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A Rostrocaudal Gradient for Aromatic Acid Decarboxylase in the Human Striatum

Published online by Cambridge University Press:  05 January 2016

E.S. Garnett*
Affiliation:
Department of Nuclear Medicine, McMaster University Medical Centre, Hamilton and the Movement Disorder Clinic, Toronto Western Hospital, Toronto (Dr. Lang)
A.E. Lang
Affiliation:
Department of Nuclear Medicine, McMaster University Medical Centre, Hamilton and the Movement Disorder Clinic, Toronto Western Hospital, Toronto (Dr. Lang)
R. Chirakal
Affiliation:
Department of Nuclear Medicine, McMaster University Medical Centre, Hamilton and the Movement Disorder Clinic, Toronto Western Hospital, Toronto (Dr. Lang)
G. Firnau
Affiliation:
Department of Nuclear Medicine, McMaster University Medical Centre, Hamilton and the Movement Disorder Clinic, Toronto Western Hospital, Toronto (Dr. Lang)
C. Nahmias
Affiliation:
Department of Nuclear Medicine, McMaster University Medical Centre, Hamilton and the Movement Disorder Clinic, Toronto Western Hospital, Toronto (Dr. Lang)
*
Department of Nuclear Medicine, McMaster University Medical Centre, Hamilton, Ontario, Canada L8N 3Z5
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Abstract:

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The local concentration of 6-[18F]fluoro-L-dopa (18F) reflects the activity of aromatic acid decarboxylase (AADC), the enzyme that generates dopamine from its precursor amino acid, L-dopa. In young healthy adults, the local concentration of 18F, and hence AADC activity, is constant in coronal slices taken in a rostrocaudal direction. With increasing age a gradient representing decreasing activity in the putamen develops. This decrease is less marked than was expected from the literature. In five children with primary dystonia, the striatal distribution of 18F resembled that seen in the normal older adults. In established clinical Parkinson's disease the rostrocaudal gradient becomes steep; the putamen is more damaged.

Type
Research Article
Copyright
Copyright © Canadian Neurological Sciences Federation 1987

References

REFERENCES

1.Firnau, G, Garnett, ES, Sourkes, TL, et al. [l8F]fluoro-dopa: a unique gamma emitting substrate for dopa decarboxylase. Experientia 1975; 31: 12541255.CrossRefGoogle Scholar
2.Garnett, ES, Firnau, G, Nahmias, C.Dopamine visualized in the basal ganglia of living man. Nature 1983; 305: 137138.CrossRefGoogle ScholarPubMed
3.Firnau, G, Sood, S, Chirakal, R, et al. Cerebral metabolism of 6-8F]fluoro-L-3,4-dihydroxyphenylalanine in the primate. J Neurochem 1987; 48: 10771082.CrossRefGoogle Scholar
4.Chiueh, CC, Burns, RS, Kopin, IJ, et al. 6-18F-dopa/positron emission tomography visualized degree of damage to brain dopamine in basal ganglia of monkeys with MPTP induced parkinsonism. In: Markey, SP, Castagnoli, N, Kopin, IJ, eds. MPTP-A neurotoxin producing a parkinsonian syndrome. 1986.Google Scholar
5.Chirakal, R, Firnau, G, Garnett, ES. High yield synthesis of 6-[l8F]fluoro-L-dopa. J Nucl Med 1986; 27: 417421.Google Scholar
6.Nahmias, C, Firnau, G, Garnett, ES. Performance characteristics of the McMaster Positron Emission Tomography. I.E.E.E.-NS31 1984; 1: 637639.Google Scholar
7.Gaspar, P, Javoy-Agid, F, Ploska, A, et al. Regional distribution of neurotransmitter synthesizing enzymes in the basal ganglia of human brain. J Neurochem 1980; 34: 278283.CrossRefGoogle ScholarPubMed
8.Nyberg, P, Nordberg, A, Wester, P, et al. Dopaminergic deficiency is more pronounced in putamen than in nucleus caudatus in Parkinson’s disease. Neurochem Pat 1983; 1.Google Scholar
9.Fahn, S, Libsch, LR, Cutler, RW. Monoamines in the human striatum: topographic distribution in normals and Parkinson’s disease and their role in akinesia, rigidity, chorea and tremor. J Neurol Sci 1971; 14: 427455.CrossRefGoogle ScholarPubMed
10.Jerussi, TP, Glick, SD. Drug induced rotation in rats without lesions: behavioural and neurochemical indices of a normal asymmetry in nigrostriatal function. Psychopharmacology 1976; 7: 249260.CrossRefGoogle Scholar
11.Yamamoto, BK, Freed, CR. The trained circling rat: a model for inducing unilateral caudate dopamine metabolism. Nature 1982; 298: 467468.CrossRefGoogle Scholar
12.Hornykeiwicz, O, Kish, SJ, Becker, LE. Brain neurotransmitters in dystonia musculorum deformans.? Eng J Med 1986; 315: 347353.CrossRefGoogle Scholar
13.Leenders, KL, Quinn, N, Frackowiak, RSJ, et al. Brain dopaminergic system studied in patients with dystonia using positron emission tomography. Adv in Neurol 1987 (in press).Google Scholar