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Electroacupuncture Alleviates Memory Deficits in APP/PS1 Mice by Targeting Serotonergic Neurons in Dorsal Raphe Nucleus

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收录情况: ◇ SCIE ◇ 卓越:梯队期刊

机构: [1]Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Rehabil, Wuhan 430022, Peoples R China [2]Shenzhen Tradit Chinese Med Hosp, Dept Tuina, Shenzhen 518000, Peoples R China [3]Guangzhou Univ Chinese Med, Clin Coll 4, Shenzhen 518000, Peoples R China [4]Wuhan Univ, Wuhan Hosp 3, Tongren Hosp, Dept Rehabil, Wuhan 430074, Peoples R China [5]Wuhan Hosp Integrated Tradit Chinese & Western Med, Dept Acupuncture & Moxibust, Wuhan 430030, Peoples R China [6]Hubei Univ Chinese Med, Coll Acupuncture & Orthoped, Wuhan 430065, Peoples R China [7]Hebei Univ Chinese Med, Coll Acupuncture Moxibust & Tuina, Shijiazhuang 050299, Peoples R China [8]Qujing Hosp Matern & Childcare, Dept Child Rehabil Med, Qujing 655002, Peoples R China
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关键词: Alzheimer's disease electroacupuncture dorsal raphe nucleus hippocampus serotonergic neurons glutamatergic neurons 5-HT1B cognitive impairment chemogenetic manipulation synaptic plasticity

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ObjectiveAlzheimer's disease (AD) has become a significant global concern, but effective drugs able to slow down AD progression is still lacked. Electroacupuncture (EA) has been demonstrated to ameliorate cognitive impairment in individuals with AD. However, the underlying mechanisms remains poorly understood. This study aimed at examining the neuroprotective properties of EA and its potential mechanism of action against AD.MethodsAPP/PS1 transgenic mice were employed to evaluate the protective effects of EA on Shenshu (BL 23) and Baihui (GV 20). Chemogenetic manipulation was used to activate or inhibit serotonergic neurons within the dorsal raphe nucleus (DRN). Learning and memory abilities were assessed by the novel object recognition and Morris water maze tests. Golgi staining, western blot, and immunostaining were utilized to determine EA-induced neuroprotection.ResultsEA at Shenshu (BL 23) and Baihui (GV 20) effectively ameliorated learning and memory impairments in APP/PS1 mice. EA attenuated dendritic spine loss, increased the expression levels of PSD95, synaptophysin, and brain-derived neurotrophic factor in hippocampus. Activation of serotonergic neurons within the DRN can ameliorate cognitive deficits in AD by activating glutamatergic neurons mediated by 5-HT1B. Chemogenetic inhibition of serotonergic neurons in the DRN reversed the effects of EA on synaptic plasticity and memory.ConclusionEA can alleviate cognitive dysfunction in APP/PS1 mice by activating serotonergic neurons in the DRN. Further study is necessary to better understand how the serotonergic neurons-related neural circuits involves in EA-induced memory improvement in AD.

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出版当年[2023]版:
大类 | 4 区 医学
小类 | 4 区 医学:研究与实验
最新[2025]版:
大类 | 4 区 医学
小类 | 4 区 医学:研究与实验
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出版当年[2022]版:
Q3 MEDICINE, RESEARCH & EXPERIMENTAL
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Q3 MEDICINE, RESEARCH & EXPERIMENTAL

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第一作者机构: [1]Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Rehabil, Wuhan 430022, Peoples R China [2]Shenzhen Tradit Chinese Med Hosp, Dept Tuina, Shenzhen 518000, Peoples R China [3]Guangzhou Univ Chinese Med, Clin Coll 4, Shenzhen 518000, Peoples R China
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