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Synthetic torpor: A method for safely and practically transporting experimental animals aboard spaceflight missions to deep space.合成休眠:一种安全实用的方法,可用于在深空飞行任务中安全地运输实验动物。
Life Sci Space Res (Amst). 2018 Feb;16:101-107. doi: 10.1016/j.lssr.2018.01.002. Epub 2018 Jan 12.
2
Involvement of orexin neurons in fasting- and central adenosine-induced hypothermia.食欲素神经元在禁食和中枢腺苷诱导的体温降低中的作用。
Sci Rep. 2018 Feb 9;8(1):2717. doi: 10.1038/s41598-018-21252-w.
3
Modulation of sympathetic vasoconstriction is critical for the effects of sleep on arterial pressure in mice.调节交感血管收缩对于睡眠对小鼠动脉血压的影响至关重要。
J Physiol. 2018 Feb 15;596(4):591-608. doi: 10.1113/JP275353. Epub 2018 Jan 19.
4
Mice Lacking EGR1 Have Impaired Clock Gene (BMAL1) Oscillation, Locomotor Activity, and Body Temperature.缺乏 EGR1 的小鼠表现出时钟基因(BMAL1)振荡、运动活性和体温受损。
J Mol Neurosci. 2018 Jan;64(1):9-19. doi: 10.1007/s12031-017-0996-8. Epub 2017 Nov 14.
5
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Tonic inhibition of brown adipose tissue sympathetic nerve activity via muscarinic acetylcholine receptors in the rostral raphe pallidus.通过罗氏苍白球头部的毒蕈碱型乙酰胆碱受体抑制棕色脂肪组织交感神经活动。
J Physiol. 2017 Dec 15;595(24):7495-7508. doi: 10.1113/JP275299. Epub 2017 Nov 21.
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Striatal adenosine A receptor neurons control active-period sleep via parvalbumin neurons in external globus pallidus.纹状体腺苷 A 受体神经元通过苍白球外侧部的 parvalbumin 神经元控制活跃期睡眠。
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Slow-wave sleep is controlled by a subset of nucleus accumbens core neurons in mice.慢波睡眠由小鼠伏隔核核心神经元的一个子集控制。
Nat Commun. 2017 Sep 29;8(1):734. doi: 10.1038/s41467-017-00781-4.
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New insights on the regulation of the adenine nucleotide pool of erythrocytes in mouse models.小鼠模型中红细胞腺嘌呤核苷酸池调节的新见解。
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Heart rate dynamics in a marsupial hibernator.有袋类冬眠动物的心率动态变化
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腺苷作用是否为非快速动眼睡眠、蛰伏和其他低代谢状态的共同基础?

Is Adenosine Action Common Ground for NREM Sleep, Torpor, and Other Hypometabolic States?

机构信息

Department of Biomedical and Neuromotor Sciences, Alma Mater Studiorum, University of Bologna , Bologna , Italy.

National Institute of Nuclear Physics (INFN), Section of Bologna, Bologna , Italy.

出版信息

Physiology (Bethesda). 2018 May 1;33(3):182-196. doi: 10.1152/physiol.00007.2018.

DOI:10.1152/physiol.00007.2018
PMID:29616880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5966658/
Abstract

This review compares two states that lower energy expenditure: non-rapid eye movement (NREM) sleep and torpor. Knowledge on mechanisms common to these states, and particularly on the role of adenosine in NREM sleep, may ultimately open the possibility of inducing a synthetic torpor-like state in humans for medical applications and long-term space travel. To achieve this goal, it will be important, in perspective, to extend the study to other hypometabolic states, which, unlike torpor, can also be experienced by humans.

摘要

这篇综述比较了两种降低能量消耗的状态

非快速眼动(NREM)睡眠和蛰伏。了解这些状态共有的机制,特别是腺苷在 NREM 睡眠中的作用,最终可能为人类医学应用和长期太空旅行诱导一种类似蛰伏的合成状态开辟可能性。展望未来,为了实现这一目标,将研究扩展到其他代谢率降低的状态将很重要,这些状态与蛰伏不同,人类也可以经历这些状态。