Parrilla-Carrero Jeffrey, Figueroa Orialis, Lugo Alejandro, García-Sosa Rebecca, Brito-Vargas Paul, Cruz Beatriz, Rivera Mélanis, Barreto-Estrada Jennifer L
Department of Science and Technology, AGMUS, Universidad del Este, Carolina, Puerto Rico.
Drug Alcohol Depend. 2009 Feb 1;100(1-2):122-7. doi: 10.1016/j.drugalcdep.2008.09.014. Epub 2008 Nov 22.
Anabolic androgenic steroids (AAS) are often misused by adolescents and athletes. Their effects vary according to chemical structure and metabolism, route of administration, and AAS regimen. In this study, adult C57Bl/6 male mice were systemically exposed to testosterone propionate (TP), nandrolone or 17alpha-methyltestosterone (17alpha-meT), type I, type II and type III AAS, respectively, in order to determine the hedonic or aversive properties of each drug. For this purpose, the conditioned place preference (CPP) test was employed at three different AAS doses (0.075, 0.75 and 7.5 mg/kg). Other behavioral domains monitored were light-dark transitions (side changes) and general activity. TP shifted place preference at all doses tested, and nandrolone shifted place preference at 0.75 and 7.5 mg/kg, but not at 0.075 mg/kg, the lower dose tested. Conversely, mice receiving 17alpha-meT did not show alteration in the preference score. The lower dose of nandrolone did modify exploratory-based anxiety showing a decrease in light-dark transitions if compared to vehicle-treated animals, while mice treated with TP or 17alpha-meT were not affected. Our data suggest that when studying hedonic and rewarding properties of synthetic androgens, distinction has to be made based on type of AAS and metabolism.
合成代谢雄激素类固醇(AAS)常被青少年和运动员滥用。其效果因化学结构、代谢、给药途径及AAS方案而异。在本研究中,成年C57Bl/6雄性小鼠分别被系统性给予丙酸睾酮(TP)、诺龙或17α-甲基睾酮(17α-meT),即I型、II型和III型AAS,以确定每种药物的享乐或厌恶特性。为此,在三种不同的AAS剂量(0.075、0.75和7.5 mg/kg)下采用条件性位置偏爱(CPP)试验。监测的其他行为领域为明暗转换(侧别改变)和一般活动。TP在所有测试剂量下均改变了位置偏爱,诺龙在0.75和7.5 mg/kg剂量下改变了位置偏爱,但在测试的较低剂量0.075 mg/kg下未改变。相反,接受17α-meT的小鼠偏爱得分未显示改变。与给予赋形剂处理的动物相比,较低剂量的诺龙确实改变了基于探索的焦虑,表现为明暗转换减少,而用TP或17α-meT处理的小鼠未受影响。我们的数据表明,在研究合成雄激素的享乐和奖赏特性时,必须根据AAS类型和代谢进行区分。