Dopamine D4 receptors modulate brain metabolic activity in the prefrontal cortex and cerebellum at rest and in response to methylphenidate
Journal Article
·
· European Journal of Neuroscience
Methylphenidate (MP) is widely used to treat attention deficit hyperactivity disorder (ADHD). Variable number of tandem repeats polymorphisms in the dopamine D4 receptor (D{sub 4}) gene have been implicated in vulnerability to ADHD and the response to MP. Here we examined the contribution of dopamine D4 receptors (D4Rs) to baseline brain glucose metabolism and to the regional metabolic responses to MP. We compared brain glucose metabolism (measured with micro-positron emission tomography and [{sup 18}F]2-fluoro-2-deoxy-D-glucose) at baseline and after MP (10 mg/kg, i.p.) administration in mice with genetic deletion of the D{sub 4}. Images were analyzed using a novel automated image registration procedure. Baseline D{sub 4}{sup -/-} mice had lower metabolism in the prefrontal cortex (PFC) and greater metabolism in the cerebellar vermis (CBV) than D{sub 4}{sup +/+} and D{sub 4}{sup +/-} mice; when given MP, D{sub 4}{sup -/-} mice increased metabolism in the PFC and decreased it in the CBV, whereas in D{sub 4}{sup +/+} and D{sub 4}{sup +/-} mice, MP decreased metabolism in the PFC and increased it in the CBV. These findings provide evidence that D4Rs modulate not only the PFC, which may reflect the activation by dopamine of D4Rs located in this region, but also the CBV, which may reflect an indirect modulation as D4Rs are minimally expressed in this region. As individuals with ADHD show structural and/or functional abnormalities in these brain regions, the association of ADHD with D4Rs may reflect its modulation of these brain regions. The differential response to MP as a function of genotype could explain differences in brain functional responses to MP between patients with ADHD and healthy controls and between patients with ADHD with different D{sub 4} polymorphisms.
- Research Organization:
- BROOKHAVEN NATIONAL LABORATORY (BNL)
- Sponsoring Organization:
- NATIONAL INSTITUTE ON ALCOHOL ABUSE & ALCOHOLISM
- DOE Contract Number:
- AC02-98CH10886
- OSTI ID:
- 1014321
- Report Number(s):
- BNL--94266-2010-JA
- Journal Information:
- European Journal of Neuroscience, Journal Name: European Journal of Neuroscience Journal Issue: 4 Vol. 32; ISSN 0953-816X
- Country of Publication:
- United States
- Language:
- English
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Sat May 01 00:00:00 EDT 2010
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·
OSTI ID:1041498
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Related Subjects
2-[18F]-fluoro-2-deoxy-d-glucose
59 BASIC BIOLOGICAL SCIENCES
99 GENERAL AND MISCELLANEOUS
BRAIN
CEREBELLUM
DOPAMINE
FUNCTIONALS
GENES
GENETICS
GENOTYPE
GLUCOSE
METABOLISM
MICE
MODULATION
PATIENTS
TOMOGRAPHY
VULNERABILITY
attention deficit hyperactivity disorder
cerebellum
dopamine D4 receptors
methylphenidate
mice
micro-positron emission tomography
prefrontal cortex
59 BASIC BIOLOGICAL SCIENCES
99 GENERAL AND MISCELLANEOUS
BRAIN
CEREBELLUM
DOPAMINE
FUNCTIONALS
GENES
GENETICS
GENOTYPE
GLUCOSE
METABOLISM
MICE
MODULATION
PATIENTS
TOMOGRAPHY
VULNERABILITY
attention deficit hyperactivity disorder
cerebellum
dopamine D4 receptors
methylphenidate
mice
micro-positron emission tomography
prefrontal cortex