In vitro Toxicology and Biomedicine, Department of Biology, University of Konstanz, D-78457 Konstanz, Germany.
German Center for Neurodegenerative Diseases (DZNE), Sigmund-Freud-Strasse 27, D-53127 Bonn, Germany.
Trends Pharmacol Sci. 2017 Jun;38(6):541-555. doi: 10.1016/j.tips.2017.03.010. Epub 2017 Apr 23.
The neurotoxicant 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) causes a Parkinson's disease (PD)-like syndrome by inducing degeneration of nigrostriatal dopaminergic neurons. Studies of the MPTP model have revealed the pathomechanisms underlying dopaminergic neurodegeneration and facilitated the development of drug treatments for PD. In this review, we provide an update on MPTP bioactivation and biodistribution, reconcile the distinct views on energetic failure versus reactive oxygen species (ROS) formation as main drivers of MPTP-induced neurodegeneration, and describe recently identified intrinsic features of the nigrostriatal system that make it particularly vulnerable to MPTP. We discuss these new perspectives on the endogenous tipping points of tissue homeostasis and the drivers responsible for vicious cycles in relation to their relevance for the development of novel intervention strategies for PD.
神经毒素 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)通过诱导黑质纹状体多巴胺能神经元变性引起帕金森病(PD)样综合征。MPTP 模型的研究揭示了多巴胺能神经退行性变的发病机制,并促进了 PD 药物治疗的发展。在这篇综述中,我们提供了关于 MPTP 生物活化和生物分布的最新信息,调和了能量衰竭与活性氧(ROS)形成作为 MPTP 诱导的神经退行性变主要驱动因素的不同观点,并描述了最近发现的黑质纹状体系统的内在特征,这些特征使其特别容易受到 MPTP 的影响。我们讨论了这些关于组织内稳态的内源性临界点和导致恶性循环的驱动因素的新观点,以及它们与开发 PD 新干预策略的相关性。