Whether the Subacute MPTP-Treated Mouse is as Suitable as a Classic Model of Parkinsonism.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2023-09-01 Epub Date: 2023-03-13 DOI:10.1007/s12017-023-08740-7
Yue Qi, Ziwei Zhang, Yanning Li, Guojian Zhao, Jinyong Huang, Yi Zhang, Jinhua Xue, Xiaolu Tang
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Abstract

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.

Abstract Image

亚急性MPTP治疗小鼠是否适合作为帕金森病的经典模型。
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MPTP中毒模型因其周期短且与帕金森病相似而备受关注。然而,小鼠亚急性MPMP中毒是否模拟帕金森病的运动和认知障碍仍存在很大争议。因此,本研究在建模后的不同时间点(1、7、14和21天)使用开放视野、旋转杆、Y迷宫和步态分析重新评估了小鼠亚急性MPTP中毒的行为表现。目前的研究结果表明,尽管使用亚急性方案的MPTP治疗小鼠表现出严重的多巴胺能神经元损失和明显的星形胶质细胞增生,但它们没有表现出显著的运动和认知缺陷。此外,坏死标志物混合谱系激酶结构域样(MLKL)在MPTP中毒小鼠的腹侧中脑和纹状体中的表达也显著增加。这显然意味着坏死可能在MPTP诱导的神经退行性变中发挥重要作用。总之,本研究的结果表明,亚急性MPTP中毒小鼠可能不是研究帕金森病的合适模型。然而,它有助于揭示帕金森病的早期病理生理学,并研究早期帕金森病中发生的防止行为缺陷出现的补偿机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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