Barrett A M, McSharry L
J Pharm Pharmacol. 1975 Dec;27(12):889-95. doi: 10.1111/j.2042-7158.1975.tb10243.x.
Iproniazid was found to reduce food consumption in fasting rats. Combined treatment of iproniazid with tryptophan resulted in a significantly greater anorexic action whilst tryptophan alone had no effect on food consumption. Iproniazid treatment was associated with a significant increase in brain 5-hydroxytryptamine (5-HT) concentration but in association with tryptophan higher brain 5-HT concentrations were recorded. The anorexic action of the iproniazid-tryptophan combination was antagonized in a dose-dependent fashion by methysergide. Equivalent levels of anorexia induced by fenfluramine and mazindol were similarly antagonized by methysergide in a dose-related manner. The results suggest a common role of 5-HT in the inhibition of eating behaviour in fasting rats when anorexia is induced by iproniazid, fenfluramine or mazindol, sensitive to a specific 5-HT antagonist.
发现异烟酰异丙肼可减少禁食大鼠的食物摄入量。异烟酰异丙肼与色氨酸联合治疗导致厌食作用显著增强,而单独使用色氨酸对食物摄入量没有影响。异烟酰异丙肼治疗与大脑5-羟色胺(5-HT)浓度显著升高有关,但与色氨酸联合使用时,大脑5-HT浓度更高。异烟酰异丙肼-色氨酸组合的厌食作用被麦角新碱以剂量依赖性方式拮抗。芬氟拉明和马吲哚诱导的同等程度厌食症同样被麦角新碱以剂量相关方式拮抗。结果表明,当异烟酰异丙肼、芬氟拉明或马吲哚诱导厌食时,5-HT在抑制禁食大鼠的进食行为中起共同作用,且对特定的5-HT拮抗剂敏感。