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

Q2 Medicine
Theresa E. Bjorness , Robert W. Greene
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引用次数: 5

Abstract

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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急性可卡因对小鼠睡眠/清醒行为的剂量反应
长期使用可卡因与睡眠障碍有关,无论是在积极使用期间,还是在戒断和戒断期间。急性可卡因还会增加非人类受试者的清醒时间,以牺牲慢波睡眠和快速眼动为代价。然而,急性可卡因对小鼠睡眠/清醒活动的影响尚未被研究,由于其高遗传易感性,老鼠是一种通常用于睡眠和成瘾研究的啮齿动物模型。雄性C57BL/6小鼠分别给予三种剂量的可卡因(3.6、9.6、18 mg/kg)和对照,通过多导睡眠描记仪测量其睡眠/清醒活动。可卡因剂量依赖性地增加了睡眠潜伏期,增加了清醒时间,增加了清醒时的快速脑电图活动。清醒的增加主要发生在注射后的第一个小时,随后是反弹的SWS睡眠。睡眠/清醒活动在24小时内正常化。与人类和其他啮齿动物一样,在一种通常用于奖励和成瘾研究的野生型小鼠中,可卡因剂量依赖性地减少了睡眠。
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来源期刊
Neurobiology of Sleep and Circadian Rhythms
Neurobiology of Sleep and Circadian Rhythms Neuroscience-Behavioral Neuroscience
CiteScore
4.50
自引率
0.00%
发文量
9
审稿时长
69 days
期刊介绍: Neurobiology of Sleep and Circadian Rhythms is a multidisciplinary journal for the publication of original research and review articles on basic and translational research into sleep and circadian rhythms. The journal focuses on topics covering the mechanisms of sleep/wake and circadian regulation from molecular to systems level, and on the functional consequences of sleep and circadian disruption. A key aim of the journal is the translation of basic research findings to understand and treat sleep and circadian disorders. Topics include, but are not limited to: Basic and translational research, Molecular mechanisms, Genetics and epigenetics, Inflammation and immunology, Memory and learning, Neurological and neurodegenerative diseases, Neuropsychopharmacology and neuroendocrinology, Behavioral sleep and circadian disorders, Shiftwork, Social jetlag.
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