Positron emission tomography after MPTP: observations relating to the cause of Parkinson's disease
- 1 September 1985
- journal article
- case report
- Published by Springer Nature in Nature
- Vol. 317 (6034) , 246-248
- https://doi.org/10.1038/317246a0
Abstract
The dopa analogue 6-fluorodopa (6-FD) used with positron emission tomography (PET) allows in vivo visualization of dopamine and its metabolites in nigrostriatal nerve endings. We have now found abnormal 6-FD scans in four subjects exposed to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). None had parkinsonism. The results suggest subclinical damage to the nigrostriatal pathway. This is the first direct evidence that dopaminergic impairment can exist without clinical deficits. Here we discuss this finding in the context of the hypothesis that Parkinson's disease may stem from clinically silent damage to the substantia nigra, followed by slow attrition of neurones in this region because of its particular vulnerability to cell loss as a normal consequence of ageing.Keywords
This publication has 10 references indexed in Scilit:
- I. MPTP neurotoxicity: An overview and characterization of phases of toxicityLife Sciences, 1985
- Parkinsonism Induced By 1-Methyl-4-Phenyl-1, 2, 3, 6-Tetrahydropyridine (MPTP): Implications for Treatment and the Pathogenesis of Parkinson’s DiseaseCanadian Journal of Neurological Sciences, 1984
- Central Dopaminergic Pathways in Hemiparkinsonism Examined by Positron Emission TomographyCanadian Journal of Neurological Sciences, 1984
- The Cerebral Metabolism of L-DihydroxyphenylalaninePharmacology, 1984
- AETIOLOGY OF PARKINSON'S DISEASEThe Lancet, 1983
- Dopamine visualized in the basal ganglia of living manNature, 1983
- Engineering Developments on the UBC-TRIUMF Modified PETT VI Positron Emission TomographIEEE Transactions on Nuclear Science, 1983
- PETT VIJournal of Computer Assisted Tomography, 1982
- Familial and Acquired Paroxysmal DyskinesiasArchives of Neurology, 1978
- Effects of morphine on striatal dopamine metabolism: Possible mechanism of its opposite effect on locomotor activity in rats and miceEuropean Journal of Pharmacology, 1974