Rademacher David J, Exline Jacob E, Foecking Eileen M
Department of Microbiology and Immunology and Core Microscopy Facility, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USA.
Neuroscience Graduate Program, Loyola University Chicago, Maywood, IL 60153, USA.
Biomedicines. 2025 Jun 7;13(6):1400. doi: 10.3390/biomedicines13061400.
Parkinson's disease (PD) is an aging-related neurodegenerative disease characterized by a progressive loss of dopamine (DA)-secreting neurons in the substantia nigra. Most of the currently available treatments attempt to alleviate the disease symptoms by increasing DA transmission in the brain and are associated with unpleasant side effects. Since there are no treatments that modify the course of PD or regenerate DA neurons, identifying therapeutic strategies that slow, stop, or reverse cell death in PD is of critical importance. Here, factors that confer vulnerability of substantia nigra DA neurons to cell death and the primary mechanisms of PD pathogenesis, including cellular senescence, a cellular stress response that elicits a stable cell cycle arrest in mitotic cells and profound phenotypic changes including the implementation of a pro-inflammatory secretome, are reviewed. Additionally, a discussion of the characteristics, mechanisms, and markers of cellular senescence and the development of approaches to target senescent cells, referred to as senotherapeutics, is included. Although the senotherapeutics curcumin, fisetin, GSK-650394, and astragaloside IV had disease-modifying effects in in vitro and in vivo models of PD, the potential long-term side effects of these compounds remain unclear. It remains to be elucidated whether their beneficial effects will translate to non-human primate models and/or human PD patients. The enhanced selectivity, safety, and/or efficacy of next generation senotherapeutic strategies including senolytic peptides, senoreverters, proteolysis-targeting chimeras, pro-drugs, immunotherapy, and nanoparticles will also be reviewed. Although these next generation senotherapeutics may have advantages, none have been tried in models of PD.
帕金森病(PD)是一种与衰老相关的神经退行性疾病,其特征是黑质中分泌多巴胺(DA)的神经元逐渐丧失。目前大多数可用的治疗方法试图通过增加大脑中的DA传递来缓解疾病症状,但都伴有令人不适的副作用。由于尚无能够改变PD病程或使DA神经元再生的治疗方法,因此确定能够延缓、阻止或逆转PD中细胞死亡的治疗策略至关重要。本文综述了使黑质DA神经元易发生细胞死亡的因素以及PD发病机制的主要机制,包括细胞衰老,这是一种细胞应激反应,可导致有丝分裂细胞稳定地停滞在细胞周期中,并引发深刻的表型变化,包括促炎分泌组的形成。此外,还讨论了细胞衰老的特征、机制和标志物,以及针对衰老细胞的方法(称为衰老疗法)的发展。尽管衰老疗法姜黄素、非瑟酮、GSK-650394和黄芪甲苷IV在PD的体外和体内模型中具有疾病修饰作用,但这些化合物潜在的长期副作用仍不清楚。它们的有益效果是否能转化到非人类灵长类动物模型和/或人类PD患者身上仍有待阐明。还将综述包括溶酶体肽、逆转衰老剂、蛋白酶靶向嵌合体、前药、免疫疗法和纳米颗粒在内的下一代衰老疗法的更高选择性、安全性和/或有效性。尽管这些下一代衰老疗法可能具有优势,但尚未在PD模型中进行试验。