Altered synaptic currents, mitophagy, mitochondrial dynamics in Alzheimer's disease models and therapeutic potential of Dengzhan Shengmai capsules intervention

被引:12
作者
Zhao, Binbin [1 ,2 ,3 ]
Wei, Dongfeng [4 ]
Long, Qinghua [5 ]
Chen, Qingjie [6 ]
Wang, Fushun [7 ]
Chen, Linlin [8 ]
Li, Zefei [3 ]
Li, Tong [3 ]
Ma, Tao [9 ]
Liu, Wei [10 ]
Wang, Linshuang [4 ]
Yang, Caishui [1 ,2 ,11 ]
Zhang, Xiaxia [1 ,2 ,12 ]
Wang, Ping [3 ]
Zhang, Zhanjun [1 ,2 ,12 ]
机构
[1] Beijing Normal Univ, State Key Lab Cognit Neurosci & Learning, Beijing 100875, Peoples R China
[2] Beijing Normal Univ, IDG McGovern Inst Brain Res, Beijing 100875, Peoples R China
[3] Hubei Univ Chinese Med, Inst Gerontol, Wuhan 430065, Peoples R China
[4] China Acad Chinese Med Sci, Inst Basic Res Clin Med, Beijing 100700, Peoples R China
[5] Hubei Minzu Univ, Med Sch, Enshi 445000, Hubei, Peoples R China
[6] Hubei Univ Sci & Technol, Xianning 437100, Hubei, Peoples R China
[7] Sichuan Normal Univ, Inst Brain & Psychol Sci, Chengdu 610066, Peoples R China
[8] Hubei Univ Chinese Med, Key Lab Tradit Chinese Med Resource & Cpd Prescrip, Minist Educ, Wuhan 430065, Peoples R China
[9] Beijing Univ Chinese Med, Dongfang Hosp, Beijing 100078, Peoples R China
[10] China Acad Chinese Med Sci, Expt Res Ctr, Beijing Key Lab Tradit Chinese Med Basic Res Preve, Beijing 100700, Peoples R China
[11] Beijing Normal Univ, Sch Syst Sci, Beijing 100875, Peoples R China
[12] Beijing Normal Univ, BABRI Ctr, Beijing 100875, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; Synaptic currents; Mitophagy; Mitochondrial fusion and fission; Dengzhan Shengmai capsules; PATHOPHYSIOLOGY; DYSFUNCTION; MECHANISMS; NETWORK; IMPAIRS; MEMORY;
D O I
10.1016/j.jpha.2023.10.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Emerging research suggests a potential association of progression of Alzheimer's disease (AD) with alterations in synaptic currents and mitochondrial dynamics. However, the specific associations between these pathological changes remain unclear. In this study, we utilized Af342-induced AD rats and primary neural cells as in vivo and in vitro models. The investigations included behavioural tests, brain magnetic resonance imaging (MRI), liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) analysis, Nissl staining, thioflavin-S staining, enzyme-linked immunosorbent assay, Golgi-Cox staining, transmission electron microscopy (TEM), immunofluorescence staining, proteomics, adenosine triphosphate (ATP) detection, mitochondrial membrane potential (MMP) and reactive oxygen species (ROS) assessment, mitochondrial morphology analysis, electrophysiological studies, Western blotting, and molecular docking. The results revealed changes in synaptic currents, mitophagy, and mitochondrial dynamics in the AD models. Remarkably, intervention with Dengzhan Shengmai (DZSM) capsules emerged as a pivotal element in this investigation. Af342-induced synaptic dysfunction was significantly mitigated by DZSM intervention, which notably amplified the frequency and amplitude of synaptic transmission. The cognitive impairment observed in AD rats was ameliorated and accompanied by robust protection against structural damage in key brain regions, including the hippocampal CA3, primary cingular cortex, prelimbic system, and dysgranular insular cortex. DZSM intervention led to increased IDE levels, augmented long-term potential (LTP) amplitude, and enhanced dendritic spine density and length. Moreover, DZSM intervention led to favourable changes in mitochondrial parameters, including ROS expression, MMP and ATP contents, and mitochondrial morphology. In conclusion, our findings delved into the realm of altered synaptic currents, mitophagy, and mitochondrial dynamics in AD, concurrently highlighting the therapeutic potential of DZSM intervention. (c) 2023 The Authors. Published by Elsevier B.V. on behalf of Xi 'an Jiaotong University. This is an open access article under the CC BY -NC -ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:348 / 370
页数:23
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