Department of Physiology, Capital Medical University, Youanmen, Beijing, PR China.
CNS Neurol Disord Drug Targets. 2010 Apr;9(2):232-40. doi: 10.2174/187152710791012035.
Parkinson's disease (PD) is a type of motor system disorder that results from the progressive loss of dopaminergic (DAergic) neurons in the substantia nigra (SN) of the midbrain. It is one of the most common neurodegenerative disorders, with an incidence that is second only to Alzheimer's disease (AD). Although replacement of dopamine can temporarily alleviate the symptoms of PD patients, it can not prevent the progression of the disease. Increasing evidence has suggested that neuroinflammation significantly contributes to the progress of PD. Therefore, anti-inflammatory therapy could represent a promising neuroprotective intervention with the potential to delay or prevent onset of the disease. This review summarizes several novel potential agents/candidates that might open new avenues for the treatment of PD. In addition to possessing demonstrated anti-inflammatory activities that operate through different molecular mechanisms, these agents exert neuroprotective effects by enhancing the production of neurotrophic factors or interfering with the apoptosis of neurons.
帕金森病(PD)是一种运动系统障碍,源于中脑黑质(SN)中多巴胺能(DAergic)神经元的进行性丧失。它是最常见的神经退行性疾病之一,其发病率仅次于阿尔茨海默病(AD)。虽然多巴胺替代疗法可以暂时缓解 PD 患者的症状,但不能阻止疾病的进展。越来越多的证据表明,神经炎症对 PD 的进展有重要作用。因此,抗炎治疗可能是一种有前途的神经保护干预措施,具有延迟或预防疾病发作的潜力。本综述总结了几种可能为 PD 治疗开辟新途径的新型潜在药物/候选药物。这些药物除了具有通过不同分子机制发挥抗炎作用的特性外,还通过增强神经营养因子的产生或干扰神经元凋亡来发挥神经保护作用。