Department of Medicine and Biomedical Research Institute, NYU Long Island School of Medicine, Mineola, NY 11501, USA.
Fresno Institute of Neuroscience, Fresno, CA 93730, USA.
Medicina (Kaunas). 2023 Jun 4;59(6):1084. doi: 10.3390/medicina59061084.
As the search for modalities to cure Alzheimer's disease (AD) has made slow progress, research has now turned to innovative pathways involving neural and peripheral inflammation and neuro-regeneration. Widely used AD treatments provide only symptomatic relief without changing the disease course. The recently FDA-approved anti-amyloid drugs, aducanumab and lecanemab, have demonstrated unclear real-world efficacy with a substantial side effect profile. Interest is growing in targeting the early stages of AD before irreversible pathologic changes so that cognitive function and neuronal viability can be preserved. Neuroinflammation is a fundamental feature of AD that involves complex relationships among cerebral immune cells and pro-inflammatory cytokines, which could be altered pharmacologically by AD therapy. Here, we provide an overview of the manipulations attempted in pre-clinical experiments. These include inhibition of microglial receptors, attenuation of inflammation and enhancement of toxin-clearing autophagy. In addition, modulation of the microbiome-brain-gut axis, dietary changes, and increased mental and physical exercise are under evaluation as ways to optimize brain health. As the scientific and medical communities work together, new solutions may be on the horizon to slow or halt AD progression.
由于寻找治疗阿尔茨海默病(AD)的方法进展缓慢,研究现在已经转向涉及神经和外周炎症和神经再生的创新途径。广泛使用的 AD 治疗方法仅提供症状缓解,而不会改变疾病进程。最近 FDA 批准的抗淀粉样蛋白药物 aducanumab 和 lecanemab 具有不明确的实际疗效,且具有大量的副作用。人们越来越感兴趣的是在不可逆的病理变化之前针对 AD 的早期阶段,以便可以保留认知功能和神经元活力。神经炎症是 AD 的一个基本特征,涉及大脑免疫细胞和促炎细胞因子之间的复杂关系,AD 治疗可以通过药理学改变这些关系。在这里,我们提供了在临床前实验中尝试的操作概述。这些包括抑制小胶质细胞受体、减轻炎症和增强清除毒素的自噬。此外,正在评估调节微生物组-大脑-肠道轴、饮食变化以及增加精神和身体锻炼作为优化大脑健康的方法。随着科学界和医学界的合作,可能会有新的解决方案来减缓或阻止 AD 的进展。