Pérez-Arancibia Rodrigo, Cisternas-Olmedo Marisol, Sepúlveda Denisse, Troncoso-Escudero Paulina, Vidal Rene L
Center for Integrative Biology, Faculty of Sciences, Universidad Mayor, Santiago, Chile.
Departamento de Ciencias Básicas, Faculty of Medicine and Science, Universidad San Sebastián, Santiago, Chile.
Front Neurosci. 2023 Jan 9;16:1084493. doi: 10.3389/fnins.2022.1084493. eCollection 2022.
Neurological motor disorders (NMDs) such as Parkinson's disease and Huntington's disease are characterized by the accumulation and aggregation of misfolded proteins that trigger cell death of specific neuronal populations in the central nervous system. Differential neuronal loss initiates the impaired motor control and cognitive function in the affected patients. Although major advances have been carried out to understand the molecular basis of these diseases, to date there are no treatments that can prevent, cure, or significantly delay the progression of the disease. In this context, strategies such as gene editing, cellular therapy, among others, have gained attention as they effectively reduce the load of toxic protein aggregates in different models of neurodegeneration. Nevertheless, these strategies are expensive and difficult to deliver into the patients' nervous system. Thus, small molecules and natural products that reduce protein aggregation levels are highly sought after. Numerous drug discovery efforts have analyzed large libraries of synthetic compounds for the treatment of different NMDs, with a few candidates reaching clinical trials. Moreover, the recognition of new druggable targets for NMDs has allowed the discovery of new small molecules that have demonstrated their efficacy in pre-clinical studies. It is also important to recognize the contribution of natural products to the discovery of new candidates that can prevent or cure NMDs. Additionally, the repurposing of drugs for the treatment of NMDs has gained huge attention as they have already been through clinical trials confirming their safety in humans, which can accelerate the development of new treatment. In this review, we will focus on the new advances in the discovery of small molecules for the treatment of Parkinson's and Huntington's disease. We will begin by discussing the available pharmacological treatments to modulate the progression of neurodegeneration and to alleviate the motor symptoms in these diseases. Then, we will analyze those small molecules that have reached or are currently under clinical trials, including natural products and repurposed drugs.
帕金森病和亨廷顿病等神经运动障碍(NMDs)的特征是错误折叠蛋白的积累和聚集,这些蛋白会引发中枢神经系统中特定神经元群体的细胞死亡。不同神经元的丧失导致受影响患者的运动控制和认知功能受损。尽管在理解这些疾病的分子基础方面已经取得了重大进展,但迄今为止,尚无能够预防、治愈或显著延缓疾病进展的治疗方法。在这种背景下,基因编辑、细胞疗法等策略受到了关注,因为它们能有效降低不同神经退行性疾病模型中有毒蛋白聚集体的负荷。然而,这些策略成本高昂且难以递送至患者的神经系统。因此,能降低蛋白聚集水平的小分子和天然产物备受追捧。众多药物研发工作分析了大量合成化合物库以用于治疗不同的神经运动障碍,只有少数候选药物进入了临床试验。此外,对神经运动障碍新的可成药靶点的认识使得发现了一些在临床前研究中已证明其疗效的新小分子。认识天然产物对发现可预防或治愈神经运动障碍的新候选药物的贡献也很重要。此外,将药物重新用于治疗神经运动障碍也备受关注,因为这些药物已经过临床试验,证实了其在人体中的安全性,这可以加速新治疗方法的开发。在本综述中,我们将重点关注治疗帕金森病和亨廷顿病的小分子发现方面的新进展。我们将首先讨论现有的药理学治疗方法,以调节神经退行性变的进展并缓解这些疾病中的运动症状。然后,我们将分析那些已进入或目前正在进行临床试验的小分子,包括天然产物和重新利用的药物。