Suppr超能文献

基底神经节对睡眠-觉醒行为和皮层激活的控制。

Basal ganglia control of sleep-wake behavior and cortical activation.

机构信息

Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.

出版信息

Eur J Neurosci. 2010 Feb;31(3):499-507. doi: 10.1111/j.1460-9568.2009.07062.x. Epub 2010 Jan 25.

Abstract

The basal ganglia (BG) are involved in numerous neurobiological processes that operate on the basis of wakefulness, including motor function, learning, emotion and addictive behaviors. We hypothesized that the BG might play an important role in the regulation of wakefulness. To test this prediction, we made cell body-specific lesions in the striatum and globus pallidus (GP) using ibotenic acid. We found that rats with striatal (caudoputamen) lesions exhibited a 14.95% reduction in wakefulness and robust fragmentation of sleep-wake behavior, i.e. an increased number of state transitions and loss of ultra-long wake bouts (> 120 min). These lesions also resulted in a reduction in the diurnal variation of sleep-wakefulness. On the other hand, lesions of the accumbens core resulted in a 26.72% increase in wakefulness and a reduction in non-rapid eye movement (NREM) sleep bout duration. In addition, rats with accumbens core lesions exhibited excessive digging and scratching. GP lesions also produced a robust increase in wakefulness (45.52%), and frequent sleep-wake transitions and a concomitant decrease in NREM sleep bout duration. Lesions of the subthalamic nucleus or the substantia nigra reticular nucleus produced only minor changes in the amount of sleep-wakefulness and did not alter sleep architecture. Finally, power spectral analysis revealed that lesions of the striatum, accumbens and GP slowed down the cortical electroencephalogram. Collectively, our results suggest that the BG, via a cortico-striato-pallidal loop, are important neural circuitry regulating sleep-wake behaviors and cortical activation.

摘要

基底神经节(BG)参与了许多基于觉醒的神经生物学过程,包括运动功能、学习、情绪和成瘾行为。我们假设 BG 可能在觉醒的调节中发挥重要作用。为了验证这一预测,我们使用异硫氰酸对纹状体和苍白球(GP)进行了细胞体特异性损伤。我们发现,纹状体(尾壳核)损伤的大鼠表现出觉醒减少 14.95%,睡眠-觉醒行为严重碎片化,即状态转换次数增加和超长觉醒期丧失(>120 分钟)。这些损伤还导致睡眠-觉醒的昼夜变化减少。另一方面,伏隔核核心的损伤导致觉醒增加 26.72%,非快速眼动(NREM)睡眠期持续时间减少。此外,伏隔核核心损伤的大鼠表现出过度挖掘和抓挠。GP 损伤也导致觉醒显著增加(45.52%),频繁的睡眠-觉醒转换以及 NREM 睡眠期持续时间相应减少。丘脑底核或黑质网状核的损伤仅导致睡眠-觉醒量的微小变化,并且不改变睡眠结构。最后,功率谱分析表明,纹状体、伏隔核和 GP 的损伤使皮层脑电图减慢。总的来说,我们的结果表明,BG 通过皮质-纹状体-苍白球环路,是调节睡眠-觉醒行为和皮层激活的重要神经回路。

相似文献

1
Basal ganglia control of sleep-wake behavior and cortical activation.基底神经节对睡眠-觉醒行为和皮层激活的控制。
Eur J Neurosci. 2010 Feb;31(3):499-507. doi: 10.1111/j.1460-9568.2009.07062.x. Epub 2010 Jan 25.
5
How do the basal ganglia regulate sleep-wake behavior?基底神经节如何调节睡眠-觉醒行为?
Trends Neurosci. 2012 Dec;35(12):723-32. doi: 10.1016/j.tins.2012.07.001. Epub 2012 Aug 1.
8
Role of the basal ganglia in the control of sleep and wakefulness.基底神经节在睡眠和清醒控制中的作用。
Curr Opin Neurobiol. 2013 Oct;23(5):780-5. doi: 10.1016/j.conb.2013.02.001. Epub 2013 Apr 24.

引用本文的文献

本文引用的文献

2
Seven problems on the basal ganglia.基底神经节的七个问题。
Curr Opin Neurobiol. 2008 Dec;18(6):595-604. doi: 10.1016/j.conb.2008.11.001. Epub 2008 Dec 8.
6
A putative flip-flop switch for control of REM sleep.一种用于控制快速眼动睡眠的假定触发器开关。
Nature. 2006 Jun 1;441(7093):589-94. doi: 10.1038/nature04767. Epub 2006 May 10.
8
Insomnia following hypocretin2-saporin lesions of the substantia nigra.黑质中促食欲素2-皂草素损伤后的失眠。
Neuroscience. 2006;137(1):29-36. doi: 10.1016/j.neuroscience.2005.08.088. Epub 2005 Nov 11.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验