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去甲肾上腺素缺乏小鼠的睡眠潜伏期和觉醒调节改变。

Altered sleep latency and arousal regulation in mice lacking norepinephrine.

作者信息

Hunsley Melissa S, Palmiter Richard D

机构信息

Howard Hughes Medical Institute and Department of Biochemistry, Box 357370, University of Washington, Seattle, WA 98195-7370, USA.

出版信息

Pharmacol Biochem Behav. 2004 Aug;78(4):765-73. doi: 10.1016/j.pbb.2004.05.008.

Abstract

Latency to sleep and the amount of sensory stimulation required to awaken an animal are measures of arousal threshold, which are ultimately modulated by an arousal regulation system involving many brain areas. Among these brain areas and network connections are wake-promoting nuclei of the brainstem and their corresponding neurotransmitters, including norepinephrine (NE). In this study, we used mice that are unable to produce NE to study its role in regulating sleep latency after a variety of interventions, and to study arousal from sleep after sleep deprivation (SD). Sleep latency was measured after gentle awakening or after injections of saline, caffeine or modafinil. Sleep latency was also measured before and after partial restoration of NE pharmacologically. Arousal threshold was measured by recording the number of decibels of white noise required to wake each mouse from NREM sleep after 0, 3 and 3 + 3 h SD (3 h SD followed by < 2 min sleep, followed by an additional 3 h SD). Results showed that when mice were awakened without being touched, there were no differences in sleep latency between the genotypes. However, after an injection of saline, the control mice increased their sleep latency, whereas the NE-deficient mice did not. There were no group differences in sleep latency after treatment with either stimulant. The sleep latency difference between the genotypes was ameliorated by partial restoration of NE. The arousal threshold experiments revealed that significantly more noise was required to wake the NE-deficient mice after 3 and 3 + 3 h of SD. These findings show that mice lacking NE fall asleep more rapidly only after a mild stressor, such as an intraperitoneal injection. NE-deficient mice are also more difficult to wake up using audio stimulation after SD. The results presented here suggest that NE promotes wakefulness during transitions between sleep and wake under conditions involving mild stress and SD, but not under baseline circumstances.

摘要

入睡潜伏期以及唤醒动物所需的感觉刺激量是觉醒阈值的指标,这些指标最终由涉及多个脑区的觉醒调节系统进行调节。在这些脑区和网络连接中,有脑干的促醒核及其相应的神经递质,包括去甲肾上腺素(NE)。在本研究中,我们使用无法产生NE的小鼠来研究其在各种干预后调节睡眠潜伏期的作用,以及研究睡眠剥夺(SD)后从睡眠中觉醒的情况。在轻柔唤醒后或注射生理盐水、咖啡因或莫达非尼后测量睡眠潜伏期。还在药理学上部分恢复NE前后测量睡眠潜伏期。通过记录在0、3和3 + 3小时SD(3小时SD后接着<2分钟睡眠,然后再进行3小时SD)后将每只小鼠从非快速眼动睡眠中唤醒所需的白噪声分贝数来测量觉醒阈值。结果表明,当小鼠未被触碰就被唤醒时,不同基因型之间的睡眠潜伏期没有差异。然而,注射生理盐水后,对照小鼠的睡眠潜伏期增加,而缺乏NE的小鼠则没有。用任何一种兴奋剂治疗后,各实验组之间的睡眠潜伏期没有差异。通过部分恢复NE改善了不同基因型之间的睡眠潜伏期差异。觉醒阈值实验表明,在3小时和3 + 3小时SD后,唤醒缺乏NE的小鼠需要显著更多的噪声。这些发现表明,仅在轻度应激源(如腹腔注射)后,缺乏NE的小鼠入睡更快。在SD后,使用音频刺激也更难唤醒缺乏NE的小鼠。此处呈现的结果表明,在涉及轻度应激和SD的情况下,NE在睡眠和觉醒转换期间促进觉醒,但在基线情况下则不然。

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