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七氟醚影响老年狨猴和小鼠认知功能的机制:脑小胶质细胞中FKBP5表达上调。

Mechanisms by which sevoflurane affects cognitive function in aged marmosets and mice: up-regulation of FKBP5 expression in brain microglia.

作者信息

Zhang Lei, Zhu Jiao, Miao Zhengjie, Mao Haoli, Jiang Hong

机构信息

Department of Anesthesiology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Department of Anesthesiology, Shandong Provincial Key Medical and Health Laboratory of Anesthesia and Brain Function (The Affiliated Hospital of Qingdao University), The Affiliated Hospital of Qingdao University, Qingdao, Shandong Province, China.

出版信息

Med Gas Res. 2026 Mar 1;16(1):19-25. doi: 10.4103/mgr.MEDGASRES-D-24-00155. Epub 2025 Apr 19.

DOI:10.4103/mgr.MEDGASRES-D-24-00155
PMID:40235085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12318572/
Abstract

JOURNAL/mgres/04.03/01612956-202603000-00004/figure1/v/2025-06-28T140100Z/r/image-tiff Inhalation anesthetics may trigger the hypothalamic-pituitary-adrenal axis. FK-506 binding protein (FKBP5) is a critical regulator of the hypothalamic-pituitary-adrenal axis and has been implicated in postoperative cognitive dysfunction. However, how inhalation anesthetics affect the expression and function of FKBP5 in the brain is unclear. We employed single-nucleus RNA sequencing to delineate the hippocampal transcriptomic profiles of the brains of aged marmosets and mice after sevoflurane anesthesia. The results of single-nucleus RNA sequencing revealed that long-term exposure (6 hours) to sevoflurane significantly increased FKBP5 expression in the hippocampus of aged marmosets and mice, especially in microglia. Western blot assay also verified the above results. The Barnes maze test showed that, compared with heterozygous control mice, microglia-specific FKBP5 conditional knockout mice exhibited improved neurocognitive function after sevoflurane/surgery. Transcriptome sequencing analysis was performed on the brains of microglia-specific FKBP5 conditional knockout mice and heterozygous mice after sevoflurane/surgery and further revealed that FKBP5 was related mainly to inflammatory signaling pathways. Therefore, these findings indicate that long-term exposure to sevoflurane increases FKBP5 expression in the hippocampus of aged marmosets and mice, which thereby affects inflammatory signaling pathways and leads to postoperative cognitive dysfunction.

摘要

《期刊/mgres/04.03/01612956 - 202603000 - 00004/图1/v/2025 - 06 - 28T140100Z/图像 - tiff》吸入麻醉剂可能触发下丘脑 - 垂体 - 肾上腺轴。FK - 506结合蛋白(FKBP5)是下丘脑 - 垂体 - 肾上腺轴的关键调节因子,并且与术后认知功能障碍有关。然而,吸入麻醉剂如何影响大脑中FKBP5的表达和功能尚不清楚。我们采用单核RNA测序来描绘老年狨猴和小鼠在七氟醚麻醉后脑海马的转录组图谱。单核RNA测序结果显示,长期(6小时)暴露于七氟醚显著增加了老年狨猴和小鼠海马中FKBP5的表达,尤其是在小胶质细胞中。蛋白质印迹分析也证实了上述结果。巴恩斯迷宫试验表明,与杂合对照小鼠相比,小胶质细胞特异性FKBP5条件性敲除小鼠在七氟醚/手术后表现出改善的神经认知功能。对七氟醚/手术后的小胶质细胞特异性FKBP5条件性敲除小鼠和杂合小鼠的大脑进行转录组测序分析,进一步揭示FKBP5主要与炎症信号通路有关。因此,这些发现表明,长期暴露于七氟醚会增加老年狨猴和小鼠海马中FKBP5的表达,从而影响炎症信号通路并导致术后认知功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/42640270b094/MGR-16-19-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/1de4337c0d80/MGR-16-19-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/db0f89e11471/MGR-16-19-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/310ee30dcb39/MGR-16-19-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/cd8d60fedd84/MGR-16-19-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/dfb4006993c8/MGR-16-19-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/42640270b094/MGR-16-19-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/1de4337c0d80/MGR-16-19-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/db0f89e11471/MGR-16-19-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/310ee30dcb39/MGR-16-19-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/cd8d60fedd84/MGR-16-19-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/dfb4006993c8/MGR-16-19-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8968/12318572/42640270b094/MGR-16-19-g007.jpg

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FKBP51 is involved in LPS-induced microglial activation via NF-κB signaling to mediate neuroinflammation.FKBP51 通过 NF-κB 信号参与 LPS 诱导的小胶质细胞激活,从而介导神经炎症。
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SKA2 regulated hyperactive secretory autophagy drives neuroinflammation-induced neurodegeneration.
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Cannabidiol alleviates neuroinflammation and attenuates neuropathic pain via targeting FKBP5.大麻二酚通过靶向 FKBP5 减轻神经炎症和神经病理性疼痛。
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