Macenski M J, Schaal D W, Cleary J, Thompson T
MSI-Substance Abuse Research Center, University of Texas-Houston Health Science Center 77030-3497.
Pharmacol Biochem Behav. 1994 Feb;47(2):379-83. doi: 10.1016/0091-3057(94)90027-2.
Seven rats lever pressed under a progressive ratio 3 (PR 3) schedule of food presentation; the number of responses per reinforcer systematically increased during each session. Break point (i.e., the number of responses in the last completed ratio before session termination) was measured under daily methadone (4.5 mg/kg and 3.0 mg/kg) or buprenorphine (0.3 mg/kg) administered prior to experimental sessions. Both drugs initially eliminated rats' food-maintained progressive-ratio responding. Break points during chronic methadone did not return to baseline levels after 80 drug sessions and a dose reduction. In contrast, break points during chronic buprenorphine administration were considerably above baseline control levels for two rats and returned to baseline levels for the third.
七只大鼠在逐步递增比率3(PR 3)的食物呈现时间表下按压杠杆;每次实验过程中,每个强化物的反应次数都系统地增加。在实验前每日给予美沙酮(4.5毫克/千克和3.0毫克/千克)或丁丙诺啡(0.3毫克/千克)的情况下,测量断点(即会话终止前最后完成比率中的反应次数)。两种药物最初都消除了大鼠由食物维持的逐步递增比率反应。在80次药物实验和剂量减少后,慢性美沙酮治疗期间的断点未恢复到基线水平。相比之下,在慢性丁丙诺啡给药期间,两只大鼠的断点显著高于基线对照水平,第三只大鼠的断点恢复到基线水平。