Pickar D, Labarca R, Linnoila M, Roy A, Hommer D, Everett D, Paul S M
Science. 1984 Aug 31;225(4665):954-7. doi: 10.1126/science.6474162.
Plasma-free homovanillic acid, a major metabolite of dopamine, was measured in chronically ill schizophrenic patients both before and during treatment with the antipsychotic phenothiazine, fluphenazine. Neuroleptic treatment was associated with a significant time-dependent decrease in plasma homovanillic acid from pretreatment values, which were significantly elevated when compared with those of age- and sex-matched healthy control subjects. Further, both the absolute concentrations as well as the neuroleptic-induced reductions in plasma homovanillic acid determined over 5 weeks of neuroleptic treatment were statistically significantly correlated with ratings of psychosis and improvement in psychosis, respectively. These findings suggest that the delayed effects of neuroleptic agents on presynaptic dopamine activity may more closely parallel their therapeutic actions than do their immediate effects in blocking postsynaptic dopamine receptors and that a decrease in dopamine "turnover" may be responsible for their antipsychotic effects.
在慢性精神分裂症患者中,于使用抗精神病药物吩噻嗪类的氟奋乃静治疗前及治疗期间,测定了无血浆的高香草酸(多巴胺的主要代谢产物)。抗精神病药物治疗与血浆高香草酸从治疗前水平随时间显著降低相关,治疗前水平与年龄和性别匹配的健康对照受试者相比显著升高。此外,在5周的抗精神病药物治疗期间测定的血浆高香草酸的绝对浓度以及抗精神病药物引起的降低,分别与精神病评分和精神病改善情况在统计学上显著相关。这些发现表明,抗精神病药物对突触前多巴胺活性的延迟作用可能比其阻断突触后多巴胺受体的即时作用更紧密地与其治疗作用平行,并且多巴胺“周转率”的降低可能是其抗精神病作用的原因。