## Abstract We used [^11^C]raclopride (RACLO) and positron emission tomography (PET) to study longitudinally striatal dopamine D~2~ receptor binding in nine patients with Parkinson's disease (PD) at an early drug‐naive stage and 3–5 years later, when motor fluctuations had appeared in seven of them
Positron emission tomography demonstrates dopamine D2 receptor supersensitivity in the striatum of patients with early Parkinson's disease
✍ Scribed by Prof. U. K. Rinne; A. Laihinen; J. O. Rinne; K. Naågren; J. Bergman; U. Ruotsalainen
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 836 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0885-3185
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✦ Synopsis
Abstract
Striatal dopamine D~2~ receptor binding was studied in vivo with positron emission tomography in seven patients with early Parkinson's disease using [^11^C]–raclopride. The patients had unilateral symptoms and none of them had received levodopa treatment. The accumulation of [^11^C]–raclopride in the striatum was rapid and reached a steady state at approximately 40 min after injection. The binding of [^11^C]–raclopride was measured in the striatum and cerebellum: The total striatal radioactivity in both hemispheres was counted and the respective striatum/cerebellum ratios were calculated. The striatum/cerebellum ratio of [^11^C]–raclopride binding was significantly (p < 0.01) increased in the hemisphere contralateral to the parkinsonian symptoms as compared with the opposite hemisphere. Thus, this study demonstrates that there is denervation supersensitivity in dopamine D~2~ receptor binding in early Parkinson's disease.
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Striatal dopamine D-1 receptor binding was investigated in vivo with positron emission tomography (PET) in five patients with early Parkinson's disease using ["CI-SCH 23390. All patients had predominantly unilateral symptoms and showed a significant reduction in the accumulation of ["F]-6-F-DOPA in