John William S, Nader Michael A
Department of Physiology and Pharmacology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1083, United States.
Department of Physiology and Pharmacology, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157-1083, United States.
Drug Alcohol Depend. 2017 Jan 1;170:112-119. doi: 10.1016/j.drugalcdep.2016.11.002. Epub 2016 Nov 10.
Concurrent alcohol use among cocaine abusers is common but the behavioral variables that promote co-abuse are not well understood. The present study examined the effects of intragastric (i.g.) ethanol (EtOH) administration in monkeys responding under a schedule of cocaine reinforcement in which extensive drug seeking was maintained by conditioned stimuli.
Four adult male cynomolgus monkeys (Macaca fascicularis) were trained to respond under a second-order fixed-interval (FI) 600s (fixed-ratio (FR) 30:S) schedule of cocaine (0.003-0.56mg/kg/injection) presentation. Sessions ended after 5 injections or 90min had elapsed. Different EtOH doses (0.5-2.0g/kg, i.g.) were administered 30min before the session, typically on Tuesdays and Fridays. Blood ethanol concentrations (BECs) were also assessed. Pattern of FI responding was assessed by determining quarter-life (QL) values.
Cocaine self-administration was characterized as an inverted U-shaped function of dose; QL values increased monotonically with dose. EtOH pretreatments dose-dependently decreased self-administration at several cocaine doses in 3 of 4 monkeys. In one animal, EtOH increased low-dose cocaine-maintained responding. For all monkeys, QL values were increased by EtOH when low- and high-cocaine doses were self-administered, suggesting additive effects of EtOH and cocaine. Furthermore, BECs were not altered following cocaine self-administration.
The reductions in cocaine self-administration and the increases in QL values following EtOH, suggest that EtOH was enhancing cocaine-related conditioned reinforcement. A better understanding of the behavioral mechanisms that mediate the co-abuse of alcohol and cocaine will lead to improved treatments for both drugs.
可卡因滥用者中同时使用酒精的情况很常见,但促进共同滥用的行为变量尚未得到很好的理解。本研究考察了胃内(i.g.)给予乙醇(EtOH)对猴子在可卡因强化程序下反应的影响,在该程序中,广泛的觅药行为由条件刺激维持。
对四只成年雄性食蟹猴(猕猴)进行训练,使其在二阶固定间隔(FI)600秒(固定比率(FR)30:1)的可卡因(0.003 - 0.56毫克/千克/注射)呈现程序下做出反应。在5次注射或90分钟过去后,实验结束。通常在周二和周五,在实验开始前30分钟给予不同剂量的EtOH(0.5 - 2.0克/千克,i.g.)。还评估了血液乙醇浓度(BECs)。通过确定四分之一寿命(QL)值来评估FI反应模式。
可卡因自我给药表现为剂量的倒U形函数;QL值随剂量单调增加。在4只猴子中的3只中,EtOH预处理在几个可卡因剂量下剂量依赖性地减少了自我给药。在一只动物中,EtOH增加了低剂量可卡因维持的反应。对于所有猴子,当自我给药低剂量和高剂量可卡因时,EtOH都会增加QL值,表明EtOH和可卡因具有相加作用。此外,可卡因自我给药后BECs没有改变。
EtOH后可卡因自我给药的减少和QL值的增加表明,EtOH增强了与可卡因相关的条件强化。更好地理解介导酒精和可卡因共同滥用的行为机制将导致对这两种药物的治疗得到改善。