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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Combined effects of modafinil and d-amphetamine in male Sprague-Dawley rats trained to discriminate d-amphetamine
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Combined effects of modafinil and d-amphetamine in male Sprague-Dawley rats trained to discriminate d-amphetamine

机译:莫达非尼和d-苯异丙胺对训练以区分d-苯异丙胺的雄性Sprague-Dawley大鼠的联合作用

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摘要

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 damphetamine. 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 selfadministration, may be of interest.
机译:莫达非尼(Modafinil)是经FDA批准用于治疗与睡眠有关的疾病的新型促唤醒药物,最近已被研究用作精神兴奋药依赖性的潜在激动剂替代疗法。先前在动物和人类中的研究表明,莫达非尼的滥用责任要比传统的精神兴奋剂低,尽管很少有研究结合其他精神兴奋剂来仔细评估莫达非尼的刺激特性。当前的研究训练了雄性Sprague-Dawley大鼠,根据FR 20食品强化和替代试验,区分了从盐水中皮下注射0.3 mg / kg(n = 8)或1.0 mg / kg d-苯异丙胺(n = 8)。 d-苯丙胺(0.03-1.0 mg / kg,sc),莫达非尼(32-256 mg / kg,ig)和低莫达非尼剂量(32 mg / kg,ig)与d-苯丙胺(0.03- 1.0 mg / kg,sc)以确定这些药物是否具有累加作用。还测试了选择性D2多巴胺激动剂PNU-91356A作为阳性对照,并测试了乙醇和吗啡作为阴性对照。结果表明,莫达非尼在两组中均产生剂量依赖性和统计学上显着的d-苯丙胺杠杆反应,并且在受过训练以区别于1.0 mg / kg甲基苯丙胺的动物中几乎完全替代。莫达非尼预处理可稍微提高对经训练可区分0.3 mg / kg d-苯异丙胺的动物对低d-苯异丙胺剂量的区分。这些结果支持以前的发现,莫达非尼和d-苯异丙胺可能具有累加作用。考虑到最近对莫达非尼作为精神刺激药依赖性激动剂治疗的兴趣,可能需要进行其他临床前研究,利用其他方法结合其他兴奋剂(如行为敏化范例或药物自我给药)来检查莫达非尼。

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