首页> 外文期刊>European archives of psychiatry and clinical neuroscience >Dual-isotope SPECT imaging of striatal dopamine: a comparative study between never-treated and haloperidol-treated first-episode schizophrenic patients.
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Dual-isotope SPECT imaging of striatal dopamine: a comparative study between never-treated and haloperidol-treated first-episode schizophrenic patients.

机译:纹状体多巴胺的双同位素SPECT成像:从未治疗和氟哌啶醇治疗的首发精神分裂症患者的比较研究。

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摘要

The aim of this dual-isotope SPECT imaging study was to evaluate striatal dopamine transporter (DAT) and D2 receptor availability in first-episode never-treated and haloperidol-treated schizophrenic patients and whether the availability is associated with psychopathology. Twenty-four inpatients with a first acute schizophrenic episode were enrolled in the study; 12 of these patients were treated with haloperidol for 2 weeks before dual-isotope SPECT was performed, whereas the other 12 patients underwent the SPECT evaluation directly after enrollment. Twelve healthy control persons were also recruited and evaluated with the dual-isotope SPECT protocol. Psychopathology was assessed by the Positive and Negative Syndrome Scale and other scales. D2-radioligand binding did not differ between drug-na?ve patients and the control group but was significantly lower in the haloperidol-treated group. DAT availability was also significantly lower in the haloperidol patients than in the other two groups and differed significantly between drug-na?ve, positive-syndrome-type patients and healthy controls. The data obtained with the new dual-isotope SPECT technique reveal a direct effect of haloperidol at the D2 and DAT receptor level.
机译:这项双同位素SPECT成像研究的目的是评估从未接受过治疗和氟哌啶醇治疗的精神分裂症患者的纹状体多巴胺转运蛋白(DAT)和D2受体的有效性,以及有效性是否与心理病理学相关。该研究招募了24名首次出现急性精神分裂症发作的住院患者。这些患者中有12名在进行双同位素SPECT治疗之前接受了氟哌啶醇治疗2周,而其他12名患者在入组后立即接受了SPECT评估。还招募了十二名健康对照者,并用双同位素SPECT方案进行了评估。通过阳性和阴性综合征量表和其他量表评估心理病理学。初次接受药物治疗的患者与对照组之间的D2-放射性配体结合没有差异,但是在氟哌啶醇治疗组中则明显较低。氟哌啶醇患者的DAT可用性也显着低于其他两组,并且初次使用毒品,阳性综合征型患者和健康对照组之间的DAT可用性也存在显着差异。用新的双同位素SPECT技术获得的数据揭示了氟哌啶醇在D2和DAT受体水平上的直接作用。

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