Vigil Neuroscience, Cambridge, MA, USA.
Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Nat Rev Drug Discov. 2024 Jan;23(1):23-42. doi: 10.1038/s41573-023-00823-1. Epub 2023 Nov 27.
Synapse dysfunction and loss are hallmarks of neurodegenerative diseases that correlate with cognitive decline. However, the mechanisms and therapeutic strategies to prevent or reverse synaptic damage remain elusive. In this Review, we discuss recent advances in understanding the molecular and cellular pathways that impair synapses in neurodegenerative diseases, including the effects of protein aggregation and neuroinflammation. We also highlight emerging therapeutic approaches that aim to restore synaptic function and integrity, such as enhancing synaptic plasticity, preventing synaptotoxicity, modulating neuronal network activity and targeting immune signalling. We discuss the preclinical and clinical evidence for each strategy, as well as the challenges and opportunities for developing effective synapse-targeting therapeutics for neurodegenerative diseases.
突触功能障碍和丧失是与认知能力下降相关的神经退行性疾病的特征。然而,预防或逆转突触损伤的机制和治疗策略仍然难以捉摸。在这篇综述中,我们讨论了理解导致神经退行性疾病中突触损伤的分子和细胞途径的最新进展,包括蛋白质聚集和神经炎症的影响。我们还强调了新兴的治疗方法,旨在恢复突触功能和完整性,例如增强突触可塑性、预防突触毒性、调节神经元网络活动和靶向免疫信号。我们讨论了每种策略的临床前和临床证据,以及为神经退行性疾病开发有效的突触靶向治疗方法所面临的挑战和机遇。