Brambilla F, Facchinetti F, Petraglia F, Smeraldi E, Bellodi L, Brancato V, Genazzani A R
Ospedale Psichiatrico Pini, Milano, Italia.
Neuropsychobiology. 1987;18(2):68-73. doi: 10.1159/000118395.
The effects of short- and long-term neuroleptic therapy on peripheral secretion of beta-endorphin (beta-EP) and beta-lipotropin (beta-LPH) were examined in 25 chronic schizophrenic patients. Haloperidol was given to 8 patients for 10 days (group A: 0.1 mg/kg b.w./day) and to another group of 8 patients for 30 days (group B: 10-18 mg/day). The other 9 patients were given a combination of haloperidol (6-30 mg/day) with either chlorpromazine (25-75 mg/day), clotiapine (40-60 mg/day), or fluphenazine decanoate (25-75 mg/month) for 14-18 months (group C). beta-EP and beta-LPH levels were assayed before and after each treatment. Haloperidol plasma levels were assayed in group B patients at the end of treatment. beta-EP mean basal levels were higher in patients than in controls; however, beta-LPH mean basal levels were higher only for group A patients. After treatment, the mean levels did not differ from those prior to therapy in groups A and B, while beta-LPH levels were significantly higher in group C. Level increases or decreases in single patients did not correlate with drug dose or duration of treatment, with baseline peptide levels or with the clinical effects of the various treatments.
对25例慢性精神分裂症患者研究了短期和长期使用抗精神病药物治疗对外周β-内啡肽(β-EP)和β-促脂素(β-LPH)分泌的影响。给8例患者服用氟哌啶醇10天(A组:0.1mg/kg体重/天),给另一组8例患者服用30天(B组:10 - 18mg/天)。另外9例患者服用氟哌啶醇(6 - 30mg/天)与氯丙嗪(25 - 75mg/天)、氯噻平(40 - 60mg/天)或癸酸氟奋乃静(25 - 75mg/月)的组合,持续14 - 18个月(C组)。在每次治疗前后测定β-EP和β-LPH水平。在治疗结束时测定B组患者的氟哌啶醇血浆水平。患者的β-EP平均基础水平高于对照组;然而,仅A组患者的β-LPH平均基础水平较高。治疗后,A组和B组的平均水平与治疗前无差异,而C组的β-LPH水平显著升高。单个患者水平的升高或降低与药物剂量、治疗持续时间、肽的基线水平或各种治疗的临床效果均无相关性。