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Dose response of acute cocaine on sleep/waking behavior in mice

Chronic cocaine use has been associated with sleep disturbances, both during active use periods and during withdrawal and abstinence. Acute cocaine also increases waking at the expense of slow wave sleep and Rapid Eye Movement in non-human subjects. However, the effects of acute cocaine on sleep/wak...

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Autores principales: Bjorness, Theresa E., Greene, Robert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584645/
https://www.ncbi.nlm.nih.gov/pubmed/31236515
http://dx.doi.org/10.1016/j.nbscr.2018.02.001
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author Bjorness, Theresa E.
Greene, Robert W.
author_facet Bjorness, Theresa E.
Greene, Robert W.
author_sort Bjorness, Theresa E.
collection PubMed
description Chronic cocaine use has been associated with sleep disturbances, both during active use periods and during withdrawal and abstinence. Acute cocaine also increases waking at the expense of slow wave sleep and Rapid Eye Movement in non-human subjects. However, the effects of acute cocaine on sleep/waking activity in mice, a rodent model commonly used in both sleep and addiction research due to its high genetic tractability, has yet to be investigated. Sleep/waking activity was measured via polysomnography following IP administration of three doses of cocaine (3.6, 9.6, 18 mg/kg) and vehicle control in male C57BL/6 mice. Cocaine dose-dependently increased sleep latency, increased waking time and increased fast EEG activity within waking. Increases in waking occurred primarily during the first hour following injection, followed by rebound SWS sleep. Sleep/waking activity normalized within a 24-hour period. As with humans and other rodents, cocaine dose dependently reduces sleep in a wildtype strain of mice commonly used in reward and addiction research.
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spelling pubmed-65846452019-06-24 Dose response of acute cocaine on sleep/waking behavior in mice Bjorness, Theresa E. Greene, Robert W. Neurobiol Sleep Circadian Rhythms Research Paper Chronic cocaine use has been associated with sleep disturbances, both during active use periods and during withdrawal and abstinence. Acute cocaine also increases waking at the expense of slow wave sleep and Rapid Eye Movement in non-human subjects. However, the effects of acute cocaine on sleep/waking activity in mice, a rodent model commonly used in both sleep and addiction research due to its high genetic tractability, has yet to be investigated. Sleep/waking activity was measured via polysomnography following IP administration of three doses of cocaine (3.6, 9.6, 18 mg/kg) and vehicle control in male C57BL/6 mice. Cocaine dose-dependently increased sleep latency, increased waking time and increased fast EEG activity within waking. Increases in waking occurred primarily during the first hour following injection, followed by rebound SWS sleep. Sleep/waking activity normalized within a 24-hour period. As with humans and other rodents, cocaine dose dependently reduces sleep in a wildtype strain of mice commonly used in reward and addiction research. Elsevier 2018-02-24 /pmc/articles/PMC6584645/ /pubmed/31236515 http://dx.doi.org/10.1016/j.nbscr.2018.02.001 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Bjorness, Theresa E.
Greene, Robert W.
Dose response of acute cocaine on sleep/waking behavior in mice
title Dose response of acute cocaine on sleep/waking behavior in mice
title_full Dose response of acute cocaine on sleep/waking behavior in mice
title_fullStr Dose response of acute cocaine on sleep/waking behavior in mice
title_full_unstemmed Dose response of acute cocaine on sleep/waking behavior in mice
title_short Dose response of acute cocaine on sleep/waking behavior in mice
title_sort dose response of acute cocaine on sleep/waking behavior in mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584645/
https://www.ncbi.nlm.nih.gov/pubmed/31236515
http://dx.doi.org/10.1016/j.nbscr.2018.02.001
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