Tallarida Christopher S, Bires Kristopher, Avershal Jacob, Tallarida Ronald J, Seo Stephanie, Rawls Scott M
Department of Pharmacology, Temple University School of Medicine, Philadelphia, PA, USA; Center for Substance Abuse Research, Temple University, Philadelphia, PA, USA.
Department of Pharmacology, Temple University School of Medicine, Philadelphia, PA, USA; Center for Substance Abuse Research, Temple University, Philadelphia, PA, USA.
Alcohol. 2014 Sep;48(6):579-86. doi: 10.1016/j.alcohol.2014.07.006. Epub 2014 Aug 7.
More than 90% of individuals who use cocaine also report concurrent ethanol use, but only a few studies, all conducted with vertebrates, have investigated pharmacodynamic interactions between ethanol and cocaine. Planaria, a type of flatworm often considered to have the simplest 'brain,' is an invertebrate species especially amenable to the quantification of drug-induced behavioral responses and identification of conserved responses. Here, we investigated stereotypical and environmental place conditioning (EPC) effects of ethanol administered alone and in combination with cocaine. Planarians displayed concentration-related increases in C-shaped movements following exposure to ethanol (0.01-1%) (maximal effect: 9.9±1.1 C-shapes/5 min at 0.5%) or cocaine (0.1-5 mM) (maximal effect: 42.8±4.1 C-shapes/5 min at 5 mM). For combined administration, cocaine (0.1-5 mM) was tested with submaximal ethanol concentrations (0.01, 0.1%); the observed effect for the combination was enhanced compared to its predicted effect, indicating synergism for the interaction. The synergy with ethanol was specific for cocaine, as related experiments revealed that combinations of ethanol and nicotine did not result in synergy. For EPC experiments, ethanol (0.0001-1%) concentration-dependently increased EPC, with significant environmental shifts detected at 0.01 and 1%. Cocaine (0.001-1 μM) produced an inverted U-shaped concentration-effect curve, with a significant environmental shift observed at 0.01 μM. For combined exposure, variable cocaine concentrations (0.001-1 μM) were administered with a statistically ineffective concentration of ethanol (0.0001%). For each concentration of cocaine, the environmental shift was enhanced by ethanol, with significance detected at 1 μM. Cocaethylene, a metabolite of cocaine and ethanol, also produced C-shapes and EPC. Lidocaine (0.001-10 μM), an anesthetic and analog of cocaine, did not produce EPC or C-shaped movements. Evidence from planarians that ethanol produces place-conditioning effects and motor dysfunction, and interacts synergistically with cocaine, suggests that aspects of ethanol neuropharmacology are conserved across species.
超过90%使用可卡因的人也报告同时使用乙醇,但只有少数研究(均以脊椎动物为对象)调查了乙醇与可卡因之间的药效学相互作用。涡虫是一种常被认为具有最简单“大脑”的扁虫,是一种特别适合对药物诱导的行为反应进行量化以及识别保守反应的无脊椎动物物种。在此,我们研究了单独给予乙醇以及乙醇与可卡因联合使用时的刻板行为和环境位置条件反射(EPC)效应。涡虫在暴露于乙醇(0.01 - 1%)(最大效应:在0.5%时为9.9±1.1个C形/5分钟)或可卡因(0.1 - 5 mM)(最大效应:在5 mM时为42.8±4.1个C形/5分钟)后,C形运动呈现出浓度相关的增加。对于联合给药,可卡因(0.1 - 5 mM)与亚最大乙醇浓度(0.01、0.1%)一起进行测试;观察到的联合效应比其预测效应增强,表明存在相互作用的协同作用。与乙醇的协同作用对可卡因具有特异性,因为相关实验表明乙醇和尼古丁的组合不会产生协同作用。对于EPC实验,乙醇(0.0001 - 1%)浓度依赖性地增加EPC,在0.01%和1%时检测到显著的环境位置偏移。可卡因(0.001 - 1 μM)产生倒U形浓度效应曲线,在0.01 μM时观察到显著的环境位置偏移。对于联合暴露,可变浓度的可卡因(0.001 - 1 μM)与统计学上无效浓度的乙醇(0.0001%)一起给药。对于每种浓度的可卡因,乙醇增强了环境位置偏移,在1 μM时检测到显著性。可卡因和乙醇的代谢产物可口乙碱也产生C形运动和EPC。利多卡因(0.001 - 10 μM),一种可卡因的麻醉剂类似物,不会产生EPC或C形运动。来自涡虫的证据表明乙醇产生位置条件反射效应和运动功能障碍,并与可卡因协同相互作用,这表明乙醇神经药理学的某些方面在物种间是保守的。