Elevated Putamen D 2 Receptor Binding Potential in Major Depression With Motor Retardation: An [ 11 C]Raclopride Positron Emission Tomography Study
Abstract
OBJECTIVE: Several antidepressants raise striatal dopamine, but the role of striatal dopamine during major depressive episodes is unclear. Striatal [(11)C]raclopride binding potential measured with positron emission tomography is an index of D(2) type receptors and is sensitive to extracellular dopamine levels (higher D(2) binding potential occurs when dopamine is lower). It was hypothesized that putamen D(2) binding potential would be higher during major depressive episodes featuring motor retardation. METHOD: Drug-free, nonsmoking subjects experiencing a major depressive episode (N=21) underwent [(11)C]raclopride PET imaging as did 21 healthy age-matched comparison subjects. Motor retardation was measured with the finger tapping test. RESULTS: The depressed subjects exhibiting motor retardation had significantly higher D(2) binding potential in both the left and right putamen than did healthy subjects, and putamen D(2) binding potential correlated significantly with motor speed in the depressed subjects. CONCLUSIONS: The results argue that extracellular dopamine is lower in subjects experiencing a major depressive episode that features motor retardation. This depression subtype should preferentially benefit from dopamine-increasing medications and should be targeted in future clinical trials of dopamine reuptake inhibitors.
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Molecular-imaging studies of DA signaling in MDD indicate increased D2 receptor binding in the basal ganglia, striatum, and putamen, whereas other studies report lower or no difference in striatal D2 transporter binding potential.
“These studies have indicated increased D2 receptor binding in the basal ganglia [257], striatum [258,259], and putamen [260], whereas other studies have reported lower [261] or no difference [259,262,263] in striatal D2 transporter binding potential.”
From Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings (2012) · cites this paper as [260]
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References 40 · Cited by 160
- Authors
- Meyer, J. H., McNeely, H. E., Sagrati, S., Boovariwala, A., Martin, K., Verhoeff, N. P. L. G., Wilson, A. A., & Houle, S.
- Affiliations
- Centre for Addiction and Mental Health (CA)
- Venue
- American Journal of Psychiatry
- Published
- 2006-09
- Volume
- 163
- Issue
- 9
- Pages
- 1594-1602
- ISSN
- 0002-953X (ISSN-L)
- 1535-7228
- OpenAlex
- W2061951979
- Cited by
- 160
- References
- 40
- Citations by year
- 2026: 6 · 2025: 4 · 2024: 4 · 2023: 4 · 2022: 3 · 2021: 5 · 2020: 4 · 2019: 4 · 2018: 5 · 2017: 12 · 2016: 11 · 2015: 5 · 2014: 11 · 2013: 12 · 2012: 16
- FWCI
- 6.68
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Keywords
- major depressive disorder, motor retardation, putamen, striatal dopamine, [11C]raclopride PET, finger tapping test, motor speed, dopamine reuptake inhibitors, depression subtypes
- MeSH terms
- Adult, Age Factors, Carbon Radioisotopes, Corpus Striatum, Major Depressive Disorder, Dopamine, Female, Homovanillic Acid, Humans, Functional Laterality, Male, Neuropsychological Tests, Putamen, Sex Factors, Receptors, Dopamine D2, Motor Skills Disorders, Raclopride, Positron-Emission Tomography
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