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地西泮对小鼠睡眠时局部皮质神经活动的影响。

Diazepam effects on local cortical neural activity during sleep in mice.

机构信息

Department of Physiology, Anatomy and Genetics, University of Oxford/Sleep and Circadian Neuroscience Institute, United Kingdom.

Department of Physiology, Anatomy and Genetics, University of Oxford/Sleep and Circadian Neuroscience Institute, United Kingdom.

出版信息

Biochem Pharmacol. 2021 Sep;191:114515. doi: 10.1016/j.bcp.2021.114515. Epub 2021 Mar 10.

Abstract

GABA-ergic neurotransmission plays a key role in sleep regulatory mechanisms and in brain oscillations during sleep. Benzodiazepines such as diazepam are known to induce sedation and promote sleep, however, EEG spectral power in slow frequencies is typically reduced after the administration of benzodiazepines or similar compounds. EEG slow waves arise from a synchronous alternation between periods of cortical network activity (ON) and silence (OFF), and represent a sensitive marker of preceding sleep-wake history. Yet it remains unclear how benzodiazepines act on cortical neural activity during sleep. To address this, we obtained chronic recordings of local field potentials and multiunit activity (MUA) from deep cortical layers of the primary motor cortex in freely behaving mice after diazepam injection. We found that the amplitude of individual LFP slow waves was significantly reduced after diazepam injection and was accompanied by a lower incidence and duration of the corresponding neuronal OFF periods. Further investigation suggested that this is due to a disruption in the synchronisation of cortical neurons. Our data suggest that the state of global sleep and local cortical synchrony can be dissociated, and that the brain state induced by benzodiazepines is qualitatively different from spontaneous physiological sleep.

摘要

GABA 能神经传递在睡眠调节机制和睡眠期间的脑振荡中起着关键作用。众所周知,苯二氮䓬类药物如地西泮具有镇静和促进睡眠的作用,然而,在给予苯二氮䓬类药物或类似化合物后,脑电图慢波频率的功率通常会降低。脑电图慢波源自皮质网络活动(ON)和沉默(OFF)期间的同步交替,并且是先前睡眠-觉醒历史的敏感标志物。然而,苯二氮䓬类药物如何在睡眠期间作用于皮质神经活动仍不清楚。为了解决这个问题,我们在自由活动的小鼠的初级运动皮层的深层皮质层中获得了地西泮注射后的局部场电位和多单位活动(MUA)的慢性记录。我们发现,地西泮注射后单个 LFP 慢波的幅度显着降低,并且伴随着相应神经元 OFF 期的发生率和持续时间降低。进一步的研究表明,这是由于皮质神经元同步性的破坏。我们的数据表明,全局睡眠状态和局部皮质同步性可以分离,并且苯二氮䓬类药物诱导的脑状态与自发生理睡眠在性质上不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4407/8363939/25de8909728f/ga1.jpg

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