Schechter M D
Department of Pharmacology, Northeastern Ohio Universities College of Medicine, Rootstown 44272.
Psychopharmacology (Berl). 1990;101(1):126-31. doi: 10.1007/BF02253729.
The drug discrimination paradigm was used to evaluate in rats the ability of the discriminate response to either 0.8 mg/kg d-amphetamine or 0.8 mg/kg l-cathinone to generalize to 2.4-6.0 mg/kg of the active cathinone metabolite d-norpseudoephedrine, also known as cathine. When tested 24 h after vehicle administration, cathine generalized in a dose-related fashion in rats (n = 6) trained with cathinone (ED50 = 3.03 mg/kg) and in rats (n = 8) trained with amphetamine (ED50 = 2.93 mg/kg). In contrast, when cathine was tested 24 h after the administration of either amphetamine or cathinone, it produced significantly decreased discriminative performance. The possibility that this acute tolerance may have been produced by release, and subsequent depletion, of brain dopamine was tested by pretreating rats with the dopamine release inhibitor CGS 10746B. When CGS 10746B was administered prior to cathinone it significantly decreased cathinone discrimination. In addition, acute tolerance to cathine at 24 h after vehicle-cathinone co-administration was reversed when cathine was tested 24 h after CGS 10746B-cathinone co-administration. The results suggest that cathinone-produced discriminative stimulus, as well as the acute tolerance to cathine, may be dopaminergically mediated.
药物辨别范式用于评估大鼠对0.8毫克/千克右旋苯丙胺或0.8毫克/千克左旋卡西酮的辨别反应能力,是否能泛化到活性卡西酮代谢物2.4 - 6.0毫克/千克的去甲伪麻黄碱(也称为去甲麻黄碱)。在用卡西酮训练的大鼠(n = 6)和用苯丙胺训练的大鼠(n = 8)中,在给予赋形剂24小时后进行测试时,去甲麻黄碱以剂量相关的方式泛化。(用卡西酮训练的大鼠的半数有效剂量(ED50)= 3.03毫克/千克,用苯丙胺训练的大鼠的半数有效剂量(ED50)= 2.93毫克/千克)。相比之下,在给予苯丙胺或卡西酮24小时后测试去甲麻黄碱时,它产生的辨别性能显著下降。通过用多巴胺释放抑制剂CGS 10746B预处理大鼠,来测试这种急性耐受性是否可能是由脑多巴胺的释放及随后的耗竭所产生的。当在卡西酮之前给予CGS 10746B时,它显著降低了卡西酮辨别能力。此外,当在CGS 10746B与卡西酮共同给药24小时后测试去甲麻黄碱时,在赋形剂与卡西酮共同给药24小时后对去甲麻黄碱的急性耐受性得到了逆转。结果表明,卡西酮产生的辨别刺激以及对去甲麻黄碱的急性耐受性可能是由多巴胺能介导的。