Katz J L, Prada J A, Goldberg S R
Preclinical Pharmacology Branch, NIDA Addiction Research Center, Baltimore, MD 21224.
Pharmacol Biochem Behav. 1988 Feb;29(2):429-32. doi: 10.1016/0091-3057(88)90181-5.
Effects of the adenosine analogs R-N6-phenylisopropyl-adenosine (R-PIA) and 5'-N-ethylcarboxamidoadenosine (NECA), alone and in combination with caffeine, were studied in squirrel monkeys trained to respond under multiple fixed-interval fixed-ratio schedules of reinforcement. Both drugs produced dose-related decreases in rates of responding, with little difference between effects in the two components. NECA was about ten times more potent than R-PIA in producing these effects, the order of potency suggests that these effects may be mediated by actions at A2-adenosine receptors. Effects of either drug were antagonized by caffeine. Caffeine when administered alone increased rates of responding. The increases in response rates produced by caffeine were altered by R-PIA only at doses of R-PIA that alone decreased response rates. Effects of caffeine were either enhanced or attenuated by doses of NECA that were inactive when administered alone. These results do not support the notion that increases in rates of behavior, e.g., psychomotor-stimulant effects, produced by caffeine are due to its antagonist actions at adenosine receptors.
在经过训练能在多种固定间隔固定比率强化程序下做出反应的松鼠猴身上,研究了腺苷类似物R-N6-苯基异丙基腺苷(R-PIA)和5'-N-乙基甲酰胺基腺苷(NECA)单独使用以及与咖啡因联合使用的效果。两种药物均使反应率出现剂量相关的下降,两种成分的效果差异不大。在产生这些效果方面,NECA的效力约为R-PIA的十倍,效力顺序表明这些效果可能是由A2-腺苷受体的作用介导的。两种药物的效果均被咖啡因拮抗。单独给予咖啡因时会增加反应率。只有在单独使用时会降低反应率的R-PIA剂量下,R-PIA才会改变咖啡因产生的反应率增加。单独给药时无活性的NECA剂量会增强或减弱咖啡因的效果。这些结果不支持咖啡因产生的行为率增加(例如精神运动兴奋作用)是由于其对腺苷受体的拮抗作用这一观点。