Aging and Alzheimer's: the critical role of mitochondrial dysfunction and synaptic alterations.

IF 6.9 4区 医学 Q2 NEUROSCIENCES
Frontiers in Synaptic Neuroscience Pub Date : 2026-01-02 eCollection Date: 2025-01-01 DOI:10.3389/fnsyn.2025.1676317
Pinky, Zitin Wali, Neha, Prachi Tiwari, Mohamed El-Tanani, Syed Arman Rabbani, Suhel Parvez
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引用次数: 0

Abstract

Alzheimer's disease is a progressive neurodegenerative disorder marked by cognitive decline, accumulation of amyloid-β plaques and neurofibrillary tangles, synaptic dysfunction, and mitochondrial impairment. Despite multiple therapeutic strategies, currently available treatments only provide symptomatic relief without halting disease progression. Emerging evidence implicates mitochondrial dysfunction-including oxidative stress, impaired calcium signaling, mitophagy deficits, disrupted proteostasis, and electron transport chain abnormalities, as central to AD pathogenesis. These dysfunctions contribute to synaptic degeneration, increased reactive oxygen species, and neuronal death. This review consolidates current knowledge on the mechanistic pathways of mitochondrial impairment in AD and their downstream effects on neuronal health. We also explore the therapeutic potential of multitarget approaches, including agents targeting Aβ and tau pathology, oxidative stress mitigation, mitochondrial quality control, and synaptic restoration. By integrating evidence from recent preclinical and clinical studies, this work highlights mitochondrial homeostasis as a promising frontier for disease-modifying therapies in AD.

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衰老和阿尔茨海默病:线粒体功能障碍和突触改变的关键作用。
阿尔茨海默病是一种进行性神经退行性疾病,其特征是认知能力下降、淀粉样蛋白-β斑块和神经原纤维缠结积累、突触功能障碍和线粒体损伤。尽管有多种治疗策略,但目前可用的治疗方法只能提供症状缓解,而不能阻止疾病进展。新出现的证据表明,线粒体功能障碍,包括氧化应激、钙信号受损、线粒体自噬缺陷、蛋白质平衡中断和电子传递链异常,是AD发病的核心。这些功能障碍导致突触变性、活性氧增加和神经元死亡。这篇综述巩固了目前关于阿尔茨海默病线粒体损伤的机制途径及其对神经元健康的下游影响的知识。我们还探索了多靶点方法的治疗潜力,包括靶向Aβ和tau病理,氧化应激缓解,线粒体质量控制和突触恢复的药物。通过整合最近临床前和临床研究的证据,这项工作强调了线粒体稳态是阿尔茨海默病疾病改善治疗的一个有前途的前沿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.10
自引率
2.70%
发文量
74
审稿时长
14 weeks
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