神经元有助于重新启动咪达唑仑导致的昏迷。

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2024-11-20 DOI:10.7554/eLife.97954
LeYuan Gu, WeiHui Shao, Lu Liu, Qing Xu, YuLing Wang, JiaXuan Gu, Yue Yang, ZhuoYue Zhang, YaXuan Wu, Yue Shen, Qian Yu, XiTing Lian, HaiXiang Ma, YuanLi Zhang, HongHai Zhang
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引用次数: 0

摘要

咪达唑仑的出现对现代临床实践有着深远的影响。咪达唑仑的催眠和镇静作用使其具有广泛的临床适用性。然而,咪达唑仑调节意识改变的具体机制仍未确定。本研究利用药理学、光遗传学、化学遗传学、纤维光度计和基因敲除等方法,在体内揭示了小脑-视前核外侧去甲肾上腺素能神经回路在调节咪达唑仑诱导的意识改变中的作用。这种效应是由α1肾上腺素能受体介导的。此外,γ-氨基丁酸受体A型(GABAA-R)是咪达唑仑在LC中的一个关键结合位点。这些发现将为研究咪达唑仑用药后意识恢复的神经回路机制提供新的视角,有助于指导临床用药的时机,并提出有效的干预目标,以便及时从咪达唑仑引起的意识丧失中恢复过来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NE contribution to rebooting unconsciousness caused by midazolam.

The advent of midazolam holds profound implications for modern clinical practice. The hypnotic and sedative effects of midazolam afford it broad clinical applicability. However, the specific mechanisms underlying the modulation of altered consciousness by midazolam remain elusive. Herein, using pharmacology, optogenetics, chemogenetics, fiber photometry, and gene knockdown, this in vivo research revealed the role of locus coeruleus (LC)-ventrolateral preoptic nucleus noradrenergic neural circuit in regulating midazolam-induced altered consciousness. This effect was mediated by α1 adrenergic receptors. Moreover, gamma-aminobutyric acid receptor type A (GABAA-R) represents a mechanistically crucial binding site in the LC for midazolam. These findings will provide novel insights into the neural circuit mechanisms underlying the recovery of consciousness after midazolam administration and will help guide the timing of clinical dosing and propose effective intervention targets for timely recovery from midazolam-induced loss of consciousness.

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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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