances is critical to find effective treatments. 24-hour polysomnography (PSG), the gold standard for sleep studies,...

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Main Authors: Quynh Vo, Timothy P. Gilmour, Kala Venkiteswaran, Jidong Fang, Thyagarajan Subramanian
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Parkinson's Disease
Online Access:http://dx.doi.org/10.1155/2014/852965
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author Quynh Vo
Timothy P. Gilmour
Kala Venkiteswaran
Jidong Fang
Thyagarajan Subramanian
author_facet Quynh Vo
Timothy P. Gilmour
Kala Venkiteswaran
Jidong Fang
Thyagarajan Subramanian
author_sort Quynh Vo
collection DOAJ
description Sleep pattern disruption, specifically REM sleep behavior disorder (RBD), is a major nonmotor cause of disability in PD. Understanding the pathophysiology of these sleep pattern disturbances is critical to find effective treatments. 24-hour polysomnography (PSG), the gold standard for sleep studies, has never been used to test sleep dysfunction in the standard 6-OHDA lesioned hemiparkinsonian (HP) rat PD model. In this study, we recorded 24-hour PSG from normal and HP rats. Recordings were scored into wake, rapid eye movement (REM), and non-REM (NREM). We then examined EEG to identify REM periods and EMG to check muscle activity during REM. Normal rats showed higher wakefulness (70–80%) during the dark phase and lower wakefulness (20%) during the light phase. HP rats showed 30–50% sleep in both phases, less modulation and synchronization to the light schedule (P<0.0001), and more long run lengths of wakefulness (P<0.05). HP rats also had more REM epochs with muscle activity than control rats (P<0.05). Our findings that the sleep architecture in the HP rat resembles that of PD patients demonstrate the value of this model in studying the pathophysiological basis of PD sleep disturbances and preclinical therapeutics for PD related sleep disorders including RBD.
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publishDate 2014-01-01
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series Parkinson's Disease
spelling doaj-art-5bd00839e44e46c9b708b6957f02432b2025-02-03T07:25:42ZengWileyParkinson's Disease2090-80832042-00802014-01-01201410.1155/2014/852965852965Polysomnographic Features of Sleep Disturbances and REM Sleep Behavior Disorder in the Unilateral 6-OHDA Lesioned Hemiparkinsonian RatQuynh Vo0Timothy P. Gilmour1Kala Venkiteswaran2Jidong Fang3Thyagarajan Subramanian4Department of Neurology, Penn State College of Medicine, Hershey, PA 17033, USADivision of Engineering, John Brown University, Siloam Springs, AR 72761, USADepartment of Neurology, Penn State College of Medicine, Hershey, PA 17033, USADepartment of Psychiatry, Penn State College of Medicine, Hershey, PA 17033, USADepartment of Neurology, Penn State College of Medicine, Hershey, PA 17033, USASleep pattern disruption, specifically REM sleep behavior disorder (RBD), is a major nonmotor cause of disability in PD. Understanding the pathophysiology of these sleep pattern disturbances is critical to find effective treatments. 24-hour polysomnography (PSG), the gold standard for sleep studies, has never been used to test sleep dysfunction in the standard 6-OHDA lesioned hemiparkinsonian (HP) rat PD model. In this study, we recorded 24-hour PSG from normal and HP rats. Recordings were scored into wake, rapid eye movement (REM), and non-REM (NREM). We then examined EEG to identify REM periods and EMG to check muscle activity during REM. Normal rats showed higher wakefulness (70–80%) during the dark phase and lower wakefulness (20%) during the light phase. HP rats showed 30–50% sleep in both phases, less modulation and synchronization to the light schedule (P<0.0001), and more long run lengths of wakefulness (P<0.05). HP rats also had more REM epochs with muscle activity than control rats (P<0.05). Our findings that the sleep architecture in the HP rat resembles that of PD patients demonstrate the value of this model in studying the pathophysiological basis of PD sleep disturbances and preclinical therapeutics for PD related sleep disorders including RBD.http://dx.doi.org/10.1155/2014/852965
spellingShingle Quynh Vo
Timothy P. Gilmour
Kala Venkiteswaran
Jidong Fang
Thyagarajan Subramanian
Polysomnographic Features of Sleep Disturbances and REM Sleep Behavior Disorder in the Unilateral 6-OHDA Lesioned Hemiparkinsonian Rat
Parkinson's Disease
title Polysomnographic Features of Sleep Disturbances and REM Sleep Behavior Disorder in the Unilateral 6-OHDA Lesioned Hemiparkinsonian Rat
title_full Polysomnographic Features of Sleep Disturbances and REM Sleep Behavior Disorder in the Unilateral 6-OHDA Lesioned Hemiparkinsonian Rat
title_fullStr Polysomnographic Features of Sleep Disturbances and REM Sleep Behavior Disorder in the Unilateral 6-OHDA Lesioned Hemiparkinsonian Rat
title_full_unstemmed Polysomnographic Features of Sleep Disturbances and REM Sleep Behavior Disorder in the Unilateral 6-OHDA Lesioned Hemiparkinsonian Rat
title_short Polysomnographic Features of Sleep Disturbances and REM Sleep Behavior Disorder in the Unilateral 6-OHDA Lesioned Hemiparkinsonian Rat
title_sort polysomnographic features of sleep disturbances and rem sleep behavior disorder in the unilateral 6 ohda lesioned hemiparkinsonian rat
url http://dx.doi.org/10.1155/2014/852965
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