Tessel R E, Woods J H
Psychopharmacologia. 1975 Sep 17;43(3):239-44. doi: 10.1007/BF00429257.
N-ethyl amphetamine HCl (NEA) and fenfluramine HCl (meta-trifluoromethyl N-ethyl amphetamine) were evaluated as reinforcers in rhesus monkeys that had been previously trained to press a lever using food presentations and cocaine HCl injections as reinforcers. Each daily session consisted of episodic opportunities to obtain reinforcers under a fixed-ratio schedule of 30. A drug period was interpolated between two periods in which lever-press responding was maintained by food presentations. Compared to saline, none of the drugs altered the rate of responding in the food periods which preceded the drug sessions, indicating the absence of residual response-disrupting drug actions from previous sessions. However, NEA and fenfluramine self-injection resulted in dose-related decreases in response rates during the food periods which immediately followed the drug sessions. Cocaine HCl (30 mug/kg/injection) maintained high response rates at over one response/second during the drug periods, as did the same dose of NEA. Doses of 10 and 100 mug/kg/injection of NEA as well as all doses of fenfluramine HCl (10 through 300 mug/kg/injection) maintained rates that were not different from those associated with saline injections. These results substantiate and extend earlier findings with fenfluramine and indicate that its failure to act as a reinforcer is attributable to its meta-trifluoromethyl group.
盐酸N - 乙基苯丙胺(NEA)和盐酸芬氟拉明(间三氟甲基N - 乙基苯丙胺)在恒河猴中被评估为强化物,这些恒河猴先前已接受训练,使用食物呈现和盐酸可卡因注射作为强化物来按压杠杆。每天的实验环节包括按固定比例30获得强化物的间歇性机会。在两个由食物呈现维持杠杆按压反应的阶段之间插入一个药物阶段。与生理盐水相比,在药物阶段之前的食物阶段,没有一种药物改变反应速率,这表明前一阶段不存在残留的干扰反应的药物作用。然而,NEA和芬氟拉明的自我注射导致在紧随药物阶段之后的食物阶段反应速率出现剂量相关的下降。盐酸可卡因(30微克/千克/注射)在药物阶段维持高反应速率,超过每秒一次反应,相同剂量的NEA也是如此。10微克/千克/注射和100微克/千克/注射剂量的NEA以及所有剂量的盐酸芬氟拉明(10至300微克/千克/注射)维持的反应速率与生理盐水注射相关的反应速率没有差异。这些结果证实并扩展了早期关于芬氟拉明的研究发现,并表明其不能作为强化物是归因于其间三氟甲基基团。