Zheng Chao, Xia Weiming, Zhang Jianhua
Azrieli Centre for Neuro-Radiochemistry, Brain Health Imaging Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada.
Departments of Psychiatry, Chemistry, Pharmacology and Toxicology, University of Toronto, Toronto, ON, Canada.
Front Aging. 2025 Mar 20;6:1547883. doi: 10.3389/fragi.2025.1547883. eCollection 2025.
Alzheimer's disease (AD) is the most common age-related neurodegenerative disease and cause of dementia. AD pathology primarily involves the formation of amyloid β (Aβ) plaques and neurofibrillary tangles containing hyperphosphorylated tau (p-tau). While Aβ targeted treatments have shown clinical promise, other aspects of AD pathology such as microgliosis, astrocytosis, synaptic loss, and hypometabolism may be viable targets for treatment. Among notable novel therapeutic approaches, the Ras homolog (Rho)-associated kinases (ROCKs) are being investigated as targets for AD treatment, based on the observations that ROCK1/2 levels are elevated in AD, and activation or inhibition of ROCKs changes dendritic/synaptic structures, protein aggregate accumulation, inflammation, and gliosis. This review will highlight key findings on the effects of ROCK inhibition in Aβ and ptau pathologies, as well as its effects on neuroinflammation, synaptic density, and potentially metabolism and bioenergetics.
阿尔茨海默病(AD)是最常见的与年龄相关的神经退行性疾病及痴呆病因。AD病理主要涉及淀粉样β(Aβ)斑块的形成以及含有高度磷酸化tau(p-tau)的神经原纤维缠结。虽然针对Aβ的治疗已展现出临床前景,但AD病理的其他方面,如小胶质细胞增生、星形细胞增生、突触丧失和代谢减退,可能也是可行的治疗靶点。在值得关注的新型治疗方法中,基于Ras同源物(Rho)相关激酶(ROCKs)在AD中水平升高,以及ROCKs的激活或抑制会改变树突/突触结构、蛋白质聚集体积累、炎症和胶质细胞增生的观察结果,ROCKs正作为AD治疗的靶点进行研究。本综述将重点介绍ROCK抑制在Aβ和p-tau病理方面的关键发现,以及其对神经炎症、突触密度以及潜在的代谢和生物能量学的影响。