Subunit-specific mechanisms of isoflurane-induced acute tonic inhibition in dentate gyrus granule neuron.

IF 2.8 4区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Experimental Biology and Medicine Pub Date : 2024-10-28 eCollection Date: 2024-01-01 DOI:10.3389/ebm.2024.10171
Zhiqiang Yu, Xiaodan Chen, Zheng Liu, Ran Ding, Jin Xu
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Abstract

Prolonged exposure to volatile anesthetics may raise the risk of developing cognitive impairment by acting on gamma-a Aminobutyric acid A receptors (GABAAR). The dentate gyrus plays an important role in the hippocampus and has a high potential for neural plasticity. However, it is unknown whether prolonged anesthesia induces a change in acute phasic or tonic inhibition in dentate gyrus granule cells (DGGCs) by acting on GABAAR. In order to verify the effects of volatile anesthetics on the current in DGGCs, a whole-cell patch was applied to record acute brain slices, and this study indicated that 4 h but not 2 h of isoflurane (ISO) exposure induced significantly larger tonic currents in DGGCs other than hippocampal CA1 pyramidal and thalamic relay neurons. Furthermore, this study demonstrated that the increased tonic current in DGGCs was dependent on the δ subunit-containing GABAARs by using transgenic δ subunit knockout mice. In conclusion, the δ subunit specific GABAAR is the key element that increased acute tonic inhibition in DGGCs of mice after prolonged ISO exposure, which may be one of the mechanisms of ISO neurotoxicity to the developing brain.

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异氟烷诱导齿状回颗粒神经元急性强直性抑制的亚单位特异性机制
长期接触挥发性麻醉剂可能会通过作用于γ-a氨基丁酸A受体(GABAAR)而增加认知障碍的发病风险。齿状回在海马中扮演着重要角色,具有很高的神经可塑性。然而,长期麻醉是否会通过作用于 GABAAR 而诱导齿状回颗粒细胞(DGGCs)的急性阶段性或强直性抑制发生变化,目前尚不清楚。为了验证挥发性麻醉剂对DGGCs电流的影响,研究人员使用全细胞贴片记录急性脑切片,结果表明,异氟醚(ISO)暴露4小时而非2小时可诱导海马CA1锥体和丘脑中继神经元以外的DGGCs产生明显较大的强直电流。此外,本研究还利用转基因δ亚基敲除小鼠证明,DGGCs 强直电流的增加依赖于含δ亚基的 GABAARs。总之,δ亚基特异性 GABAAR 是长时间暴露于 ISO 后增加小鼠 DGGCs 急性强直抑制的关键因素,这可能是 ISO 对发育中大脑神经毒性的机制之一。
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来源期刊
Experimental Biology and Medicine
Experimental Biology and Medicine 医学-医学:研究与实验
CiteScore
6.00
自引率
0.00%
发文量
157
审稿时长
1 months
期刊介绍: Experimental Biology and Medicine (EBM) is a global, peer-reviewed journal dedicated to the publication of multidisciplinary and interdisciplinary research in the biomedical sciences. EBM provides both research and review articles as well as meeting symposia and brief communications. Articles in EBM represent cutting edge research at the overlapping junctions of the biological, physical and engineering sciences that impact upon the health and welfare of the world''s population. Topics covered in EBM include: Anatomy/Pathology; Biochemistry and Molecular Biology; Bioimaging; Biomedical Engineering; Bionanoscience; Cell and Developmental Biology; Endocrinology and Nutrition; Environmental Health/Biomarkers/Precision Medicine; Genomics, Proteomics, and Bioinformatics; Immunology/Microbiology/Virology; Mechanisms of Aging; Neuroscience; Pharmacology and Toxicology; Physiology; Stem Cell Biology; Structural Biology; Systems Biology and Microphysiological Systems; and Translational Research.
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