Ross D L, Klykylo W M, Hitzemann R
Department of Neurology, University of Cincinnati, Ohio.
Pediatr Neurol. 1987 Mar-Apr;3(2):83-6. doi: 10.1016/0887-8994(87)90032-4.
Fenfluramine therapy has been reported to improve behavior in infantile autism and has been associated with a decrease in abnormally increased blood serotonin content. The primary central effect has not been proved to be serotonergic. Beta-endorphin is involved in the anorexic effect of fenfluramine and may play a role in autism. Nine children with infantile autism were treated with fenfluramine in double-blind, placebo-crossover design. Transient anorexia was the only adverse effect. Autistic behavior was reported to improve in three patients, but objective psychometric tests were unchanged. Beta-endorphin-like immunoreactivity was determined in lumbar cerebrospinal fluid of patients during and before or after treatment with fenfluramine and then was compared to normal controls. Beta-endorphin was elevated significantly in the baseline autistic group (p less than .005) and was reduced toward control values during fenfluramine treatment. The results are consistent with a role for beta-endorphin in infantile autism and in the mechanism of fenfluramine treatment.
据报道,芬氟拉明疗法可改善婴儿自闭症患者的行为,并与异常升高的血液血清素含量降低有关。其主要中枢效应尚未被证明是血清素能的。β-内啡肽参与了芬氟拉明的厌食作用,可能在自闭症中起作用。采用双盲、安慰剂交叉设计,对9名婴儿自闭症患儿进行了芬氟拉明治疗。短暂性厌食是唯一的不良反应。据报道,3名患者的自闭症行为有所改善,但客观心理测量测试结果未变。在患者接受芬氟拉明治疗期间以及治疗前或治疗后,测定其腰椎脑脊液中的β-内啡肽样免疫反应性,然后与正常对照组进行比较。在基线自闭症组中,β-内啡肽显著升高(p<0.005),在芬氟拉明治疗期间降至对照值。这些结果与β-内啡肽在婴儿自闭症及芬氟拉明治疗机制中的作用一致。