Ahmad S Omar, Park Ji-Hyuk, Stenho-Bittel Lisa, Lau Yuen-Sum
Department of Occupational Therapy Education, University of Kansas Medical Center, Mail Stop 2003, 3901 Rainbow Boulevard, Kansas City, KS 66160, United States.
Neurosci Lett. 2009 Jan 30;450(2):102-5. doi: 10.1016/j.neulet.2008.11.065. Epub 2008 Dec 6.
Loss of dopaminergic neurons in the substantia nigra (A9 cells) and ventral tegmental area (VTA) (A10 cells) has been reported in Parkinson's disease with reference to causing motor and non-motor deficits, although clinical and laboratory animal studies on the degeneration of VTA neurons are less emphasized comparative to the degeneration of substantia nigra neurons. In the present study, we examined the VTA dopaminergic neurons in a chronic mouse model of Parkinson's disease induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine and probenecid at a level showing moderate neurodegeneration and studied the impact of endurance exercise on VTA neurons in this model. In comparison to the normal control animals, the chronic mouse model of Parkinson's disease with moderate neurodegeneration demonstrated a significant reduction of VTA neurons (52% loss), when these animals were kept sedentary throughout the study. Morphologically, the VTA dopaminergic neurons in this model displayed a decrease in cell volume and showed irregular or disparaging axonal and dendritic projections. When the chronic Parkinsonian mice were exercised on a motorized rodent treadmill up to 15m/min, 40 min/day, 5 days/week for 10 and 18 weeks, the total number of VTA dopaminergic neurons were significantly higher than the sedentary Parkinsonian animals. Especially noted with the 18-week exercised Parkinsonian mice, the number of VTA neurons returned to normal range and the cells were densely populated and displayed distinctive axons and dendritic arborization. These results demonstrate that prolonged exercise training is neuroprotective to the dopaminergic neurons in the VTA of the chronic mouse model of Parkinson's disease with moderate neurodegeneration.
帕金森病中,黑质(A9细胞)和腹侧被盖区(VTA)(A10细胞)的多巴胺能神经元缺失与运动和非运动功能缺陷的发生有关,尽管与黑质神经元变性相比,关于VTA神经元变性的临床和实验动物研究较少受到重视。在本研究中,我们在由1-甲基-4-苯基-1,2,3,6-四氢吡啶和丙磺舒诱导的帕金森病慢性小鼠模型中,在中度神经变性水平下检测了VTA多巴胺能神经元,并研究了耐力运动对该模型中VTA神经元的影响。与正常对照动物相比,具有中度神经变性的帕金森病慢性小鼠模型显示VTA神经元显著减少(损失52%),这些动物在整个研究过程中保持久坐不动。形态学上,该模型中的VTA多巴胺能神经元细胞体积减小,轴突和树突投射不规则或有损伤。当慢性帕金森病小鼠在电动啮齿动物跑步机上以15m/min、每天40分钟、每周5天的速度运动10周和18周时,VTA多巴胺能神经元的总数显著高于久坐不动的帕金森病动物。特别值得注意的是,经过18周运动训练的帕金森病小鼠,VTA神经元数量恢复到正常范围,细胞密集分布,并显示出独特的轴突和树突分支。这些结果表明,长期运动训练对中度神经变性的帕金森病慢性小鼠模型VTA中的多巴胺能神经元具有神经保护作用。