Behavioral Pharmacology Laboratory, Department of Psychological & Brain Sciences, University of California, Santa Barbara, CA 93109-9660, USA.
Behavioral Pharmacology Laboratory, Department of Psychological & Brain Sciences, University of California, Santa Barbara, CA 93109-9660, USA.
Pharmacol Biochem Behav. 2018 Dec;175:27-32. doi: 10.1016/j.pbb.2018.09.003. Epub 2018 Sep 7.
Cocaine administration has been shown to produce immediate positive (rewarding) and subsequent negative (anxiogenic) effects in humans and animals. These dual and opposing affective responses have been more difficult to demonstrate with administration of methamphetamine (meth). While animal studies have reliably demonstrated the positive reinforcing effects of the drug, reports of negative aftereffects following acute exposure have been few in number and contradictory in nature. The current research was devised to assess the effects of acute meth using a runway model of self-administration that is uniquely sensitive to both the positive and negative effects of a drug reinforcer in the same animal on the same trial. Male rats were allowed to traverse a straight alley once a day for 16 consecutive days/trials where entry into the goal box resulted in a single IV injection of meth (0.25, 0.5 or 1.0 mg/kg/inj.). The chosen doses were confirmed to be psychoactive as they produced dose-dependent increases in motoric/locomotor activation in these same subjects. The results demonstrated a U-shaped dose-response curve for the reinforcing effects of meth in that the intermediate dose group (0.5 mg/kg) produced the strongest approach behavior in the runway. Unlike other psychomotor stimulants, like cocaine, animals running for IV meth exhibited no evidence of any significant approach-avoidance behaviors reflective of the drug's negative anxiogenic effects. These results suggest that the abuse potential for meth is likely higher than for other shorter-acting psychomotor stimulants and reaffirms the utility of the runway procedure as a screen for a substance's abuse potential.
可卡因给药已被证明在人类和动物中产生即刻的积极(奖励)和随后的消极(焦虑)影响。这些双重和对立的情感反应在给予甲基苯丙胺(冰毒)时更难证明。虽然动物研究可靠地证明了该药物的正强化作用,但急性暴露后出现负后效的报告数量很少,性质也相互矛盾。当前的研究旨在使用自我给药的跑道模型来评估急性冰毒的影响,该模型对药物增强剂在同一动物同一试验中的积极和消极影响具有独特的敏感性。雄性大鼠每天允许在直道上行驶一次,连续 16 天/试验,进入目标箱会导致单次 IV 注射冰毒(0.25、0.5 或 1.0mg/kg/inj.)。所选剂量被确认为具有精神活性,因为它们在相同的受试者中产生了剂量依赖性的运动/运动激活增加。结果表明,冰毒的强化作用呈 U 形剂量反应曲线,即中间剂量组(0.5mg/kg)在跑道上产生了最强的接近行为。与其他精神运动兴奋剂(如可卡因)不同,用于 IV 冰毒的动物没有表现出任何明显的接近回避行为,这些行为反映了药物的消极焦虑作用。这些结果表明,冰毒的滥用潜力可能高于其他作用时间较短的精神运动兴奋剂,并再次证实了跑道程序作为一种筛选物质滥用潜力的工具的效用。