Ju Yaojun, Tam Kin Yip
Faculty of Health Sciences, University of Macau, Avenida de Universidade, Taipa, Macau Special Adiministrative Region, China.
Neural Regen Res. 2022 Mar;17(3):543-549. doi: 10.4103/1673-5374.320970.
Alzheimer's disease is a rather complex neurodegenerative disease, which is attributed to a combination of multiple factors. Among the many pathological pathways, synaptic dysfunctions, such as synapses loss and deficits in synaptic plasticity, were thought to be strongly associated with cognitive decline. The deficiencies in various sorts of neurotransmissions are responsible for the multifarious neurodegenerative symptoms in Alzheimer's disease, for example, the cholinergic and glutamatergic deficits for cognitive decline, the excitatory and inhibitory neurotransmission dyshomeostasis for synaptic plasticity deficits and epileptiform symptoms, and the monoamine neurotransmission for neuropsychiatric symptoms. Amyloid cascade hypothesis is the most popular pathological theory to explain Alzheimer's disease pathogenesis and attracts considerable attention. Multiple lines of genetic and pathological evidence support the predominant role of amyloid beta in Alzheimer's disease pathology. Neurofibrillary tangles assembled by microtubule-associated protein tau are other important histopathological characteristics in Alzheimer's disease brains. Cascade of tau toxicity was proved to lead to neuron damage, neuroinflammation and oxidative stress in brain. Ageing is the main risk factor of neurodegenerative diseases, and is associated with inflammation, oxidative stress, reduced metabolism, endocrine insufficiencies and organ failures. These aging related risk factors were also proved to be some of the risk factors contributing to Alzheimer's disease. In Alzheimer's disease drug development, many good therapeutic strategies have been investigated in clinical evaluations. However, complex mechanism of Alzheimer's disease and the interplay among different pathological factors call for the come out of all-powerful therapies with multiple curing functions. This review seeks to summarize some of the representative treatments targeting different pathological pathways currently under clinical evaluations. Multi-target therapies as an emerging strategy for Alzheimer's disease treatment will be highlighted.
阿尔茨海默病是一种相当复杂的神经退行性疾病,它由多种因素共同作用所致。在众多病理途径中,突触功能障碍,如突触丧失和突触可塑性缺陷,被认为与认知衰退密切相关。各种神经传递的缺陷导致了阿尔茨海默病中多种多样的神经退行性症状,例如,胆碱能和谷氨酸能缺陷导致认知衰退,兴奋性和抑制性神经传递失衡导致突触可塑性缺陷和癫痫样症状,单胺神经传递导致神经精神症状。淀粉样蛋白级联假说 是解释阿尔茨海默病发病机制最流行的病理理论,并引起了广泛关注。多条遗传学和病理学证据支持β淀粉样蛋白在阿尔茨海默病病理中的主导作用。由微管相关蛋白tau组装而成的神经原纤维缠结是阿尔茨海默病大脑中其他重要的组织病理学特征。已证明tau毒性级联会导致大脑中的神经元损伤、神经炎症和氧化应激。衰老 是神经退行性疾病的主要危险因素,与炎症、氧化应激、代谢降低、内分泌不足和器官功能衰竭有关。这些与衰老相关的危险因素也被证明是导致阿尔茨海默病的一些危险因素。在阿尔茨海默病药物研发中,许多良好的治疗策略已在临床评估中进行了研究。然而,阿尔茨海默病的复杂机制以及不同病理因素之间的相互作用需要出现具有多种治疗功能的万能疗法。本综述旨在总结目前正在临床评估中的一些针对不同病理途径的代表性治疗方法。多靶点疗法作为一种新兴的阿尔茨海默病治疗策略将被重点介绍。