Winter J C
Psychopharmacology (Berl). 1980;68(2):159-62. doi: 10.1007/BF00432134.
Six rats were trained to discriminate the effects of LSD (100 micrograms/kg) and saline in a two-lever choice task. They were then tested with each of three phenethylamine derivatives, BL-3912 (2,5-dimethoxy-4-methyl-alpha-ethyl-phenethylamine), fenfluramine (N-ethyl-alpha-methyl-m-(trifluoro-methyl)phenethylamine), and Sch-12679 (N-methyl-1-phenyl-7,8-dimethoxy-2,3,4,5-tetra-hydro-3-benzazepine maleate). Fenfluramine and Sch-12679 yielded intermediate results, i.e., responding was not fully appropriate for either training condition while BL-3912 substituted completely for LSD. The LSD-like effects of each of the drugs were antagonized by pretreatment with BC-105, a serotonergic antagonist known to block the stimulus effects of indole and phenethylamine hallucinogens. The present data together with consideration of the known clinical effects of BL-3912, fenfluramine, and Sch-12679 are consistent with the following conclusions: (1) a variety of drugs may substitute in whole or in part for LSD in LSD-trained rats, and (2) even complete substitution of a drug for LSD in the rat is not necessarily associated with the production by that drug of hallucinations in man.
六只大鼠接受训练,在双杠杆选择任务中辨别 LSD(100 微克/千克)和生理盐水的作用。然后用三种苯乙胺衍生物中的每一种对它们进行测试,即 BL - 3912(2,5 - 二甲氧基 - 4 - 甲基 - α - 乙基 - 苯乙胺)、芬氟拉明(N - 乙基 - α - 甲基 - m -(三氟甲基)苯乙胺)和 Sch - 12679(N - 甲基 - 1 - 苯基 - 7,8 - 二甲氧基 - 2,3,4,5 - 四氢 - 3 - 苯并氮杂卓马来酸盐)。芬氟拉明和 Sch - 12679 产生了中间结果,也就是说,反应对于任何一种训练条件都不完全合适,而 BL - 3912 完全替代了 LSD。每种药物的 LSD 样作用都被 BC - 105 预处理所拮抗,BC - 105 是一种已知能阻断吲哚和苯乙胺类致幻剂刺激作用的血清素拮抗剂。目前的数据以及对 BL - 3912、芬氟拉明和 Sch - 12679 已知临床作用的考虑与以下结论一致:(1)在接受 LSD 训练的大鼠中,多种药物可能全部或部分替代 LSD,(2)即使一种药物在大鼠中完全替代了 LSD,也不一定意味着该药物会在人体产生幻觉。