Activation of astrocytes in the dorsomedial hypothalamus accelerates sevoflurane anesthesia emergence in mice.
10.12122/j.issn.1673-4254.2025.04.10
- Author:
Shuting GUO
1
;
Fuyang CAO
1
;
Yongxin GUO
1
;
Yanxiang LI
1
;
Xinyu HAO
1
;
Zhuoning ZHANG
1
;
Zhikang ZHOU
1
;
Li TONG
1
;
Jiangbei CAO
1
Author Information
1. Department of Anesthesia, First Medical Center of Chinese PLA General Hospital, Beijing 100853, China.
- Publication Type:Journal Article
- Keywords:
anesthesia emergence;
astrocytes;
dmh region;
sevoflurane
- MeSH:
Animals;
Astrocytes/physiology*;
Sevoflurane;
Mice, Inbred C57BL;
Mice;
Male;
Electroencephalography;
Anesthetics, Inhalation/pharmacology*;
Hypothalamus/cytology*;
Anesthesia Recovery Period;
Methyl Ethers/pharmacology*
- From:
Journal of Southern Medical University
2025;45(4):751-759
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVES:To investigate the regulatory role of astrocytes in the dorsomedial hypothalamus (DMH) during sevoflurane anesthesia emergence.
METHODS:Forty-two male C57BL/6 mice were randomized into 6 groups (n=7) for assessing astrocyte activation in the dorsomedial hypothalamus (DMH) under sevoflurane anesthesia. Two groups of mice received microinjection of agfaABC1D promoter-driven AAV2 vector into the DMH for GCaMP6 overexpression, and the changes in astrocyte activity during sevoflurane or air inhalation were recorded using calcium imaging. For assessing optogenetic activation of astrocytes, another two groups of mice received microinjection of an optogenetic virus or a control vector into the DMH with optic fiber implantation, and sevoflurane anesthesia emergence was compared using behavioral experiments. In the remaining two groups, electroencephalogram (EEG) recording during sevoflurane anesthesia emergence was conducted after injection of the hChR2-expressing and control vectors. Anesthesia induction and recovery were assessed by observing the righting reflex. EEG data were recorded under 2.0% sevoflurane to calculate the burst suppression ratio (BSR) and under 1.5% sevoflurane for power spectrum analysis. Immunofluorescence staining was performed to visualize the colocalization of GFAP-positive astrocytes with viral protein signals.
RESULTS:Astrocyte activity in the DMH decreased progressively as sevoflurane concentration increased. During 2.0% sevoflurane anesthesia, the mice injected with the ChR2-expressing virus exhibited a significantly shortened wake-up time (P<0.05), and optogenetic activation of the DMH astrocytes led to a marked reduction in BSR (P<0.001). Under 1.5% sevoflurane anesthesia, optogenetic activation resulted in a significant increase in EEG gamma power and a significant decrease in delta power in ChR2 group (P<0.01).
CONCLUSIONS:Optogenetic activation of DMH astrocytes facilitates sevoflurane anesthesia emergence but does not significantly influence anesthesia induction. These findings offer new insights into the mechanisms underlying anesthesia emergence and may provide a potential target for accelerating postoperative recovery and managing anesthesia-related complications.
