Owen R R, Gutierrez-Esteinou R, Hsiao J, Hadd K, Benkelfat C, Lawlor B A, Murphy D L, Pickar D
Experimental Therapeutics Branch, National Institute of Mental Health, Bethesda, Md.
Arch Gen Psychiatry. 1993 Aug;50(8):636-44. doi: 10.1001/archpsyc.1993.01820200046005.
To explore serotonin function in patients with schizophrenia during typical and atypical neuroleptic treatment. We hypothesized that clinically relevant doses of the atypical neuroleptic clozapine would attenuate responses to the serotonin agonist m-chlorophenylpiperazine (m-CPP).
m-CPP or placebo was administered intravenously over 90 seconds to patients who had been receiving no medications for at least 3 weeks. m-CPP was also administered during treatment with the typical neuroleptic fluphenazine and the atypical neuroleptic clozapine.
Fifteen inpatients (two women and 13 men) who met DSM-III-R criteria for chronic schizophrenia (n = 13) or schizoaffective disorder (n = 2) participated in the study. Mean age (+/- SD) was 33.8 +/- 8.0 years.
Measures of m-CPP effects included plasma cortisol and prolactin, body temperature, and the Brief Psychiatric Rating Scale (BPRS). The final BPRS total score at approximately 12 weeks of treatment was used to assess response to clozapine.
m-CPP infusion significantly increased plasma cortisol and prolactin levels in drug-free patients. There was a range of behavioral responses while drug-free, but no statistically significant effects on BPRS total or BPRS factor scores. Clozapine treatment significantly blocked neuroendocrine responses to m-CPP, whereas fluphenazine had no effect. Clozapine also appeared to attenuate behavioral responses.
These results demonstrate that clozapine treatment has potent serotonin antagonist effects in patients with schizophrenia. This may be related to clozapine's therapeutic effects since patients with greater cortisol response to m-CPP while drug-free had a better subsequent response to clozapine.
探讨精神分裂症患者在接受传统和非典型抗精神病药物治疗期间的5-羟色胺功能。我们假设,临床相关剂量的非典型抗精神病药物氯氮平会减弱对5-羟色胺激动剂间氯苯哌嗪(m-CPP)的反应。
在90秒内给至少3周未服药的患者静脉注射m-CPP或安慰剂。在使用传统抗精神病药物氟奋乃静和非典型抗精神病药物氯氮平治疗期间也给予m-CPP。
15名住院患者(2名女性和13名男性)参与了研究,他们符合DSM-III-R慢性精神分裂症标准(n = 13)或分裂情感性障碍标准(n = 2)。平均年龄(±标准差)为33.8±8.0岁。
m-CPP效应的指标包括血浆皮质醇和催乳素、体温以及简明精神病评定量表(BPRS)。使用治疗约12周时的最终BPRS总分来评估对氯氮平的反应。
在未服药的患者中,静脉注射m-CPP显著提高了血浆皮质醇和催乳素水平。在未服药时存在一系列行为反应,但对BPRS总分或BPRS因子评分无统计学显著影响。氯氮平治疗显著阻断了对m-CPP的神经内分泌反应,而氟奋乃静则无此作用。氯氮平似乎还减弱了行为反应。
这些结果表明,氯氮平治疗对精神分裂症患者具有强大的5-羟色胺拮抗作用。这可能与氯氮平的治疗效果有关,因为未服药时对m-CPP皮质醇反应较大的患者随后对氯氮平的反应更好。