Department of Neurological Sciences, Rush University Medical Centre, Chicago, Illinois 60612, USA.
Brain. 2013 Aug;136(Pt 8):2419-31. doi: 10.1093/brain/awt192.
The pace of nigrostriatal degeneration, both with regards to striatal denervation and loss of melanin and tyrosine hydroxylase-positive neurons, is poorly understood especially early in the Parkinson's disease process. This study investigated the extent of nigrostriatal degeneration in patients with Parkinson's disease at different disease durations from time of diagnosis. Brains of patients with Parkinson's disease (n=28) with post-diagnostic intervals of 1-27 years and normal elderly control subjects (n=9) were examined. Sections of the post-commissural putamen and substantia nigra pars compacta were processed for tyrosine hydroxylase and dopamine transporter immunohistochemistry. The post-commissural putamen was selected due to tissue availability and the fact that dopamine loss in this region is associated with motor disability in Parkinson's disease. Quantitative assessments of putaminal dopaminergic fibre density and stereological estimates of the number of melanin-containing and tyrosine hydroxylase-immunoreactive neurons in the substantia nigra pars compacta (both in total and in subregions) were performed by blinded investigators in cases where suitable material was available (n=17). Dopaminergic markers in the dorsal putamen showed a modest loss at 1 year after diagnosis in the single case available for study. There was variable (moderate to marked) loss, at 3 years. At 4 years post-diagnosis and thereafter, there was virtually complete loss of staining in the dorsal putamen with only an occasional abnormal dopaminergic fibre detected. In the substantia nigra pars compacta, there was a 50-90% loss of tyrosine hydroxylase-positive neurons from the earliest time points studied with only marginal additional loss thereafter. There was only a ∼10% loss of melanized neurons in the one case evaluated 1 year post-diagnosis, and variable (30 to 60%) loss during the first several years post-diagnosis with more gradual and subtle loss in the second decade. At all time points, there were more melanin-containing than tyrosine hydroxylase-positive cells. Loss of dopaminergic markers in the dorsal putamen occurs rapidly and is virtually complete by 4 years post-diagnosis. Loss of melanized nigral neurons lags behind the loss of dopamine markers. These findings have important implications for understanding the nature of Parkinson's disease neurodegeneration and for studies of putative neuroprotective/restorative therapies.
黑质纹状体变性的速度,无论是纹状体去神经支配还是黑色素和酪氨酸羟化酶阳性神经元的丧失,在帕金森病早期过程中都知之甚少。本研究调查了不同诊断后时间的帕金森病患者的黑质纹状体变性程度。检查了帕金森病患者(n=28)的脑,这些患者的诊断后间隔为 1-27 年,以及正常老年对照组(n=9)。对后连合壳核和黑质致密部的切片进行酪氨酸羟化酶和多巴胺转运体免疫组织化学处理。选择后连合壳核是因为组织可用性,以及该区域的多巴胺丧失与帕金森病的运动障碍相关。在有合适材料的情况下(n=17),由盲法研究者对壳核多巴胺能纤维密度的定量评估和黑质致密部(总区域和亚区域)中黑色素含量和酪氨酸羟化酶免疫反应性神经元数量的立体学估计进行了评估。在可供研究的单个病例中,在诊断后 1 年时,背侧壳核中的多巴胺能标志物显示出适度丧失。在 3 年时,出现了可变(中度至重度)丧失。在诊断后 4 年及以后,背侧壳核中的染色几乎完全丧失,仅偶尔检测到异常的多巴胺能纤维。在黑质致密部,从最早的研究时间点开始,酪氨酸羟化酶阳性神经元的丧失为 50-90%,此后仅略有额外丧失。在评估的 1 年时,只有 1 例黑质神经元中有约 10%的黑色素丧失,在诊断后最初几年中有可变(30-60%)的丧失,在第二个十年中逐渐且微妙地丧失。在所有时间点,黑色素含量比酪氨酸羟化酶阳性细胞多。背侧壳核中的多巴胺能标志物的丧失迅速发生,在诊断后 4 年内几乎完全丧失。黑色素化黑质神经元的丧失滞后于多巴胺标志物的丧失。这些发现对理解帕金森病神经退行性变的性质以及对潜在神经保护/修复治疗的研究具有重要意义。