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低频重复经颅磁刺激改善阿尔茨海默病APP23/PS45小鼠模型的认知功能和突触可塑性

Low-Frequency Repetitive Transcranial Magnetic Stimulation Ameliorates Cognitive Function and Synaptic Plasticity in APP23/PS45 Mouse Model of Alzheimer's Disease.

作者信息

Huang Zhilin, Tan Tao, Du Yehong, Chen Long, Fu Min, Yu Yanzhi, Zhang Lu, Song Weihong, Dong Zhifang

机构信息

Ministry of Education Key Laboratory of Child Development and Disorders, Children's Hospital of Chongqing Medical UniversityChongqing, China.

Chongqing Key Laboratory of Translational Medical Research in Cognitive Development and Learning and Memory Disorders, Children's Hospital of Chongqing Medical UniversityChongqing, China.

出版信息

Front Aging Neurosci. 2017 Sep 12;9:292. doi: 10.3389/fnagi.2017.00292. eCollection 2017.

Abstract

Alzheimer's disease (AD) is a chronic neurodegenerative disease leading to dementia, which is characterized by progressive memory loss and other cognitive dysfunctions. Recent studies have attested that noninvasive repetitive transcranial magnetic stimulation (rTMS) may help improve cognitive function in patients with AD. However, the majority of these studies have focused on the effects of high-frequency rTMS on cognitive function, and little is known about low-frequency rTMS in AD treatment. Furthermore, the potential mechanisms of rTMS on the improvement of learning and memory also remain poorly understood. In the present study, we reported that severe deficits in spatial learning and memory were observed in APP23/PS45 double transgenic mice, a well known mouse model of AD. Furthermore, these behavioral changes were accompanied by the impairment of long-term potentiation (LTP) in the CA1 region of hippocampus, a brain region vital to spatial learning and memory. More importantly, 2-week low-frequency rTMS treatment markedly reversed the impairment of spatial learning and memory as well as hippocampal CA1 LTP. In addition, low-frequency rTMS dramatically reduced amyloid-β precursor protein (APP) and its C-terminal fragments (CTFs) including C99 and C89, as well as β-site APP-cleaving enzyme 1 (BACE1) in the hippocampus. These results indicate that low-frequency rTMS noninvasively and effectively ameliorates cognitive and synaptic functions in a mouse model of AD, and the potential mechanisms may be attributed to rTMS-induced reduction in Aβ neuropathology.

摘要

阿尔茨海默病(AD)是一种导致痴呆的慢性神经退行性疾病,其特征为进行性记忆丧失和其他认知功能障碍。最近的研究证实,无创重复经颅磁刺激(rTMS)可能有助于改善AD患者的认知功能。然而,这些研究大多集中在高频rTMS对认知功能的影响上,而关于低频rTMS在AD治疗中的作用知之甚少。此外,rTMS改善学习和记忆的潜在机制也仍未得到充分理解。在本研究中,我们报告称,在APP23/PS45双转基因小鼠(一种著名的AD小鼠模型)中观察到空间学习和记忆存在严重缺陷。此外,这些行为变化伴随着海马体CA1区长期增强(LTP)的受损,海马体是对空间学习和记忆至关重要的脑区。更重要的是,为期2周的低频rTMS治疗显著逆转了空间学习和记忆以及海马体CA1区LTP的损伤。此外,低频rTMS显著降低了海马体中淀粉样前体蛋白(APP)及其C端片段(CTF),包括C99和C89,以及β-位点APP裂解酶1(BACE1)。这些结果表明,低频rTMS可无创且有效地改善AD小鼠模型的认知和突触功能,其潜在机制可能归因于rTMS诱导的Aβ神经病理学的减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5055/5600921/ea1ce57f1514/fnagi-09-00292-g0001.jpg

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