Sevoflurane depresses neurons in the medial parabrachial nucleus by potentiating postsynaptic GABAA receptors and background potassium channels. (15th December 2020)

• Record Type: Journal Article
• Authors: Xu, Wei; Wang, Lu; Yuan, Xiang-Shan; Wang, Tian-Xiao; Li, Wen-Xian; Qu, Wei-Min; Hong, Zong-Yuan; Huang, Zhi-Li
• Is Part Of: Neuropharmacology. Volume 181(2020)
• Publication Date: 2020-12-15
• Subjects: Sevoflurane -- GABAA receptors -- Potassium channels -- Medial parabrachial nucleus; Neuropsychopharmacology -- Periodicals; Autonomic Agents -- Periodicals; Neuropsychopharmacologie -- Périodiques; Neuropsychopharmacology; Periodicals; Electronic journals; 615.78
• DOI: 10.1016/j.neuropharm.2020.108249
• Languages: English
• ISSNs: 0028-3908

Abstract

Abstract: Despite persistent clinical use for over 170 years, the neuronal mechanisms by which general anesthetics produce hypnosis remain unclear. Previous studies suggest that anesthetics exert hypnotic effects by acting on endogenous arousal circuits. Recently, it has been shown that the medial parabrachial nucleus (MPB) is a novel wake-promoting component in the dorsolateral pons. However, it is not known whether and how the MPB contributes to anesthetic-induced hypnosis. Here, we investigated the action of sevoflurane, a widely used volatile anesthetic agent that best represents the drug class of halogenated ethers, on MPB neurons in mice. Using in vivo fiber photometry, we found that the population activities of MPB neurons were inhibited during sevoflurane-induced loss of consciousness. Using in vitro whole-cell patch-clamp recordings, we revealed that sevoflurane suppressed the firing rate of MPB neurons in concentration-dependent and reversible manners. At a concentration equal to MAC of hypnosis, sevoflurane potentiated synaptic GABAA receptors (GABAA -Rs), and the inhibitory effect of sevoflurane on the firing rate of MPB neurons was completely abolished by picrotoxin, which is a selective GABAA -R antagonist. At a concentration equivalent to MAC of immobility, sevoflurane directly hyperpolarized MPB neurons and induced a significant decrease in membrane input resistance by increasing a basal potassium conductance. Moreover, pharmacological blockade of GABAA -Rs in the MPB prolongs induction and shortens emergence under sevoflurane inhalation at MAC of hypnosis. These results indicate that sevoflurane inhibits MPB neurons through postsynaptic GABAA -Rs and background potassium channels, which contributes to sevoflurane-induced hypnosis. Highlights: Population activities of MPB neurons decrease before the onset of sevoflurane-induced LOC. Sevoflurane suppresses the firing rate of MPB neurons in acute pons slices. Sevoflurane at MAC of hypnosis inhibits MPB neurons through postsynaptic GABAA Rs. Sevoflurane at MAC of immobility inhibits MPB neurons through background K + channels.