Reta Lila Weston Institute of Neurological Studies, University College London, London, United Kingdom.
Mov Disord. 2011 Jan;26(1):45-50. doi: 10.1002/mds.23340. Epub 2010 Nov 16.
There has been recent interest in the possibility that impaired neurogenesis may contribute to the decline in neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease (PD). We have investigated the effects of commonly used treatments for PD on neural stem cell (NSC) activity in nondemented patients. Postmortem of brain tissue containing the subventricular zone (SVZ) and ependymal layer cells was obtained from 32 nondemented patients with PD. NSC activity was assessed by immunohistochemical staining for RNA-binding protein Musashi1. Regression analyses were then used to identify which clinical factors independently influenced NSC activity. Disease duration was negatively associated with SVZ Musashi1 staining, whereas lifetime levodopa was positively associated in this region. Our findings suggest a positive impact of chronic L-dopa use on the number of NSC in the SVZ of PD patients, which may have relevance for future studies on neuroprotection in neurodegenerative diseases.
最近人们对神经发生受损可能导致阿尔茨海默病和帕金森病(PD)等神经退行性疾病恶化的可能性产生了兴趣。我们研究了常用于治疗 PD 的方法对非痴呆 PD 患者神经干细胞(NSC)活性的影响。从 32 名非痴呆 PD 患者的脑组织中获得包含侧脑室下区(SVZ)和室管膜层细胞的组织。通过免疫组织化学染色 RNA 结合蛋白 Musashi1 评估 NSC 活性。然后使用回归分析来确定哪些临床因素独立影响 NSC 活性。疾病持续时间与 SVZ Musashi1 染色呈负相关,而一生中使用左旋多巴则与该区域呈正相关。我们的研究结果表明,慢性 L-多巴使用对 PD 患者 SVZ 中 NSC 数量有积极影响,这可能对神经退行性疾病中神经保护的未来研究具有重要意义。