γ-氨基丁酸(GABA)受体激活通过诱导海马脑源性神经营养因子(BDNF)高甲基化,导致小鼠术后认知功能障碍。

GABA receptor activation contributes to post-surgery cognitive impairments in mice by inducing hippocampal BDNF hypermethylation.

作者信息

Wu Tong, Sun Xiao-Yu, Cao Jing, Tong Kun, Hao Jing-Ru, Sun Nan, Gao Can

机构信息

NMPA Key Laboratory for Research and Evaluation of Narcotic and Psychotropic Drugs, Jiangsu Province Key Laboratory of Anesthesiology, Jiangsu Province Key Laboratory of Anesthesia and Analgesia Application, Xuzhou Medical University, Xuzhou, China.

Department of Anesthesia, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.

出版信息

Ann Med. 2025 Dec;57(1):2536221. doi: 10.1080/07853890.2025.2536221. Epub 2025 Jul 22.

Abstract

BACKGROUND

Clinical observations have shown that brain-derived neurotrophic factor (BDNF) expression is reduced in patients with impaired cognitive function after anaesthesia and surgery. Abnormal epigenetic changes may contribute to this condition. The role of the GABAergic system, which is crucial in anaesthetic mechanisms and cognitive function, requires further investigation to determine whether it affects BDNF epigenetic regulation and cognitive outcomes.

MATERIALS AND METHODS

Experiments employed a mouse model perioperative neurocognitive disorder (PND) that comprised laparotomy under isoflurane inhalation anaesthesia. Mice were subjected to behavioural assessments, including the Y-maze and novel object recognition tests for cognitive function and molecular analyses (quantitative polymerase chain reaction, qPCR) and methylation-specific PCR to assess BDNF expression and epigenetic modifications. GABA receptor deactivation was induced by a selective antagonist and changes in BDNF expression and gene methylation were measured.

RESULTS

Aged mice in the PND model had reduced BDNF expression in hippocampal neurons. BDNF protein reduction was linked to increased methylation of the gene, initiated by GABA receptor activation and hyperphosphorylation of downstream signalling proteins. Furthermore, BDNF overexpression experiments demonstrated a partial reversal of cognitive impairment in mice, supporting a causal role for BDNF methylation in PND.

CONCLUSIONS

This study emphasizes the vital interaction between the GABAergic system and the epigenetic control of , shedding light on the mechanisms underlying anaesthesia-related cognitive impairment. Our findings suggest that inhibition of GABA receptor activation to reverse BDNF hypermethylation may represent a potential therapeutic strategy for alleviating PND.

摘要

背景

临床观察表明,麻醉和手术后认知功能受损的患者脑源性神经营养因子(BDNF)表达降低。异常的表观遗传变化可能导致这种情况。在麻醉机制和认知功能中起关键作用的γ-氨基丁酸能系统的作用,需要进一步研究以确定其是否影响BDNF的表观遗传调控和认知结果。

材料与方法

实验采用围手术期神经认知障碍(PND)小鼠模型,该模型包括在异氟烷吸入麻醉下进行剖腹手术。对小鼠进行行为评估,包括用于认知功能的Y迷宫和新物体识别测试,以及分子分析(定量聚合酶链反应,qPCR)和甲基化特异性PCR,以评估BDNF表达和表观遗传修饰。通过选择性拮抗剂诱导GABA受体失活,并测量BDNF表达和基因甲基化的变化。

结果

PND模型中的老年小鼠海马神经元中BDNF表达降低。BDNF蛋白减少与该基因的甲基化增加有关,这是由GABA受体激活和下游信号蛋白的过度磷酸化引发的。此外,BDNF过表达实验证明小鼠认知障碍有部分逆转,支持BDNF甲基化在PND中的因果作用。

结论

本研究强调了γ-氨基丁酸能系统与BDNF表观遗传控制之间的重要相互作用,揭示了麻醉相关认知障碍的潜在机制。我们的研究结果表明,抑制GABA受体激活以逆转BDNF高甲基化可能是减轻PND的一种潜在治疗策略。

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