Leith N J, Barrett R J
Psychopharmacology (Berl). 1981;74(1):23-8. doi: 10.1007/BF00431751.
The effects of the d and l isomers of amphetamine on self-stimulation responding were tested following acute and chronic administration. Tolerance and post-drug depression of responding occurred in tests with both isomers, indicating no role for p-hydroxynorephedrine (PHN) which is one of the metabolites of d-amphetamine. In the second experiment, d-amphetamine, methylphenidate and cocaine all produced quantitatively and qualitatively similar effects on self-stimulation responding following acute administration. Following chronic administration of d-amphetamine, animals showed tolerance to all three drugs, indicating cross-tolerance among them. These data are consistent with an hypothesis that tolerance and post-drug depression following chronic amphetamine treatment are the result of decreases in postsynaptic receptor sensitivity, which would lead to a decreased effectiveness of all three drugs, regardless of their pre-synaptic mechanisms.
在急性和慢性给药后,测试了苯丙胺的d型和l型异构体对自我刺激反应的影响。在两种异构体的测试中均出现了耐受性和给药后反应性降低,这表明作为d-苯丙胺代谢产物之一的对羟基去甲麻黄碱(PHN)没有作用。在第二个实验中,d-苯丙胺、哌醋甲酯和可卡因在急性给药后对自我刺激反应均产生了数量和质量上相似的影响。在慢性给予d-苯丙胺后,动物对所有三种药物均表现出耐受性,表明它们之间存在交叉耐受性。这些数据与以下假设一致:慢性苯丙胺治疗后的耐受性和给药后反应性降低是突触后受体敏感性降低的结果,这将导致所有三种药物的有效性降低,而不论其突触前机制如何。