Laboratory of Neurosciences - LIM27, Departamento e Instituto de Psiquiatria, Hospital das Clínicas HCFMUSP, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Laboratory of Neurosciences - LIM27, Departamento e Instituto de Psiquiatria, Hospital das Clínicas HCFMUSP, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Neurosci Lett. 2021 Aug 24;760:136078. doi: 10.1016/j.neulet.2021.136078. Epub 2021 Jun 20.
Alzheimer's disease (AD) is one of the most prevalent neurodegenerative diseases, characterized by the accumulation of abnormal tau proteins within neurons and amyloid plaques in the brain parenchyma, which leads to progressive loss of neurons in the brain. While the detailed mechanism of the pathogenesis of AD is still unknown, evidence suggests that mitochondrial dysfunction likely plays a fundamental role in the pathogenesis of this disease. Due to the relevance of mitochondrial alterations in AD, recent works have suggested the therapeutic potential of mitochondrial-targeted lithium. Lithium has been shown to possess neuroprotective and neurotrophic properties that could also be related to the upregulation of mitochondrial function. In the current work, we perform a comprehensive investigation of the significance of mitochondrial dysfunction in AD and pharmacological treatment with lithium as imperative in this pathology, through a brief review of the major findings on the effects of lithium as a therapeutic approach targeting mitochondria in the context of AD.
阿尔茨海默病(AD)是最常见的神经退行性疾病之一,其特征是神经元内异常的 tau 蛋白和脑实质中的淀粉样斑块积累,导致大脑神经元进行性丧失。虽然 AD 发病机制的详细机制尚不清楚,但有证据表明线粒体功能障碍可能在该疾病的发病机制中起基础性作用。由于线粒体改变与 AD 的相关性,最近的研究表明线粒体靶向锂具有治疗潜力。锂已被证明具有神经保护和神经营养特性,这也可能与线粒体功能的上调有关。在目前的工作中,我们通过简要回顾锂作为治疗方法在 AD 背景下靶向线粒体的主要发现,全面研究了线粒体功能障碍在 AD 中的意义以及锂的药理学治疗的必要性。