Department of Neuroscience, San Raffaele Institute and Vita-Salute San Raffaele University, via Olgettina 58, 20132, Milan, Italy.
Pharmacol Res. 2019 Aug;146:104316. doi: 10.1016/j.phrs.2019.104316. Epub 2019 Jun 28.
Alzheimer's is the neurodegenerative disease affecting the largest number of patients in the world. In spite of the intense research of the last decades, progress about its knowledge and therapy was limited. In particular, various cytotoxic processes remained debated, while the few drugs approved for therapy were of only marginal relevance. Recent studies have identified key aspects of the disease, such as the mechanisms governing the development of pathology. In order to operate the Aβ peptide, known as the key factor, requires a complex assembled by its high affinity binding to PrP, a cell surface prion protein, and mGluR5, a metabotropic glutamate receptor. Aβ and its associates bind also phosphorylated tau transferred to the extracellular space, with final activation of intracellular cytotoxic signals. Pathology is further affected by factors (including genes, receptors and their agonists) and by glial cells governing (via vesicles, cytokines and enzymes) cell immunology, inflammation and oxidative stress. Concomitant to pathology studies, strong attempts have been made for the development of new, effective therapies. Critical for this are biomarkers, by which Alzheimer's patients are recognized even before appearance of their symptoms. The question was whether patients take advantage from drugs not yet approved. The latter, first identified in mice, were found effective also in men, however only before appearance or at early stage of the disease. In other words, the drugs not yet approved induce effective protection of patients still healthy or in a preliminary stage of the disease. In contrast, developed Alzheimer's disease is practically irreversible.
阿尔茨海默病是世界上影响患者数量最多的神经退行性疾病。尽管过去几十年进行了大量研究,但在其知识和治疗方面的进展有限。特别是,各种细胞毒性过程仍存在争议,而批准用于治疗的少数几种药物仅具有轻微的相关性。最近的研究已经确定了疾病的关键方面,例如控制病理学发展的机制。为了发挥 Aβ 肽的作用,已知其是关键因素,需要一种由其与 PrP(细胞表面朊病毒蛋白)和 mGluR5(代谢型谷氨酸受体)的高亲和力结合组装而成的复杂结构。Aβ 及其相关物还与转移到细胞外空间的磷酸化 tau 结合,最终激活细胞内细胞毒性信号。病理学还受到因素(包括基因、受体及其激动剂)和神经胶质细胞的影响,这些细胞通过囊泡、细胞因子和酶来控制细胞免疫、炎症和氧化应激。在进行病理学研究的同时,也进行了强烈的尝试来开发新的、有效的治疗方法。这方面的关键是生物标志物,通过它可以在阿尔茨海默病患者出现症状之前识别他们。问题是患者是否能从尚未批准的药物中获益。这些药物最初是在老鼠身上发现的,后来也被发现在男性中有效,但是只有在疾病出现之前或早期才有效。换句话说,尚未批准的药物可以有效地保护仍然健康或处于疾病早期阶段的患者。相比之下,已经发展的阿尔茨海默病几乎是不可逆的。