Rudski J M, Thomas D, Billington C J, Levine A S
Research and Medicine Service, Veterans Administration Medical Center, Minneapolis, MN 55417, USA.
Pharmacol Biochem Behav. 1995 Feb;50(2):271-6. doi: 10.1016/0091-3057(94)00313-8.
Opiate administration increases short-term free feeding in satiated rats. The feeding effects of the mixed opioid receptor agonist/antagonist buprenorphine were examined in both free-feeding and operant chamber paradigms. Buprenorphine (0.1 and 0.3 mg/kg) produced significant increases in short-term free feeding (i.e., 4 h), an effect enhanced by repeated administration. Buprenorphine's effects on operant responding were examined in satiated rats using a fixed ratio (FR) 80 (initial pellet) FR 3 (subsequent pellets) reinforcement schedule. Buprenorphine (0.03-0.3 mg/kg) decreased latency to begin responding for food, and increased total number of pellets consumed in a 1-h session. Increases in food intake relative to control were caused by continued responding for food as sessions progressed. Naloxone suppressed both the free-feeding and operant-contingent intake induced by buprenorphine. Thus, buprenorphine increases both freely available and lever-press contingent food intake.
给予阿片类药物可增加饱足大鼠的短期自由进食量。在自由进食和操作性条件反射箱范式中,研究了混合阿片受体激动剂/拮抗剂丁丙诺啡的进食效应。丁丙诺啡(0.1和0.3毫克/千克)显著增加了短期自由进食量(即4小时),重复给药可增强此效应。在饱足大鼠中,使用固定比率(FR)80(初始食丸)FR 3(后续食丸)强化程序研究了丁丙诺啡对操作性反应的影响。丁丙诺啡(0.03 - 0.3毫克/千克)缩短了开始为食物做出反应的潜伏期,并增加了1小时实验期间消耗的食丸总数。随着实验进程,相对于对照组,食物摄入量的增加是由于持续为食物做出反应所致。纳洛酮抑制了丁丙诺啡诱导的自由进食和操作性条件性进食。因此,丁丙诺啡增加了自由可得和通过按压杠杆获得的食物摄入量。