Orexin signalling in the nucleus accumbens promotes arousal from isoflurane anaesthesia and restores communication between the nucleus accumbens and frontal cortex.

IF 9.2 1区 医学 Q1 ANESTHESIOLOGY
Jia Huo, Huiming Li, Dan Wang, Sa Wang, Xinxin Zhang, Hailong Dong, Jiannan Li
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引用次数: 0

Abstract

Background: Orexin can induce arousal from general anaesthesia; however, the underlying mechanisms are not fully understood. Nucleus accumbens (NAc), a downstream target of orexinergic neurones, plays a role in regulating consciousness. We aimed to clarify whether and how the NAc mediates the arousal effects of orexin.

Methods: Fibre photometry was used to track changes of orexinergic afferent activity during isoflurane anaesthesia and arousal from anaesthesia. Optogenetics was used to study the effects of orexinergic afferents to the NAc. Neuropharmacology approaches were used to assess receptor mechanisms. Optogenetics and in vivo electrophysiology were used to assess the influence of orexin on NAc neuronal firing and communication between the NAc and the frontal cortex.

Results: Orexinergic afferents in the NAc were wake-active during isoflurane anaesthesia and the arousal process. Optogenetic activation of orexinergic terminals in the NAc prolonged the time to induction, shortened time to emergence, and reduced the burst suppression ratio (from 67.4% [2.5%] to 14.5% [1.0%]; n=6, P<0.001) during 1.4 vol% isoflurane anaesthesia. Microinjection of orexin-A into the NAc promoted arousal from isoflurane anaesthesia. Orexin-1 receptors were primarily expressed in NAc D1 receptor-positive (D1R+) neurones. Optogenetic activation of orexinergic terminals increased D1R+ neuronal firing (from 0.77 [0.54] spikes s-1 to 2.53 [0.46] spikes s-1; n=24, P=0.0194) and restored NAc-to-frontal cortex coherence during isoflurane anaesthesia.

Conclusions: Orexin restores communication between the NAc and frontal cortex by upregulating the activity of D1R+ neurones, thereby promoting arousal from isoflurane anaesthesia.

伏隔核中的食欲素信号促进异氟醚麻醉后的觉醒,并恢复伏隔核与额叶皮质之间的通信。
背景:食欲素可诱导全麻唤醒;然而,其潜在机制尚未完全了解。伏隔核(NAc)是食欲能神经元的下游靶点,在调节意识中起着重要作用。我们的目的是澄清NAc是否以及如何介导食欲素的唤醒作用。方法:采用纤维光度法,观察异氟醚麻醉和醒觉过程中食欲能传入活动的变化。利用光遗传学方法研究了促食能传入对NAc的影响。神经药理学方法用于评估受体机制。采用光遗传学和体内电生理学方法评估食欲素对NAc神经元放电和NAc与额叶皮质间通讯的影响。结果:在异氟醚麻醉和觉醒过程中,NAc的食欲能事件具有清醒活性。光遗传激活NAc的促食能末端延长了诱导时间,缩短了萌发时间,使突发抑制率从67.4%[2.5%]降低到14.5% [1.0%];n=6, P+)个神经元。光遗传激活可使D1R+神经元放电从0.77[0.54]个s-1峰增加到2.53[0.46]个s-1峰;n=24, P=0.0194),异氟醚麻醉期间nac -额叶皮质一致性恢复。结论:Orexin通过上调D1R+神经元的活性,恢复NAc与额叶皮质之间的通讯,从而促进异氟醚麻醉后的觉醒。
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来源期刊
CiteScore
13.50
自引率
7.10%
发文量
488
审稿时长
27 days
期刊介绍: The British Journal of Anaesthesia (BJA) is a prestigious publication that covers a wide range of topics in anaesthesia, critical care medicine, pain medicine, and perioperative medicine. It aims to disseminate high-impact original research, spanning fundamental, translational, and clinical sciences, as well as clinical practice, technology, education, and training. Additionally, the journal features review articles, notable case reports, correspondence, and special articles that appeal to a broader audience. The BJA is proudly associated with The Royal College of Anaesthetists, The College of Anaesthesiologists of Ireland, and The Hong Kong College of Anaesthesiologists. This partnership provides members of these esteemed institutions with access to not only the BJA but also its sister publication, BJA Education. It is essential to note that both journals maintain their editorial independence. Overall, the BJA offers a diverse and comprehensive platform for anaesthetists, critical care physicians, pain specialists, and perioperative medicine practitioners to contribute and stay updated with the latest advancements in their respective fields.
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