Rao M L, Brown W A
Nervenklinik, Psychiatrie, Universität Bonn, Federal Republic of Germany.
Psychopharmacology (Berl). 1987;93(2):237-42. doi: 10.1007/BF00179941.
The potential importance of neuroleptic activity measures in the management of schizophrenia warrants attention to the methods for assessing neuroleptic bioactivity and stability of neuroleptic bioactivity over time. We have carried out measurements of serum neuroleptic and prolactin concentrations in 18 schizophrenic patients treated with haloperidol or thioridazine for up to 1 year. Serum neuroleptic levels were measured by a radioreceptor assay using porcine striatum. The lower limit of sensitivity of the assay was 0.6 ng haloperidol/ml, the intra- and interassay coefficients of variation 3 and 9%, respectively. A linear correlation was observed between haloperidol dose (5-30 mg/d) and serum neuroleptic activity (r = 0.706, P less than 0.001) and a curvilinear relationship between thioridazine dose (50-600 mg/d) and serum neuroleptic activity in schizophrenic outpatients. There was a positive correlation between serum neuroleptic and prolactin concentrations for the patients taking haloperidol (r = 0.620, P less than 0.001) or thioridazine (r = 0.542, P less than 0.001). In patients taking a constant dose of haloperidol or thioridazine for up to 1 year serum neuroleptic activity remained stable, suggesting the absence of metabolic tolerance; the observation of a decrease of 38 +/- 16% (mean +/- SD) in serum prolactin concentrations in patients treated with haloperidol but no prolactin decrease with thioridazine suggests that under certain neuroleptic treatment conditions a functional tolerance develops in the tuberoinfundibular dopamine system.
抗精神病药物活性测定在精神分裂症治疗中的潜在重要性,值得关注评估抗精神病药物生物活性的方法以及抗精神病药物生物活性随时间的稳定性。我们对18例接受氟哌啶醇或硫利达嗪治疗长达1年的精神分裂症患者进行了血清抗精神病药物和催乳素浓度的测定。血清抗精神病药物水平采用猪纹状体放射受体分析法进行测定。该分析方法的灵敏度下限为0.6 ng氟哌啶醇/毫升,分析内和分析间变异系数分别为3%和9%。在精神分裂症门诊患者中,观察到氟哌啶醇剂量(5 - 30毫克/天)与血清抗精神病药物活性之间呈线性相关(r = 0.706,P < 0.001),硫利达嗪剂量(50 - 600毫克/天)与血清抗精神病药物活性之间呈曲线关系。服用氟哌啶醇(r = 0.620,P < 0.001)或硫利达嗪(r = 0.542,P < 0.001)的患者,血清抗精神病药物与催乳素浓度之间呈正相关。在服用恒定剂量氟哌啶醇或硫利达嗪长达1年的患者中,血清抗精神病药物活性保持稳定,提示不存在代谢耐受性;观察到服用氟哌啶醇的患者血清催乳素浓度下降了38 ± 16%(均值 ± 标准差),而服用硫利达嗪的患者催乳素未下降,这表明在某些抗精神病药物治疗条件下,结节漏斗多巴胺系统会产生功能性耐受性。