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阿尔茨海默病及相关tau 病的治疗靶点。

Therapeutic targets in Alzheimer's disease and related tauopathies.

机构信息

College of Staten Island, Program in evelopmental Neuroscience, The Graduate Center, City University of New York (CUNY), Staten Island, New York, USA.

出版信息

Prog Mol Biol Transl Sci. 2011;98:47-83. doi: 10.1016/B978-0-12-385506-0.00002-8.

DOI:10.1016/B978-0-12-385506-0.00002-8
PMID:21199770
Abstract

Alzheimer's disease is a progressive neurodegenerative disease that is characterized histopathologically by the presence of plaques, mainly composed of Abeta amyloid and the tangles, mainly composed of hyperphosphorylated tau. To date, there is no treatment that can reverse the disease, and all the current therapeutics is directed to cope with the symptoms of the disease. Here we describe the efforts dedicated to attack the plaques and, in more detail, the process of neurofibrillary degeneration, linked to the presence of the hyperphosphorylated microtubule associated protein tau. We have identified the different putative targets for therapeutics and the current knowledge on them.

摘要

阿尔茨海默病是一种进行性神经退行性疾病,其组织病理学特征是存在斑块,主要由 Abeta 淀粉样蛋白组成,以及缠结,主要由过度磷酸化的 tau 组成。迄今为止,尚无能够逆转该疾病的治疗方法,目前所有的治疗方法都旨在应对该疾病的症状。在这里,我们描述了针对斑块的治疗方法,更详细地描述了与过度磷酸化的微管相关蛋白 tau 存在相关的神经纤维变性过程。我们已经确定了不同的潜在治疗靶点及其目前的知识。

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Therapeutic targets in Alzheimer's disease and related tauopathies.阿尔茨海默病及相关tau 病的治疗靶点。
Prog Mol Biol Transl Sci. 2011;98:47-83. doi: 10.1016/B978-0-12-385506-0.00002-8.
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Alpha1-antichymotrypsin, an inflammatory protein overexpressed in Alzheimer's disease brain, induces tau phosphorylation in neurons.α1-抗糜蛋白酶是一种在阿尔茨海默病大脑中过度表达的炎症蛋白,可诱导神经元中的tau蛋白磷酸化。
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The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics.阿尔茨海默病的淀粉样蛋白假说:治疗之路上的进展与问题
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The amyloid peptide and its precursor in Alzheimer's disease.阿尔茨海默病中的淀粉样肽及其前体。
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[Neurofibrillary tangles and early modification of the neuronal cytoskeleton in Alzheimer's disease and in experimental models].[阿尔茨海默病及实验模型中的神经原纤维缠结与神经元细胞骨架的早期改变]
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引用本文的文献

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Neuraminidase as a novel therapeutic management strategy for Alzheimer's disease: evidenced through molecular docking, molecular dynamic simulation and gene expression analysis.神经氨酸酶作为阿尔茨海默病的一种新型治疗策略:通过分子对接、分子动力学模拟和基因表达分析得到证实。
Front Chem. 2025 May 30;13:1574702. doi: 10.3389/fchem.2025.1574702. eCollection 2025.
2
Preliminary exploration of the co-regulation of Alzheimer's disease pathogenic genes by microRNAs and transcription factors.微小RNA与转录因子对阿尔茨海默病致病基因的共同调控的初步探索
Front Aging Neurosci. 2022 Dec 6;14:1069606. doi: 10.3389/fnagi.2022.1069606. eCollection 2022.
3
Hyperphosphorylation of Tau Associates With Changes in Its Function Beyond Microtubule Stability.
Tau蛋白的过度磷酸化与其在微管稳定性之外的功能变化相关。
Front Cell Neurosci. 2018 Oct 9;12:338. doi: 10.3389/fncel.2018.00338. eCollection 2018.
4
Tau-induced neurodegeneration: mechanisms and targets.tau蛋白诱导的神经退行性变:机制与靶点
Neurosci Bull. 2014 Apr;30(2):346-58. doi: 10.1007/s12264-013-1414-z. Epub 2014 Apr 15.
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Neurogenesis in Alzheimer´s disease: a realistic alternative to neuronal degeneration?阿尔茨海默病中的神经发生:神经元变性的一种可行替代方案?
Curr Signal Transduct Ther. 2011 Sep 1;6(3):314-319. doi: 10.2174/157436211797483949.