Leander J D
Pharmacol Biochem Behav. 1978 Aug;9(2):191-4. doi: 10.1016/0091-3057(78)90163-6.
The effects of normeperidine (1-17.5 mg/kg) alone and in the presence of naloxone (1 and 10 mg/kg) were studied in pigeons responding under a multiple fixed-ratio 30 response, fixed-interval 5-min schedule of food presentation. Naloxone only potentiated the rate-decreasing effects of normeperidine. The effects of meperidine also were studied after pretreatment with SKF-525A (25 and 50 mg/kg), an inhibitor of drug metabolism. SKF-525A had no effects on responding when administered alone, but it potentiated the rate-decreasing effects of meperidine. It was concluded that meperidine's rate-decreasing effects cannot be due to normeperidine, the metabolite, but rather that both of these drugs have non-narcotic actions which produce decreases in schedule-controlled responding.
在鸽子按照多重固定比率30次反应、固定间隔5分钟的食物呈现时间表做出反应的情况下,研究了单独使用去甲哌替啶(1 - 17.5毫克/千克)以及在纳洛酮(1和10毫克/千克)存在时的效果。纳洛酮仅增强了去甲哌替啶的降低反应率的作用。在用药物代谢抑制剂SKF - 525A(25和50毫克/千克)预处理后,也研究了哌替啶的效果。单独给予SKF - 525A时对反应没有影响,但它增强了哌替啶的降低反应率的作用。得出的结论是,哌替啶的降低反应率作用并非由于其代谢产物去甲哌替啶,而是这两种药物都具有非麻醉作用,从而导致按时间表控制的反应减少。