Emrich H M, Cording C, Pirée S, Kölling A, von Zerssen D, Herz A
Pharmakopsychiatr Neuropsychopharmakol. 1977 Sep;10(5):265-70. doi: 10.1055/s-0028-1094547.
In 20 psychotic patients with frequent hallucinations and/or actual delusional experience a possible antipsychotic action of the opiate antagonist naloxone (N-allyl-noroxymorphone) was investigated, using a double-blind placebo-controlled cross-over design. 18 of these patients were not treated with neuroleptic drugs; 13 suffered from an acute episode of schizophrenia. Psychopathological changes were assessed by the use of the IMPS-scale and of a symptom-specific rating scale (VBS). Intravenous injection of naloxone (in most cases 4.0 mg) induced a reduction of psychotic symptomatology (especially hallucinations) in the majority of patients. Compared with placebo this effect reached statistical significance within 2-7 hours after injection. From this result a possible involvement of endogenous ligands of opiate receptors in the pathogenesis of schizophrenia may be concluded.
在20名经常出现幻觉和/或实际妄想体验的精神病患者中,采用双盲安慰剂对照交叉设计,研究了阿片类拮抗剂纳洛酮(N-烯丙基去甲羟吗啡酮)可能的抗精神病作用。其中18名患者未接受抗精神病药物治疗;13名患有精神分裂症急性发作。通过IMPS量表和症状特异性评定量表(VBS)评估心理病理变化。静脉注射纳洛酮(大多数情况下为4.0毫克)可使大多数患者的精神病症状(尤其是幻觉)减轻。与安慰剂相比,这种效应在注射后2至7小时内具有统计学意义。从这一结果可以推断,阿片受体的内源性配体可能参与了精神分裂症的发病机制。