Department of Pharmacological and Biomolecular Sciences, University of Milan, Via Balzaretti 9, 20133, Milan, Italy.
CNS Drugs. 2020 Mar;34(3):281-297. doi: 10.1007/s40263-020-00705-9.
Alzheimer's disease is a chronic neurodegenerative devastating disorder affecting a high percentage of the population over 65 years of age and causing a relevant emotional, social, and economic burden. Clinically, it is characterized by a prominent cognitive deficit associated with language and behavioral impairments. The molecular pathogenesis of Alzheimer's disease is multifaceted and involves changes in neurotransmitter levels together with alterations of inflammatory, oxidative, hormonal, and synaptic pathways, which may represent a drug target for both prevention and treatment; however, an effective treatment for Alzheimer's disease still represents an unmet goal. As neurotrophic factors participate in the modulation of the above-mentioned pathways, they have been highlighted as critical contributors of Alzheimer's disease etiology, whose modulation might be beneficial for Alzheimer's disease. We focused on the neurotrophin brain-derived neurotrophic factor, providing several lines of evidence pointing to brain-derived neurotrophic factor as a plausible endophenotype of cognitive deficits in Alzheimer's disease, illustrating some of the most recent possibilities to modulate the expression of this neurotrophin in the brain in an attempt to ameliorate cognition and delay the progression of Alzheimer's disease. This review shows that otherwise disparate pharmacologic or non-pharmacologic approaches converge on brain-derived neurotrophic factor, providing a means whereby apparently unrelated medical approaches may nevertheless produce similar synaptic and cognitive outcomes in Alzheimer's disease pathogenesis, suggesting that brain-derived neurotrophic factor-based synaptic repair may represent a modifying strategy to ameliorate cognition in Alzheimer's disease.
阿尔茨海默病是一种慢性神经退行性疾病,影响 65 岁以上人群的高比例,并造成相关的情感、社会和经济负担。临床上,它的特征是明显的认知缺陷,与语言和行为障碍有关。阿尔茨海默病的分子发病机制是多方面的,涉及神经递质水平的变化,以及炎症、氧化、激素和突触途径的改变,这些可能是预防和治疗的药物靶点;然而,阿尔茨海默病的有效治疗仍然是一个未满足的目标。由于神经营养因子参与上述途径的调节,它们被突出为阿尔茨海默病病因的关键贡献者,其调节可能对阿尔茨海默病有益。我们专注于神经营养因子脑源性神经营养因子,提供了一些证据表明脑源性神经营养因子是阿尔茨海默病认知缺陷的一个合理的内表型,说明了一些最近的可能性来调节这种神经营养因子在大脑中的表达,以试图改善认知并延缓阿尔茨海默病的进展。这篇综述表明,否则不同的药物或非药物方法都集中在脑源性神经营养因子上,提供了一种方法,使看似不相关的医学方法在阿尔茨海默病发病机制中仍然可以产生类似的突触和认知结果,这表明基于脑源性神经营养因子的突触修复可能是改善阿尔茨海默病认知的一种修饰策略。