Institute of Cytology of Russian Academy of Sciences, Tikhoretsky Ave. 4, 194064 St. Petersburg, Russia.
Department of Organic and Biomolecular Chemistry, Ural Federal University, Mira Street, 19, 620002 Ekaterinburg, Russia.
Molecules. 2022 Dec 15;27(24):8950. doi: 10.3390/molecules27248950.
The risk of progression of most sporadic neurodegenerative diseases, including Alzheimer's disease, increases with age. Traditionally, this is associated with a decrease in the efficiency of cell protection systems, in particular, molecular chaperones. Thus, the development of small molecules able to induce the synthesis of chaperones is a promising therapeutic approach to prevent neural diseases associated with ageing. Here, we describe a new compound , belonging to the class of indolylazines and featured by a low size of topological polar surface area, the property related to substances with potentially high membrane-penetrating activity. We also estimated the absorption, distribution, metabolism and excretion characteristics of and found the substance to fit the effective drug criteria. The new compound was found to induce the synthesis and accumulation of Hsp70 in normal and aged neurons and in the hippocampi of young and old mice. The transgenic model of Alzheimer's disease, based on 5xFAD mice, confirmed that the injection of prevented the formation of β-amyloid aggregates, loss of hippocampal neurons and the development of memory impairment. These data indicate that this novel substance may induce the expression of chaperones in neural cells and brain tissues, suggesting its possible application in the therapy of ageing-associated disorders.
大多数散发性神经退行性疾病(包括阿尔茨海默病)的进展风险随着年龄的增长而增加。传统上,这与细胞保护系统效率的降低有关,特别是分子伴侣。因此,开发能够诱导伴侣蛋白合成的小分子是预防与衰老相关的神经疾病的一种有前途的治疗方法。在这里,我们描述了一种新的化合物,属于吲唑类,具有低拓扑极性表面积,这一特性与具有潜在高膜穿透活性的物质有关。我们还估计了[化合物名称]的吸收、分布、代谢和排泄特征,发现该物质符合有效药物的标准。该新化合物被发现诱导正常和衰老神经元以及年轻和老年小鼠海马中 Hsp70 的合成和积累。基于 5xFAD 小鼠的阿尔茨海默病转基因模型证实,注射[化合物名称]可防止β-淀粉样蛋白聚集的形成、海马神经元的丧失和记忆障碍的发展。这些数据表明,这种新型物质可能在神经细胞和脑组织中诱导伴侣蛋白的表达,提示其在治疗与衰老相关的疾病方面的潜在应用。