衰老与黑质纹状体多巴胺系统:一项非人类灵长类动物研究。

I Irwin, L E DeLanney, T McNeill, P Chan, L S Forno, G M Murphy, D A Di Monte, M S Sandy, J W Langston
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摘要

本研究检测了年轻、中年和老年松鼠猴黑质纹状体多巴胺系统的神经化学、形态学和功能标志物。随着年龄的增长,运动活动显著减少。与年龄相关的显著多巴胺缺失发生在黑质(70%)和壳核(30%),但在尾状核中没有。运动活动的减少和壳核多巴胺的减少之间有很强的相关性。然而,黑质纹状体多巴胺丢失似乎不是与年龄相关的多巴胺能神经元丢失的结果,因为酪氨酸免疫反应细胞的数量在三个年龄组之间没有显着差异。这些结果表明,衰老的松鼠猴证明了与年龄相关的黑质纹状体多巴胺的损失被认为发生在人类身上,并将这种非人类灵长类动物确定为进一步研究与年龄相关的黑质纹状体多巴胺系统下降的潜在机制和功能后果的有用模型。此外,壳核而非尾状核中多巴胺的选择性损失与帕金森病(一种与年龄相关的神经退行性疾病)中观察到的区域脆弱性相似,这提高了正常衰老与该疾病发展之间关系的可能性。最后,由于酪氨酸羟化酶(TH)阳性细胞的数量随着年龄的增长而保持不变,这些结果提出了旨在增加多巴胺浓度的治疗策略可能对老年人有益的可能性。
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Aging and the nigrostriatal dopamine system: a non-human primate study.

The present study examined neurochemical, morphological and functional markers of the nigrostriatal dopamine system in young, intermediate-aged and old squirrel monkeys. Striking reductions in motoric activity were observed with advancing age. significant age-related loss of dopamine occurred in the substantia nigra (70%) and the putamen (30%) but not in the caudate. There was a strong correlation between the reductions in motoric activity and the loss of putamen dopamine. However, nigrostriatal dopamine loss did not appear to be the consequence of age-related loss of dopaminergic nigral neurons since the number of tyrosine immunoreactive cells was not significantly different among the three age groups. These results suggest that the aging squirrel monkey demonstrates the age-related loss of nigrostriatal dopamine thought to occur in humans and identify this non-human primate as a useful model to further investigate the underlying mechanism(s) and functional consequences of age-related decline of the nigrostriatal dopamine system. In addition, the selective loss of dopamine in the putamen but not the caudate parallels the regional vulnerability observed in Parkinson's disease, an age-related neurodegenerative disorder, raising the possibility of a relationship between normal aging and the development of this disease. Finally, because the number of tyrosine hydroxylase (TH) positive cells remains constant with age, these results raise the possibility that therapeutic strategies aimed at increasing dopamine concentrations may benefit elderly individuals.

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