Fuller R W, Perry K W, Molloy B B
J Pharmacol Exp Ther. 1975 Jun;193(3):793-803.
3-(p-Trifluoromethylphenoxy)-N-methyl-3-phenylpropylamine (Lilly 110140), when injected into rats at i.p. doses of 1 to 10 mg/kg, prevented the lowering of brain serotonin by 4-chloroamphetamine. The duration of 110140 action was very long, significant antagonism of 4-chloroamphetamine action being apparent still at 48 hours after a single dose of 10 mg/kg of 110140. The N,N-dimethyl tertiary amine derivative was as effective as 110140 itself in antagonizing serotonin depletion by 4-chloroamphetamine, but other structurally related compounds has less activity or were inactive. Likewise, six tricyclic antidepressant drugs injected at 10 mg/kg i.p. did not antagonize the action of 4-chloroamphetamine. When injected into rats whose brain serotonin levels had already been depleted by 3-hour pretreatment with 4-chloroamphetamine, 110140 terminated the action of 4-chloroamphetamine and permitted serotonin levels to return to normal. Lilly 110140 did not antagonize the depletion of brain serotonin or norepinephrine by reserpine, which implies that reserpine does not require the membrane pump for entry into the neuron. The depletion of brain serotonin, but not norepinephrine, by alpha-ethyl-3-hydroxy-4-methylphenethylamine (H75/12) was blocked by 110140. In contrast to chlorimipramine, 110140 did not antagonize the depletion of norepinephrine levels in heart and spleen by 6-hydroxydopamine. The data suggest that 110140 is a specific drug for inhibiting uptake into serotoninergic neurons in the brain.
3 -(对-三氟甲基苯氧基)-N -甲基-3 -苯基丙胺(礼来110140),以1至10毫克/千克的腹腔注射剂量注入大鼠时,可防止4 -氯苯丙胺降低脑血清素水平。110140的作用持续时间很长,单次注射10毫克/千克的110140后48小时,对4 -氯苯丙胺作用的显著拮抗作用仍然明显。N,N -二甲基叔胺衍生物在拮抗4 -氯苯丙胺引起的血清素耗竭方面与110140本身一样有效,但其他结构相关的化合物活性较低或无活性。同样,以10毫克/千克腹腔注射的六种三环抗抑郁药也不能拮抗4 -氯苯丙胺的作用。当注入经4 -氯苯丙胺预处理3小时后脑血清素水平已被耗尽的大鼠体内时,110140可终止4 -氯苯丙胺的作用,并使血清素水平恢复正常。礼来110140不能拮抗利血平引起的脑血清素或去甲肾上腺素的耗竭,这意味着利血平进入神经元不需要膜泵。110140可阻断α-乙基-3 -羟基-4 -甲基苯乙胺(H75/12)引起的脑血清素而非去甲肾上腺素的耗竭。与氯米帕明不同,110140不能拮抗6 -羟基多巴胺引起的心脏和脾脏中去甲肾上腺素水平的耗竭。数据表明,110140是一种特异性药物,可抑制脑内血清素能神经元的摄取。