Jones Jermaine D, Busse Gregory D, Riley Anthony L
Psychopharmacology Laboratory, Department of Psychology, American University, 4400 Massachusetts Ave., NW, Washington, DC 20016, USA.
Pharmacol Biochem Behav. 2006 Apr;83(4):554-60. doi: 10.1016/j.pbb.2006.03.017. Epub 2006 May 2.
Research using the conditioned taste aversion procedure has reported that a cocaine/alcohol combination induces a significantly stronger taste aversion than either cocaine or alcohol alone. These findings suggest that the co-administration of alcohol intensifies the aversive effects of cocaine. Although the behavioral interaction of cocaine and alcohol is well established, little is known about how the effects of this drug combination might be modulated by a variety of subject variables. The current investigation addressed this by assessing if the ability of alcohol to potentiate cocaine-induced taste aversions is dependent upon the strain and/or sex of the subject. In this series of studies, male and female rats of Long-Evans (Experiment 1) and Sprague-Dawley (Experiment 2) descent were given limited access to a novel saccharin solution to drink and were then injected with either vehicle, cocaine (20 mg/kg), alcohol (0.56 g/kg) or the alcohol/cocaine combination. This procedure was repeated every fourth day for a total of four conditioning trials. All subjects were then compared on an Aversion Test that followed the fourth conditioning cycle. In three of the groups tested (male Long-Evans; male and female Sprague-Dawley), cocaine induced a significant taste aversion that was unaffected by the co-administration of alcohol. However, in female Long-Evans subjects, the addition of alcohol significantly strengthened the avoidance of the saccharin solution. Although the effects of alcohol on cocaine-induced taste aversions are dependent upon an interaction of sex and strain, the basis for this SexxStrain interaction is not known. That such an interaction is evident suggests that attention to such factors in assessing the effects of drug combinations is important to understanding the likelihood of the use and abuse of such drugs.
使用条件性味觉厌恶程序进行的研究报告称,可卡因/酒精组合诱发的味觉厌恶比单独使用可卡因或酒精时显著更强。这些发现表明,酒精的共同给药会增强可卡因的厌恶效应。尽管可卡因和酒精的行为相互作用已得到充分证实,但对于这种药物组合的效果如何受到各种主体变量的调节却知之甚少。当前的研究通过评估酒精增强可卡因诱发味觉厌恶的能力是否取决于主体的品系和/或性别来解决这一问题。在这一系列研究中,给予长 Evans 品系(实验 1)和斯普拉格-道利品系(实验 2)的雄性和雌性大鼠有限机会饮用一种新型糖精溶液,然后分别注射赋形剂、可卡因(20 毫克/千克)、酒精(0.56 克/千克)或酒精/可卡因组合。此程序每四天重复一次,共进行四次条件性试验。然后在第四个条件性循环后的厌恶测试中对所有受试者进行比较。在测试的三组中(雄性长 Evans 品系;雄性和雌性斯普拉格-道利品系),可卡因诱发了显著的味觉厌恶,且不受酒精共同给药的影响。然而,在雌性长 Evans 品系受试者中,添加酒精显著增强了对糖精溶液的回避。尽管酒精对可卡因诱发味觉厌恶的影响取决于性别和品系的相互作用,但这种性别×品系相互作用的基础尚不清楚。这种相互作用的明显存在表明,在评估药物组合的效果时关注这些因素对于理解此类药物使用和滥用的可能性很重要。