Panlilio Leigh V, Yasar Sevil, Nemeth-Coslett Ro, Katz Jonathan L, Henningfield Jack E, Solinas Marcello, Heishman Stephen J, Schindler Charles W, Goldberg Steven R
Preclinical Pharmacology Section, Intramural Research Program, National Institute on Drug Abuse, Baltimore, MD, USA.
Neuropsychopharmacology. 2005 Feb;30(2):433-43. doi: 10.1038/sj.npp.1300599.
Second-order schedules of drug self-administration were developed to incorporate the effects of drug-related environmental stimuli into an animal model of drug abuse, making it more similar to human situations. Ironically, little is known about how human subjects behave under these schedules. In this study, human volunteers with a history of cocaine use worked on a second-order schedule in which every 100th lever response produced an auditory-visual brief stimulus (2 s). The first stimulus produced after 1 h was extended to 10 s and paired with an intravenous injection of cocaine (25 mg). Up to three injections were allowed per session. In different phases of the experiment, presentation of the brief stimulus was discontinued and/or saline solution (placebo) was injected instead of cocaine. Injections of cocaine were found to maintain responding even when the brief stimulus was not presented. Placebo injections alone did not maintain responding. In contrast, the brief stimulus maintained high levels of responding under placebo conditions, even though self-reports indicated that subjects could clearly discriminate that they were not receiving cocaine. These results demonstrate that drug-related environmental stimuli can maintain persistent drug seeking during periods of drug unavailability. As this procedure directly measures the effects of stimuli on drug seeking, it may provide a valuable complement to indirect measures, such as self-reports of craving, that are often used with human subjects. The similarity of the response patterns in humans and animals also supports the use of second-order schedules in animals as a valid model of human drug seeking.
药物自我给药的二阶程序被开发出来,以便将与药物相关的环境刺激的影响纳入药物滥用的动物模型中,使其更类似于人类的情况。具有讽刺意味的是,对于人类受试者在这些程序下的行为知之甚少。在这项研究中,有可卡因使用史的人类志愿者按照二阶程序进行操作,其中每第100次杠杆反应会产生一个视听简短刺激(2秒)。1小时后产生的第一个刺激延长至10秒,并与静脉注射可卡因(25毫克)配对。每次实验允许最多注射三次。在实验的不同阶段,停止呈现简短刺激和/或注射生理盐水(安慰剂)而不是可卡因。结果发现,即使不呈现简短刺激,注射可卡因也能维持反应。仅注射安慰剂并不能维持反应。相比之下,即使自我报告表明受试者能够清楚地辨别他们没有接受可卡因,但在安慰剂条件下,简短刺激仍能维持较高水平的反应。这些结果表明,与药物相关的环境刺激可以在无法获得药物的期间维持持续的觅药行为。由于该程序直接测量刺激对觅药行为的影响,它可能为间接测量(如经常用于人类受试者的渴望自我报告)提供有价值的补充。人类和动物反应模式的相似性也支持在动物中使用二阶程序作为人类觅药行为的有效模型。