Brown A S, Gewirtz G, Harkavy-Friedman J, Cooper T, Brébion G, Amador X F, Malaspina D, Gorman J M
Department of Psychiatry, College of Physicians and Surgeons of Columbia University, New York State Psychiatric Institute, New York, USA.
Neuropsychopharmacology. 1997 Nov;17(5):317-25. doi: 10.1016/S0893-133X(97)00073-0.
We conducted a within-subject comparison of the effects of clozapine and haloperidol on plasma levels of neurotransmitters and metabolites, and related changes in specific plasma neurochemicals with clozapine response. The subjects were 14 inpatients with schizophrenia or schzoaffective disorder, who were refractory to haloperidol and at least one other typical antipsychotic medication. Subjects underwent, in the following order: a 6-week "fixed, flexible dose" haloperidol trial, followed by a 2-4 week medication-free phase, and a 6-week clozapine trial. Plasma levels of norepinephrine (NE), homovanillic acid (HVA), and 3-methoxy-4-hydroxyphenylglycol (MHPG), and objective clinical ratings of total, positive, negative, and depressive symptoms were obtained at the end of each phase. As expected, we found a substantial increase of plasma NE with clozapine but not with haloperidol. However, the increase in NE was not associated with improvement in total or positive symptomatology. There was some evidence for an association between improvement in negative symptoms and increased HVA on clozapine, as well as diminished HVA during the medication-free phase. The implications of these data for understanding the mechanisms of action of clozapine are discussed.
我们对氯氮平和氟哌啶醇对神经递质及代谢产物血浆水平的影响进行了受试者自身对照比较,并将特定血浆神经化学物质的相关变化与氯氮平反应进行关联。受试者为14名患有精神分裂症或分裂情感性障碍的住院患者,他们对氟哌啶醇及至少一种其他典型抗精神病药物治疗无效。受试者按以下顺序接受试验:为期6周的“固定、灵活剂量”氟哌啶醇试验,随后是为期2 - 4周的停药期,以及为期6周的氯氮平试验。在每个阶段结束时获取去甲肾上腺素(NE)、高香草酸(HVA)和3 - 甲氧基 - 4 - 羟基苯乙二醇(MHPG)的血浆水平,以及对总体、阳性、阴性和抑郁症状的客观临床评分。正如预期的那样,我们发现氯氮平可使血浆NE大幅升高,而氟哌啶醇则无此作用。然而,NE的升高与总体或阳性症状的改善无关。有一些证据表明,氯氮平治疗时阴性症状的改善与HVA升高有关,且在停药期HVA降低。本文讨论了这些数据对于理解氯氮平作用机制的意义。