Department of Psychology, Western Michigan University, United States.
Pharmacol Biochem Behav. 2013 Sep;110:208-15. doi: 10.1016/j.pbb.2013.07.011. Epub 2013 Jul 21.
Modafinil is a novel wake-promoting drug with FDA approval for the treatment of sleep-related disorders that has recently been investigated as a potential agonist replacement therapy for psychostimulant dependence. Previous research in animals and humans indicates modafinil has a lower abuse liability than traditional psychostimulants, although few studies have carefully assessed modafinil's stimulus properties in combination with other psychostimulants. The current study trained male Sprague-Dawley rats to discriminate subcutaneous injections of 0.3 mg/kg (n=8) or 1.0 mg/kg d-amphetamine (n=8) from saline under an FR 20 schedule of food reinforcement and substitution tests were administered with d-amphetamine (0.03-1.0 mg/kg, s.c.), modafinil (32-256 mg/kg, i.g.), and a low modafinil dose (32 mg/kg, i.g.) in combination with d-amphetamine (0.03-1.0 mg/kg, s.c.) to determine if these drugs have additive effects. The selective D2 dopamine agonist, PNU-91356A, was also tested as a positive control and ethanol and morphine were tested as negative controls. Results indicate that modafinil produced dose-dependent and statistically significant d-amphetamine-lever responding in both groups and nearly complete substitution in animals trained to discriminate 1.0 mg/kg d-amphetamine. Modafinil pretreatment slightly increased the discrimination of low d-amphetamine doses in animals trained to discriminate 0.3 mg/kg d-amphetamine. These results support previous findings that modafinil and d-amphetamine may have additive effects. In consideration of recent interests in modafinil as an agonist treatment for psychostimulant dependence, additional preclinical investigations utilizing other methodologies to examine modafinil in combination with other stimulants, such as behavioral sensitization paradigms or drug self-administration, may be of interest.
莫达非尼是一种新型的促醒药物,已获得美国食品和药物管理局批准用于治疗与睡眠相关的疾病,最近已被研究作为潜在的兴奋剂依赖替代治疗药物。先前在动物和人类中的研究表明,莫达非尼的滥用倾向低于传统的兴奋剂,尽管很少有研究仔细评估莫达非尼与其他兴奋剂联合使用时的刺激特性。本研究训练雄性 Sprague-Dawley 大鼠辨别皮下注射 0.3mg/kg(n=8)或 1.0mg/kg 安非他命(n=8)与生理盐水,在 FR 20 食物强化时间表下进行训练,并进行替代测试,用安非他命(0.03-1.0mg/kg,皮下注射)、莫达非尼(32-256mg/kg,口服)和低剂量莫达非尼(32mg/kg,口服)与安非他命(0.03-1.0mg/kg,皮下注射)联合使用,以确定这些药物是否具有相加作用。选择性 D2 多巴胺激动剂 PNU-91356A 也作为阳性对照进行了测试,乙醇和吗啡作为阴性对照进行了测试。结果表明,莫达非尼在两组动物中均产生了剂量依赖性和统计学上显著的安非他命杠杆反应,并且在训练辨别 1.0mg/kg 安非他命的动物中几乎完全替代。莫达非尼预处理轻度增加了训练辨别 0.3mg/kg 安非他命的动物对低剂量安非他命的辨别。这些结果支持先前的发现,即莫达非尼和安非他命可能具有相加作用。考虑到最近对莫达非尼作为兴奋剂依赖的激动剂治疗的兴趣,利用其他方法学对莫达非尼与其他兴奋剂联合使用进行进一步的临床前研究,例如行为敏感化范式或药物自我给药,可能会很有趣。