Chen S D, Zhou X D, Xu D L, Li G W, Tang Q M, Xu X R
Department of Neurology, Renji Hospital.
Chin Med J (Engl). 1991 Sep;104(9):758-63.
After local surgical exposure, we administrated 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) directly into the right common carotid artery of 5 rhesus monkeys. All the monkeys manifested akinesia, rigidity and postural tremor of the contralateral limbs, and spontaneous circling toward the MPTP treated side. These disturbances began to appear 3-4 days after injection, peaking at one month, and continued until the day of sacrifice. After treatment with madopar and apomorphine, marked improvements of the motor impairments appeared and a striking reversal of the direction of rotation away from the MPTP-treated side occurred in a dose-dependent manner. The ipsilateral neurotoxicity was confirmed biochemically by 99% reduction in the caudate-putamen dopamine levels and histologically by selective cell loss in the substantia nigra of the MPTP-treated side. It is concluded that this primate model of hemiparkinsonism is easy to reproduce and life is maintained with good health otherwise. So it may be more feasible for behavioral and pharmacological studies of Parkinson's disease.
在进行局部手术暴露后,我们将1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)直接注入5只恒河猴的右侧颈总动脉。所有猴子均出现对侧肢体运动不能、强直和姿势性震颤,并自发地向MPTP注射侧转圈。这些障碍在注射后3 - 4天开始出现,1个月时达到高峰,并持续到处死当天。在用美多芭和阿扑吗啡治疗后,运动障碍有明显改善,并且以剂量依赖的方式出现了明显的旋转方向反转,即从远离MPTP注射侧的方向转向MPTP注射侧。通过尾状核-壳核多巴胺水平降低99%从生化角度证实了同侧神经毒性,并且通过MPTP注射侧黑质中选择性细胞丢失从组织学角度证实了同侧神经毒性。得出的结论是,这种偏侧帕金森病灵长类动物模型易于复制,并且在其他方面动物健康状况良好。因此,它可能更适合用于帕金森病的行为学和药理学研究。