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Striatal presynaptic dopamine function in type 1 alcoholics measured with positron emission tomography
J Tiihonen1, H Vilkman, P Räsänen
1Department of Forensic Psychiatry, University of Kuopio, Finland.
Molecular Psychiatry
|May 13, 1998
Summary
Type 1 alcoholism is not associated with generally decreased dopamine function. Instead, alcoholics showed increased presynaptic dopamine function, potentially a compensatory mechanism, with some individuals exhibiting low function in specific brain regions.
Area of Science:
- Neuroscience
- Psychiatry
- Radiochemistry
Background:
- Previous studies indicated reduced dopamine D2 receptor and transporter densities in late-onset (type 1) alcoholics.
- The hypothesis posited lower striatal presynaptic dopamine function in type 1 alcoholics.
Purpose of the Study:
- To investigate striatal presynaptic dopamine function in type 1 alcoholics using 6-[18F]-FDOPA uptake.
- To determine if dopamine function is decreased in alcoholics compared to controls.
Main Methods:
- Positron emission tomography (PET) imaging with 6-[18F]-FDOPA was used to measure dopamine uptake.
- 10 type 1 alcoholics and 8 matched controls were studied.
- Wisconsin Card Sorting Test (WCST) was administered to assess cognitive function.
Main Results:
- Contrary to the hypothesis, alcoholics exhibited higher mean striatal 6-[18F]-FDOPA uptake than controls, particularly in the left putamen (28% higher) and right caudate (36% higher).
- Elevated uptake in these regions correlated with poorer performance on the WCST, indicating impaired behavioral modification.
- Two patients showed markedly low uptake in the left caudate, suggesting potential heterogeneity within type 1 alcoholism.
Conclusions:
- Type 1 alcoholism is characterized by increased, not decreased, striatal presynaptic dopamine function, possibly as a compensatory response.
- The observed alterations in dopamine function correlate with cognitive deficits in behavioral control.
- Type 1 alcoholism may represent a heterogeneous disorder with varying patterns of presynaptic dopamine dysfunction.