Yuan Li, Haifeng Duan, Qi Wang, Yi Lin, Zhoujing Yang, Zhiru Wang, Yingwei Wang, Kai Wei, Daojie Xu
{"title":"抑制Rac1减轻异丙酚诱导的发育小鼠海马齿状回神经毒性。","authors":"Yuan Li, Haifeng Duan, Qi Wang, Yi Lin, Zhoujing Yang, Zhiru Wang, Yingwei Wang, Kai Wei, Daojie Xu","doi":"10.1007/s11064-025-04462-3","DOIUrl":null,"url":null,"abstract":"<p><p>Accumulating evidence from animals has shown that multiple exposures to general anesthetics during brain development may cause extensive neuronal apoptosis and long-term memory impairments. However, the underlying mechanism is still poorly understood. In the present study, C57BL/6 mice were administered with propofol at postnatal days 19-21. We found that propofol exposure significantly increased neuronal apoptosis in the mouse hippocampal dentate gyrus, as evidenced by cleaved caspase-3 immunofluorescence. Additionally, propofol exposure increased the activation and expression of Ras-related C3 botulinum toxin substrate 1 (Rac1) in the dentate gyrus, as shown by western blotting. Modulating Rac1, either through inhibition or overexpression, was found to mitigate or exacerbate propofol-induced neuronal apoptosis, respectively. We further demonstrated that propofol decreased the expression of the anti-apoptotic protein phosphorylated serine/threonine kinase Akt via Rac1. The results of the open field and Morris water maze test further revealed that silencing Rac1 alleviated propofol-induced cognitive dysfunction. Our findings demonstrated that propofol exposure induced neuronal apoptosis and long-term cognitive dysfunction in the mouse hippocampal dentate gyrus by regulating Rac1.</p>","PeriodicalId":719,"journal":{"name":"Neurochemical Research","volume":"50 4","pages":"207"},"PeriodicalIF":3.8000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Inhibition of Rac1 Attenuated Propofol-Induced Neurotoxicity in the Hippocampal Dentate Gyrus in Developing Mice.\",\"authors\":\"Yuan Li, Haifeng Duan, Qi Wang, Yi Lin, Zhoujing Yang, Zhiru Wang, Yingwei Wang, Kai Wei, Daojie Xu\",\"doi\":\"10.1007/s11064-025-04462-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Accumulating evidence from animals has shown that multiple exposures to general anesthetics during brain development may cause extensive neuronal apoptosis and long-term memory impairments. However, the underlying mechanism is still poorly understood. In the present study, C57BL/6 mice were administered with propofol at postnatal days 19-21. We found that propofol exposure significantly increased neuronal apoptosis in the mouse hippocampal dentate gyrus, as evidenced by cleaved caspase-3 immunofluorescence. Additionally, propofol exposure increased the activation and expression of Ras-related C3 botulinum toxin substrate 1 (Rac1) in the dentate gyrus, as shown by western blotting. Modulating Rac1, either through inhibition or overexpression, was found to mitigate or exacerbate propofol-induced neuronal apoptosis, respectively. We further demonstrated that propofol decreased the expression of the anti-apoptotic protein phosphorylated serine/threonine kinase Akt via Rac1. The results of the open field and Morris water maze test further revealed that silencing Rac1 alleviated propofol-induced cognitive dysfunction. Our findings demonstrated that propofol exposure induced neuronal apoptosis and long-term cognitive dysfunction in the mouse hippocampal dentate gyrus by regulating Rac1.</p>\",\"PeriodicalId\":719,\"journal\":{\"name\":\"Neurochemical Research\",\"volume\":\"50 4\",\"pages\":\"207\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-06-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neurochemical Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s11064-025-04462-3\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurochemical Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11064-025-04462-3","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Inhibition of Rac1 Attenuated Propofol-Induced Neurotoxicity in the Hippocampal Dentate Gyrus in Developing Mice.
Accumulating evidence from animals has shown that multiple exposures to general anesthetics during brain development may cause extensive neuronal apoptosis and long-term memory impairments. However, the underlying mechanism is still poorly understood. In the present study, C57BL/6 mice were administered with propofol at postnatal days 19-21. We found that propofol exposure significantly increased neuronal apoptosis in the mouse hippocampal dentate gyrus, as evidenced by cleaved caspase-3 immunofluorescence. Additionally, propofol exposure increased the activation and expression of Ras-related C3 botulinum toxin substrate 1 (Rac1) in the dentate gyrus, as shown by western blotting. Modulating Rac1, either through inhibition or overexpression, was found to mitigate or exacerbate propofol-induced neuronal apoptosis, respectively. We further demonstrated that propofol decreased the expression of the anti-apoptotic protein phosphorylated serine/threonine kinase Akt via Rac1. The results of the open field and Morris water maze test further revealed that silencing Rac1 alleviated propofol-induced cognitive dysfunction. Our findings demonstrated that propofol exposure induced neuronal apoptosis and long-term cognitive dysfunction in the mouse hippocampal dentate gyrus by regulating Rac1.
期刊介绍:
Neurochemical Research is devoted to the rapid publication of studies that use neurochemical methodology in research on nervous system structure and function. The journal publishes original reports of experimental and clinical research results, perceptive reviews of significant problem areas in the neurosciences, brief comments of a methodological or interpretive nature, and research summaries conducted by leading scientists whose works are not readily available in English.