Department of Zoology, Aligarh Muslim University, Aligarh, U.P., India.
Department of Chemistry, Aligarh Muslim University, Aligarh, U.P., India.
Curr Neuropharmacol. 2023;21(4):867-889. doi: 10.2174/1570159X21666230216104621.
Huntington's disease (HD) is a rare and fatal neurodegenerative disorder with no diseasemodifying therapeutics. HD is characterized by extensive neuronal loss and is caused by the inherited expansion of the huntingtin (HTT) gene that encodes a toxic mutant HTT (mHTT) protein having expanded polyglutamine (polyQ) residues. Current HD therapeutics only offer symptomatic relief. In fact, Food and Drug Administration (FDA) approved two synthetic small-molecule VMAT2 inhibitors, tetrabenazine (1) and deutetrabenazine (2), for managing HD chorea and various other diseases in clinical trials. Therefore, the landscape of drug discovery programs for HD is evolving to discover disease- modifying HD therapeutics. Likewise, numerous natural products are being evaluated at different stages of clinical development and have shown the potential to ameliorate HD pathology. The inherent anti-inflammatory and antioxidant properties of natural products mitigate the mHTT-induced oxidative stress and neuroinflammation, improve mitochondrial functions, and augment the anti-apoptotic and pro-autophagic mechanisms for increased survival of neurons in HD. In this review, we have discussed HD pathogenesis and summarized the anti-HD clinical and pre-clinical natural products, focusing on their therapeutic effects and neuroprotective mechanism/s.
亨廷顿病(HD)是一种罕见的致命神经退行性疾病,目前尚无治疗该病的药物。HD 的特征是广泛的神经元丧失,由亨廷顿(HTT)基因突变引起,该突变导致编码毒性突变 HTT(mHTT)蛋白的 HTT 基因扩展,其具有扩展的多聚谷氨酰胺(polyQ)残基。目前的 HD 治疗方法仅提供对症缓解。事实上,美国食品和药物管理局(FDA)已批准两种合成小分子 VMAT2 抑制剂,即四苯嗪(1)和右苯丙嗪(2),用于临床试验中治疗 HD 舞蹈病和各种其他疾病。因此,用于发现治疗 HD 的疾病修饰疗法的药物发现计划的格局正在发生变化。同样,许多天然产物正在不同的临床开发阶段进行评估,并显示出改善 HD 病理学的潜力。天然产物的固有抗炎和抗氧化特性减轻了 mHTT 诱导的氧化应激和神经炎症,改善了线粒体功能,并增强了抗细胞凋亡和自噬机制,从而增加了 HD 中神经元的存活率。在这篇综述中,我们讨论了 HD 的发病机制,并总结了具有抗 HD 作用的临床和临床前天然产物,重点介绍了它们的治疗效果和神经保护机制。