Muthane U, Yasha T C, Shankar S K
Department of Neurology, National Institutes of Mental Health and Neurosciences, Bangalore, India.
Ann Neurol. 1998 Mar;43(3):283-7. doi: 10.1002/ana.410430304.
The prevalence of Parkinson's disease (PD) is higher in whites than in nonwhites and it increases with advancing age. The pathological hallmarks of PD are loss of pigmented neurons in the substantia nigra pars compacta (SNpc) and presence of Lewy bodies. With increasing age, a similar loss of pigmented neurons in the SNpc has been reported. Hence, age and race possibly play a role in the pathogenesis of PD. The objectives of this study were to count the number of melanized neurons in the SNpc in normal human brains from India and study the change in neuronal count with advancing age and to compare the neuronal counts from this Indian population with counts reported in normal brains from the United Kingdom. Melanized neurons in the SNpc were counted in 84 normal human brains (age range, 5-84 years) in a single 7-microm section at the level of emergence of the oculomotor nerve. In the brains from India, there was no loss of melanized nigral neurons with advancing age. The absolute number of these melanized neurons was about 40% lower than the brains from UK. Despite a low number of melanized nigral neurons in the brains from India, individuals function normally and have dopamine levels comparable with their Western counterparts, suggesting that it is not the absolute number of melanized nigral neurons but the percent loss of nigral neurons that results in dopaminergic deficiency in PD. There is no significant loss of pigmented nigral neurons with age, suggesting that the loss seen in PD is exclusively due to the disease process itself. Indians have a lower prevalence of PD despite having a low count of melanized nigral neurons, suggesting that better protective mechanisms may be present in the Indians to prevent the loss of nigral neurons.
帕金森病(PD)在白人中的患病率高于非白人,且随年龄增长而增加。PD的病理特征是黑质致密部(SNpc)中色素神经元的丧失和路易小体的存在。随着年龄的增长,已有报道称SNpc中出现类似的色素神经元丧失。因此,年龄和种族可能在PD的发病机制中起作用。本研究的目的是统计来自印度的正常人类大脑中SNpc中黑色素化神经元的数量,研究神经元数量随年龄增长的变化,并将该印度人群的神经元数量与英国正常大脑中报道的数量进行比较。在动眼神经出现水平的单个7微米切片中,对84个正常人类大脑(年龄范围5 - 84岁)中的SNpc黑色素化神经元进行计数。在来自印度的大脑中,随着年龄增长,黑色素化的黑质神经元没有丧失。这些黑色素化神经元的绝对数量比来自英国的大脑低约40%。尽管来自印度的大脑中黑色素化的黑质神经元数量较少,但个体功能正常,多巴胺水平与西方同龄人相当,这表明导致PD中多巴胺能缺乏的不是黑色素化黑质神经元的绝对数量,而是黑质神经元的丧失百分比。随着年龄增长,色素性黑质神经元没有明显丧失,这表明在PD中看到 的丧失完全是由于疾病过程本身。尽管黑色素化黑质神经元数量较少,但印度人PD的患病率较低,这表明印度人可能存在更好的保护机制来防止黑质神经元的丧失。