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Long-term exposure to ELF-MF ameliorates cognitive deficits and attenuates tau hyperphosphorylation in 3xTg AD mice

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单位: [1]Huazhong Univ Sci & Technol, Dept Pathophysiol, Minist Educ Neurol Disorders, Sch Basal Med,Tongji Med Coll,Key Lab, Wuhan 430030, Peoples R China [2]Nantong Univ, Coinnovat Ctr Neuroregenerat, Nantong 226001, Peoples R China [3]Huazhong Univ Sci & Technol, Tongji Hosp, Div Cardiol, Dept Internal Med,Tongji Med Coll, 1095 Jiefang Ave, Wuhan 430030, Peoples R China [4]China Elect Power Res Inst, High Voltage Res Inst, State Key Lab Power Grid Environm Protect, Wuhan 430074, Peoples R China
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关键词: Alzheimer's disease ELF-MF Tau phosphorylation Cognitive

摘要:
Although numerous studies have reported the influence of extremely low frequency magnetic field (ELF-MF) exposure on human health, its effects on cognitive deficits in Alzheimer's disease (AD) have remained under debate. Moreover, the influence of ELF-MF on hyperphosphorylated tau, which is one of the most common pathological hallmarks of AD, has not been reported to date. Therefore, transgenic mice (3xTg) were used in the present study. 3xTg mice, which express an APP/PSI mutation combined with a tau (P301L) mutation and that develop cognitive deficits at 6 months of age, were subjected to ELF-MF (50 Hz, 500 mu T) exposure or sham exposure daily for 3 months. We discovered that ELF-MF exposure ameliorated cognitive deficits and increased synaptic proteins in 3xTg mice. The protective effects of ELF-MF exposure may have also been caused by the inhibition of apoptosis and/or decreased oxidative stress levels that were observed in the hippocampus tissues of treated mice. Furthermore, tau hyperphosphorylation was decreased in vivo because of ELF-MF exposure, and this decrease was induced by the inhibition of GSK3 beta and CDK5 activities and activation of PP2Ac. We are the first to report that exposure to ELF-MF can attenuate tau phosphorylation. These findings suggest that ELF-MF exposure could act as a valid therapeutic strategy for ameliorating cognitive deficits and attenuating tau hyperphosphorylation in AD. (C) 2016 Elsevier Inc. All rights reserved.

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出版当年[2015]版:
大类 | 3 区 医学
小类 | 3 区 药学 3 区 毒理学 4 区 神经科学
最新[2025]版:
大类 | 3 区 医学
小类 | 2 区 毒理学 3 区 神经科学 3 区 药学
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出版当年[2014]版:
Q1 TOXICOLOGY Q2 PHARMACOLOGY & PHARMACY Q2 NEUROSCIENCES
最新[2023]版:
Q2 NEUROSCIENCES Q2 PHARMACOLOGY & PHARMACY Q2 TOXICOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2014版] 出版当年五年平均 出版前一年[2013版] 出版后一年[2015版]

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第一作者单位: [1]Huazhong Univ Sci & Technol, Dept Pathophysiol, Minist Educ Neurol Disorders, Sch Basal Med,Tongji Med Coll,Key Lab, Wuhan 430030, Peoples R China
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通讯机构: [1]Huazhong Univ Sci & Technol, Dept Pathophysiol, Minist Educ Neurol Disorders, Sch Basal Med,Tongji Med Coll,Key Lab, Wuhan 430030, Peoples R China [2]Nantong Univ, Coinnovat Ctr Neuroregenerat, Nantong 226001, Peoples R China
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