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MPTP: A neurotoxin relevant to the pathophysiology of Parkinson's disease: The 1985 George C. Cotzias Lecture

Snyder, Solomon H., D'Amato, Robert J.·1986·Neurology

Abstract

MPTP (N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) elicits selective destruction of nigrostriatal dopamine neurons in humans and animals along with clinical symptoms of parkinsonism. Recent studies clarify mechanisms accounting for this neurotoxicity. MPTP binds with high affinity to monoamine oxidase, which transforms it to the pyridinium MPP+ . MPP+ is selectively concentrated by the dopamine neuronal uptake system. In nigral cells, binding by melanin of MPP+ affords a "depot" release mechanism to maintain prolonged high intracellular concentrations sufficient to destroy cells. PC-12 cells provide a model catecholamine cell culture for screening environmentally occurring substances that may be relevant in the etiology of idiopathic Parkinson's disease.

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Metadata

Authors
Snyder, S. H., & D'Amato, R. J.
Venue
Neurology
Published
1986-02
Volume
36
Issue
2
Pages
250-250
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W2063985177
Cited by
294
References
0
FWCI
31.64
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: MPTP: A neurotoxin relevant to the pathophysiology of Parkinson's disease: The 1985 George C. Cotzias Lecture. https://app.cochat.ai/papers/10.1212/wnl.36.2.250
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Snyder, S. H., & D'Amato, R. J. (1986). MPTP: A neurotoxin relevant to the pathophysiology of Parkinson's disease: The 1985 George C. Cotzias Lecture. Neurology. https://doi.org/10.1212/wnl.36.2.250

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.