Lupien J R, Bray G A
Pharmacol Biochem Behav. 1986 Oct;25(4):733-8. doi: 10.1016/0091-3057(86)90378-3.
Amphetamine, diethylpropion and mazindol were administered to rats in both acute and chronic experiments to measure the changes in purine nucleotide (GDP) binding to the mitochondria from interscapular brown adipose tissue. There was a dose-dependent response to acute treatment with mazindol, but no such effect with diethylpropion. The effects of mazindol and amphetamine were present as early as 3 hours after treatment, and persisted for at least 48 hours, when compared to vehicle-injected rats when all rats were fasted from the time of injection until study. There was no effect when these drugs were added in vitro to mitochondria from brown adipose tissue. Diethylpropion had no effect on GDP binding either in vivo or in vitro at any of the times tested. Following 11 days of treatment with diethylpropion, amphetamine or mazindol, there was a significant increase in purine nucleotide (GDP) binding to mitochondria only in the amphetamine-treated animals. There was no difference in body weight or food intake with any of the three drugs after the third day of chronic treatment. The differences between the effects of these three drugs and those of fenfluramine are discussed in terms of their different central mechanisms of action.
在急性和慢性实验中,给大鼠施用苯丙胺、二乙丙胺苯丙酮和马吲哚,以测量肩胛间棕色脂肪组织线粒体中嘌呤核苷酸(GDP)结合的变化。马吲哚急性治疗呈现剂量依赖性反应,但二乙丙胺苯丙酮没有这种效果。与注射溶媒的大鼠相比,当所有大鼠从注射时起禁食直至研究时,马吲哚和苯丙胺的作用在治疗后3小时就已出现,并持续至少48小时。将这些药物体外添加到棕色脂肪组织的线粒体中时没有效果。在任何测试时间,二乙丙胺苯丙酮在体内或体外对GDP结合均无影响。在用二乙丙胺苯丙酮、苯丙胺或马吲哚治疗11天后,仅在苯丙胺治疗的动物中,嘌呤核苷酸(GDP)与线粒体的结合显著增加。慢性治疗第三天后,这三种药物对体重或食物摄入量均无差异。根据这三种药物与芬氟拉明作用的不同中枢机制,讨论了它们作用效果的差异。