Department of Human Anatomy, School of Basic Medical Sciences, Gannan Medical University, Harmonious Avenue, Zhang Gong District, Ganzhou, 341000, China.
Department of Pathophysiology, School of Basic Medical Sciences, Gannan Medical University, Harmonious Avenue, Zhang Gong District, Ganzhou, 341000, China.
Neuromolecular Med. 2023 Sep;25(3):360-374. doi: 10.1007/s12017-023-08740-7. Epub 2023 Mar 13.
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) mice model is one of the most common animal models for Parkinson's disease (PD). It is classified into three types: acute, subacute, and chronic intoxication models. The subacute model has attracted much attention for its short period and similarity to PD. However, whether subacute MPTP intoxication in mouse mimics the movement and cognitive disorders of PD still remains highly controversial. Therefore, the present study reassessed the behavioral performances of subacute MPTP intoxication in mice using open field, rotarod, Y maze, and gait analysis at different time points (1, 7, 14, and 21 days) after modeling. Results of the current study showed that although MPTP-treated mice using subacute regimen showed severe dopaminergic neuronal loss and evident astrogliosis, they failed to display significant motor and cognitive deficits. Besides, expression of mixed lineage kinase domain-like (MLKL), a marker of necroptosis, was also significantly increased in the ventral midbrain and striatum of MPTP-intoxicated mice. This evidently implies that necroptosis may play an important role in MPTP-induced neurodegeneration. In conclusion, the findings of the present study suggest that subacute MPTP-intoxicated mice may not be a suitable model for studying parkinsonism. However, it can help in revealing the early pathophysiology of PD and studying the compensatory mechanisms which occur in early PD that prevent the emergence of behavioral deficits.
1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)小鼠模型是帕金森病(PD)最常见的动物模型之一。它分为三种类型:急性、亚急性和慢性中毒模型。亚急性模型因其周期短且与 PD 相似而引起了广泛关注。然而,亚急性 MPTP 中毒在小鼠中是否模拟 PD 的运动和认知障碍仍然存在很大争议。因此,本研究在建模后不同时间点(1、7、14 和 21 天)使用旷场、转棒、Y 迷宫和步态分析重新评估了亚急性 MPTP 中毒小鼠的行为表现。本研究结果表明,尽管使用亚急性方案处理的 MPTP 处理的小鼠显示出严重的多巴胺能神经元丧失和明显的星形胶质细胞增生,但它们没有表现出明显的运动和认知缺陷。此外,坏死性凋亡的标志物混合谱系激酶结构域样蛋白(MLKL)在 MPTP 中毒小鼠的中脑腹侧和纹状体中的表达也明显增加。这显然表明坏死性凋亡可能在 MPTP 诱导的神经退行性变中起重要作用。总之,本研究的结果表明,亚急性 MPTP 中毒的小鼠可能不是研究帕金森病的合适模型。然而,它可以帮助揭示 PD 的早期病理生理学,并研究早期 PD 中发生的代偿机制,这些机制可以防止行为缺陷的出现。