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去甲肾上腺素缺乏的小鼠表现出正常的睡眠-觉醒状态,但在轻度应激和低剂量苯丙胺作用后睡眠潜伏期较短。

Norepinephrine-deficient mice exhibit normal sleep-wake states but have shorter sleep latency after mild stress and low doses of amphetamine.

作者信息

Hunsley Melissa S, Palmiter Richard D

机构信息

Howard Hughes Medical Institute, University of Washington, Seattle 98195-7370, USA.

出版信息

Sleep. 2003 Aug 1;26(5):521-6.

PMID:12938804
Abstract

STUDY OBJECTIVES

Mice lacking the ability to make norepinephrine (NE) were used to investigate how NE may be involved in regulating sleep and sleep latency under normal conditions and as a response to mild stress or varying doses of amphetamine.

DESIGN

Sleep latency was measured in NE-deficient and control mice after behavioral interventions and after 3 low doses of amphetamine. Sleep-wake states were measured using electroencephalography and electromyography for the first 6 hours after lights-on under baseline conditions and after an injection of saline. The first 6 hours after lights-off were also measured under baseline conditions.

SETTING

N/A.

PATIENTS OR PARTICIPANTS

Mice lacking the dopamine beta-hydroxylase gene (Dbh -/-), which is required for NE synthesis, and their littermate controls were used.

INTERVENTIONS

N/A.

MEASUREMENTS AND RESULTS

As measured behaviorally and with electroencephalography, sleep latency was significantly shorter in the NE-deficient mice after cage changing, saline injection, and 3 different doses of amphetamine. There were no differences between the 2 groups in any sleep parameters under baseline conditions or after saline injection during the day or night.

CONCLUSIONS

The NE-deficient mice showed a significantly shorter latency to sleep under many different conditions, measured both behaviorally and with electroencephalography. These data suggest that NE is wake promoting during the period of time between a mildly stressful event or a low dose of amphetamine and sleep onset. The NE-deficient mice did not show deficits in wake or increases in rapid eye movement sleep, as predicted from current models of the involvement of NE in the regulation of these 2 states.

摘要

研究目的

利用缺乏合成去甲肾上腺素(NE)能力的小鼠,研究在正常条件下以及对轻度应激或不同剂量苯丙胺产生反应时,NE 可能如何参与调节睡眠和睡眠潜伏期。

设计

在行为干预后以及给予 3 种低剂量苯丙胺后,测量 NE 缺乏小鼠和对照小鼠的睡眠潜伏期。在基线条件下以及注射生理盐水后,使用脑电图和肌电图测量开灯后头 6 小时的睡眠-觉醒状态。熄灯后头 6 小时也在基线条件下进行测量。

地点

无。

患者或参与者

使用缺乏多巴胺β-羟化酶基因(Dbh -/-)的小鼠及其同窝对照,该基因是 NE 合成所必需的。

干预措施

无。

测量与结果

通过行为学测量和脑电图测量发现,在更换笼子、注射生理盐水以及给予 3 种不同剂量苯丙胺后,NE 缺乏小鼠的睡眠潜伏期明显缩短。在基线条件下或白天和夜间注射生理盐水后,两组在任何睡眠参数上均无差异。

结论

无论是通过行为学测量还是脑电图测量,NE 缺乏小鼠在许多不同条件下的睡眠潜伏期均明显缩短。这些数据表明,在轻度应激事件或低剂量苯丙胺与睡眠开始之间的时间段内,NE 具有促进觉醒的作用。如当前关于 NE 参与这两种状态调节的模型所预测的那样,NE 缺乏小鼠在觉醒方面未表现出缺陷,快速眼动睡眠也未增加。

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