School of Life Sciences, Kyungpook National University, Daegu 41566, Korea.
BK21 FOUR KNU Creative BioResearch Group, Kyungpook National University, Daegu 41566, Korea.
Int J Mol Sci. 2021 May 3;22(9):4850. doi: 10.3390/ijms22094850.
Alzheimer's disease (AD) is the most frequent cause of age-related neurodegeneration and cognitive impairment, and there are currently no broadly effective therapies. The underlying pathogenesis is complex, but a growing body of evidence implicates mitochondrial dysfunction as a common pathomechanism involved in many of the hallmark features of the AD brain, such as formation of amyloid-beta (Aβ) aggregates (amyloid plaques), neurofibrillary tangles, cholinergic system dysfunction, impaired synaptic transmission and plasticity, oxidative stress, and neuroinflammation, that lead to neurodegeneration and cognitive dysfunction. Indeed, mitochondrial dysfunction concomitant with progressive accumulation of mitochondrial Aβ is an early event in AD pathogenesis. Healthy mitochondria are critical for providing sufficient energy to maintain endogenous neuroprotective and reparative mechanisms, while disturbances in mitochondrial function, motility, fission, and fusion lead to neuronal malfunction and degeneration associated with excess free radical production and reduced intracellular calcium buffering. In addition, mitochondrial dysfunction can contribute to amyloid-β precursor protein (APP) expression and misprocessing to produce pathogenic fragments (e.g., Aβ1-40). Given this background, we present an overview of the importance of mitochondria for maintenance of neuronal function and how mitochondrial dysfunction acts as a driver of cognitive impairment in AD. Additionally, we provide a brief summary of possible treatments targeting mitochondrial dysfunction as therapeutic approaches for AD.
阿尔茨海默病(AD)是最常见的与年龄相关的神经退行性疾病和认知障碍的原因,目前尚无广泛有效的治疗方法。其潜在的发病机制很复杂,但越来越多的证据表明线粒体功能障碍是 AD 大脑许多标志性特征的共同病理机制,例如淀粉样β(Aβ)聚集体(淀粉样斑块)、神经原纤维缠结、胆碱能系统功能障碍、突触传递和可塑性受损、氧化应激和神经炎症的形成,这些都会导致神经退行性变和认知功能障碍。事实上,线粒体功能障碍伴随着线粒体 Aβ 的进行性积累,是 AD 发病机制中的早期事件。健康的线粒体对于提供足够的能量来维持内源性神经保护和修复机制至关重要,而线粒体功能、运动、分裂和融合的紊乱会导致神经元功能障碍和退化,导致过量的自由基产生和细胞内钙缓冲减少。此外,线粒体功能障碍可导致淀粉样前体蛋白(APP)表达和错误处理,产生致病片段(如 Aβ1-40)。有鉴于此,我们概述了线粒体对维持神经元功能的重要性,以及线粒体功能障碍如何作为 AD 认知障碍的驱动因素。此外,我们简要总结了靶向线粒体功能障碍的可能治疗方法作为 AD 的治疗方法。