Winhusen T, Somoza E, Harrer J M, Moore E, Ussery T, Kropp F, Singal B, Elkashef A, Mojsiak J
Department of Psychiatry, University of Cincinnati College of Medicine, 3210 Jefferson Avenue, Cincinnati, OH 45220, USA.
Pharmacol Biochem Behav. 2005 Apr;80(4):631-8. doi: 10.1016/j.pbb.2005.01.017.
Pre-clinical research suggests that suppression of adrenocorticosteroid synthesis might decrease susceptibility to stress-induced relapse. Metyrapone effectively suppresses cortisol synthesis and thus might have promise as a cocaine dependence treatment. The present inpatient study evaluated the interaction of metyrapone and cocaine to assess the safety of conducting an outpatient trial. Twelve nontreatment-seeking cocaine-dependent individuals completed this double-blind, placebo-controlled, crossover study with two factors: medication (750 mg of metyrapone vs. placebo) and infusion (40 mg of cocaine vs. saline). Safety measures included vital signs, adverse events, and electrocardiogram. Efficacy measures included visual analog scale (VAS) ratings of craving and drug effect. Neuroendocrine measures included cortisol and ACTH. As predicted, metyrapone was well tolerated and did not exacerbate cocaine's physiological effects. Also as predicted, metyrapone did not significantly alter cocaine's subjective effects. The results of the present study suggest that metyrapone at the dose studied can likely be used safely in an outpatient study with active cocaine users.
临床前研究表明,抑制肾上腺皮质类固醇合成可能会降低应激诱导复发的易感性。美替拉酮可有效抑制皮质醇合成,因此有望成为治疗可卡因依赖的药物。本住院研究评估了美替拉酮与可卡因的相互作用,以评估开展门诊试验的安全性。12名未寻求治疗的可卡因依赖者完成了这项双盲、安慰剂对照、交叉研究,该研究有两个因素:药物(750毫克美替拉酮与安慰剂)和输注(40毫克可卡因与生理盐水)。安全指标包括生命体征、不良事件和心电图。疗效指标包括视觉模拟量表(VAS)对渴望和药物效果的评分。神经内分泌指标包括皮质醇和促肾上腺皮质激素(ACTH)。正如预期的那样,美替拉酮耐受性良好,不会加剧可卡因的生理效应。同样如预期的那样,美替拉酮不会显著改变可卡因的主观效应。本研究结果表明,在所研究的剂量下,美替拉酮可能可以安全地用于有活跃可卡因使用者的门诊研究。