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Occupancy of dopamine D2 receptors by the atypical antipsychotic drugs risperidone and olanzapine: theoretical implications.

机译:非典型抗精神病药物利培酮和奥氮平对多巴胺D2受体的占用:理论意义。

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RATIONALE: To examine the D2 occupancy of two commonly used antipsychotic medications and relate this to the D2 occupancy by endogenous dopamine in schizophrenia. OBJECTIVES: The aim of this study is to compare the occupancy of striatal D2 receptors by the atypical antipsychotic medications risperidone and olanzapine at fixed dosages and to estimate the effect on D2 occupancy by dopamine as a result of these treatments. METHODS: Seven patients with schizophrenia taking risperidone 6 mg/day and nine patients with schizophrenia taking olanzapine 10 mg/day underwent an [123I]IBZM SPECT scan after 3 weeks of treatment. The specific to non-specific equilibrium partition coefficient (V3") after bolus plus constant infusion of the tracer was calculated as [(striatal activity)/(cerebellar activity)]-1. D2 receptor occupancy was calculated by comparing V3" measured in treated patients to an age-corrected V3" value derived from a group of untreated patients with schizophrenia, previously published, according to the following formula: OCC=1-(V3" treated/V3" drug free). RESULTS: V3" was significantly lower in risperidone treated patients compared with olanzapine treated patients (0.23+/-0.06 versus 0.34+/-0.08, P=-0.01), which translated to a significantly larger occupancy in schizophrenic patients treated with risperidone compared to olanzapine (69+/-8% versus 55 +/-11%, P=0.01). Data from our previous study were used to calculate the occupancy of striatal D2 receptors by antipsychotic medications required to reduce the occupancy of these receptors by endogenous dopamine to control values. In medication-free patients with schizophrenia, the occupancy of striatal D2 receptors by endogenous dopamine is estimated at 15.8%. In healthy controls, the occupancy of striatal D2 receptors by dopamine is estimated at 8.8%. In order to reduce the dopamine occupancy of striatal D2 receptors in patients with schizophrenia to control values, 48% receptor occupancy by antipsychotic medications is required. CONCLUSIONS: These data indicate that the dosage of these medications, found to be effective in the treatment of schizophrenia, reduces DA stimulation of D2 receptors to levels slightly lower than those found in unmedicated healthy subjects.
机译:理由:检查两种常用抗精神病药物的D2占有率,并将其与精神分裂症中内源性多巴胺引起的D2占有率相关。目的:本研究的目的是比较固定剂量的非典型抗精神病药物利培酮和奥氮平对纹状体D2受体的占用率,并评估这些疗法对多巴胺对D2占用率的影响。方法:7例精神分裂症患者服用利培酮6毫克/天,9例精神分裂症患者服用奥氮平10毫克/天,治疗3周后进行[123I] IBZM SPECT扫描。推注加恒定输注示踪剂后的比对非特异性平衡分配系数(V3“)计算为[(纹状体活性)/(小脑活性)]-1。D2受体占用率通过比较治疗组中测得的V3”来计算根据以下公式,由先前发表的一组未经治疗的精神分裂症患者得出的年龄校正后的V3“值:OCC = 1-(V3”已治疗/ V3“不含药物)。结果:V3”显着降低利培酮治疗的患者与奥氮平治疗的患者相比(0.23 +/- 0.06比0.34 +/- 0.08,P = -0.01),这意味着利培酮治疗的精神分裂症患者的入住率明显高于奥氮平(69 +/- 8 %相对于55 +/- 11%,P = 0.01)。我们以前研究的数据用于计算抗精神病药物对纹状体D2受体的占用率,以减少内源多巴胺控制这些值对这些受体的占用。在无药物治疗的精神分裂症患者中,内源性多巴胺对纹状体D2受体的占有率估计为15.8%。在健康对照中,多巴胺对纹状体D2受体的占有率估计为8.8%。为了降低精神分裂症患者纹状体D2受体的多巴胺占有率,以控制其值,抗精神病药物需要48%的受体占有率。结论:这些数据表明,这些药物被发现可有效治疗精神分裂症,其剂量可将DA对D2受体的刺激作用降低至略低于未接受治疗的健康受试者的水平。

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