sch-23390 and Obsessive-Compulsive-Disorder

sch-23390 has been researched along with Obsessive-Compulsive-Disorder* in 2 studies

Other Studies

2 other study(ies) available for sch-23390 and Obsessive-Compulsive-Disorder

ArticleYear
Dopamine D(1) receptor binding in the anterior cingulate cortex of patients with obsessive-compulsive disorder.
    Psychiatry research, 2010, Jul-30, Volume: 183, Issue:1

    Functional neuroimaging studies in patients with obsessive-compulsive disorder (OCD) suggest there is a hyperactivation of the anterior cingulate cortex (ACC) during provocation of symptoms and conflict-inhibition tasks. Since dopamine, acting through D(1) receptors is suggested to modulate ACC activity, we hypothesised that there would be an altered D(1) binding potential (BP) in the ACC of OCD patients. Using [(11)C]-SCH23390 and positron emission tomography, we report significantly reduced D(1) BP in seven drug-free OCD patients compared with matched healthy controls. These findings suggest mesocortical dopamine inputs via D(1) receptors may play a role in the aetiology of OCD.

    Topics: Adult; Benzazepines; Brain Mapping; Carbon Isotopes; Dopamine Antagonists; Female; Functional Laterality; Gyrus Cinguli; Humans; Male; Middle Aged; Obsessive-Compulsive Disorder; Positron-Emission Tomography; Protein Binding; Psychiatric Status Rating Scales; Receptors, Dopamine D1

2010
Dopamine D1 receptor binding in the striatum of patients with obsessive-compulsive disorder.
    Journal of affective disorders, 2009, Volume: 114, Issue:1-3

    Obsessive-compulsive disorder (OCD) is a chronic anxiety disorder of unknown aetiology. Psychopharmacological studies have suggested a role for the neurotransmitter serotonin however further evidence for serotonin in the aetiology of OCD is conflicted. The authors used positron emission tomography (PET) to examine the binding of the dopamine D(1) receptor antagonist [(11)C]-SCH23390 to D(1) receptors in the striatum of drug-free OCD patients compared with healthy controls.. Seven drug-free patients (two drug naïve) with OCD and seven age, gender and education matched healthy controls underwent positron emission tomography with [(11)C]-SCH23390. Binding Potentials (BP) at D(1) receptors were calculated for the caudate nucleus and putamen. Correlations between BP values for basal ganglia regions and clinical measures were performed in OCD patients.. The BP for [(11)C]-SCH23390 at D(1) receptors in OCD patients was significantly reduced in both caudate nucleus (0.59+/-0.06 vs 0.88+/-0.06, p<0.05) and putamen (0.89+/-0.06 vs 1.14+/-0.06, p<0.05) compared with healthy controls. No correlations were found between D(1) BP and symptom measures.. The main limitations of this study are the small sample size and the PET methodology which does not allow for disaggregation of Bmax and Kd values for D(1) receptor binding of [(11)C]-SCH23390.. The finding of downregulation of D(1) receptors in the striatum of OCD patients suggests increased nigrostriatal dopaminergic drive in OCD. If confirmed, this finding provides support for trials of novel treatments in OCD based on dopaminergic system blockade.

    Topics: Adult; Aged; Benzazepines; Carbon Radioisotopes; Case-Control Studies; Caudate Nucleus; Dopamine Antagonists; Down-Regulation; Female; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Obsessive-Compulsive Disorder; Positron-Emission Tomography; Psychiatric Status Rating Scales; Putamen; Receptors, Dopamine D1; Young Adult

2009