Department of Anatomy and Neuroscience, University College Cork, Cork, Ireland.
Prog Neurobiol. 2009 Nov;89(3):277-87. doi: 10.1016/j.pneurobio.2009.08.001. Epub 2009 Aug 15.
Parkinson's disease (PD) is characterised by degeneration of dopaminergic neurons in the substantia nigra pars compacta (SNpc). Inflammation may be associated with the neuropathology of PD due to the following accumulating evidence: excessive microglial activation and increased levels of the pro-inflammatory cytokines tumour necrosis factor-alpha and interleukin-1beta in the SNpc of patients with PD; the emergence of PD-like symptoms following influenza infection; the increased susceptibility to PD associated with bacterial vaginosis; the presence of inflammatory mediators and activators in animal models of PD; the ability of anti-inflammatory drugs to decrease susceptibility to PD; and the emerging possibility of the use of microglial activation inhibitors as a therapy in PD. In this review, we will discuss the role of inflammation in PD. We will focus on the influence of microglia in the pathogenesis of PD and discuss potential therapeutic interventions for PD, that target microglia.
帕金森病(PD)的特征是黑质致密部(SNpc)中的多巴胺能神经元退化。由于以下累积的证据,炎症可能与 PD 的神经病理学有关:帕金森病患者 SNpc 中过度的小胶质细胞激活和促炎细胞因子肿瘤坏死因子-α和白细胞介素-1β水平升高;流感感染后出现 PD 样症状;细菌性阴道炎与 PD 相关的易感性增加;PD 动物模型中存在炎症介质和激活剂;抗炎药物降低 PD 易感性的能力;以及使用小胶质细胞激活抑制剂作为 PD 治疗方法的可能性不断出现。在这篇综述中,我们将讨论炎症在 PD 中的作用。我们将重点讨论小胶质细胞在 PD 发病机制中的影响,并讨论针对小胶质细胞的 PD 潜在治疗干预措施。