Wei Huimei, Zhang Ting, Zhan Chang-Guo, Zheng Fang
Molecular Modeling and Biopharmaceutical Center, College of Pharmacy, University of Kentucky, 789 South Limestone Street, Lexington, KY, 40536, USA; Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 789 South Limestone Street, Lexington, KY, 40536, USA.
Molecular Modeling and Biopharmaceutical Center, College of Pharmacy, University of Kentucky, 789 South Limestone Street, Lexington, KY, 40536, USA; Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 789 South Limestone Street, Lexington, KY, 40536, USA.
Neuropharmacology. 2020 Aug 1;172:108128. doi: 10.1016/j.neuropharm.2020.108128. Epub 2020 May 8.
As a novel first-in-class potent analgesic acting as an agonist of multiple opioid receptors, cebranopadol showed high efficacy and good tolerability in a broad range of preclinical models and clinical trials related to pain. In the present study, to evaluate the efficacy and safety of cebranopadol as a potential treatment of cocaine dependence, we tested the effects of cebranopadol with single and repeated doses (25, 50, 75, or 100 μg/kg, oral gavage) using rat models of cocaine fixed-ratio (FR) self-administration (SA), cocaine progressive-ratio (PR) SA, and sucrose pellet SA. In single-dosing treatment paradigm, cebranopadol significantly and dose-dependently reduced cocaine SA under FR and PR schedules and suppressed food intake under FR schedule without causing apparent side effects. In repeated-dosing treatment scheme, i.e. daily administration of 25, 50, 75, or 100 μg/kg cebranopadol for a week, the similar reduction in cocaine intake was detected, while non-negligible complications/side effects were observed at repeated high doses (75 and 100 μg/kg). The observed side effects were similar to the common toxic signs elicited by heroin at high doses, although cebranopadol did not fully substitute heroin's discriminative stimulant effects in our drug discriminative tests. These results demonstrated that the most appropriate oral dose of cebranopadol to balance the efficacy and safety is 50 μg/kg. Collectively, although cebranopadol may serve as a new treatment for cocaine dependence, more consideration, cautiousness, and a clear optimal dose window to dissociate its therapeutic effects from opioid side effects/complications in male and female subjects will be necessary to increase its practical clinical utility.
作为一种新型的、一流的强效镇痛药,作为多种阿片受体的激动剂,cebranopadol在一系列与疼痛相关的临床前模型和临床试验中显示出高效性和良好的耐受性。在本研究中,为了评估cebranopadol作为可卡因依赖潜在治疗方法的疗效和安全性,我们使用可卡因固定比率(FR)自我给药(SA)、可卡因累进比率(PR)SA和蔗糖颗粒SA的大鼠模型,测试了单次和重复剂量(25、50、75或100μg/kg,口服灌胃)的cebranopadol的效果。在单次给药治疗范式中,cebranopadol在FR和PR给药方案下显著且剂量依赖性地减少了可卡因SA,并在FR给药方案下抑制了食物摄入,且未引起明显的副作用。在重复给药治疗方案中,即每天给予25、50、75或100μg/kg的cebranopadol,持续一周,检测到可卡因摄入量有类似的减少,而在重复高剂量(75和100μg/kg)时观察到了不可忽视的并发症/副作用。观察到的副作用与高剂量海洛因引起的常见毒性体征相似,尽管cebranopadol在我们的药物辨别试验中并未完全替代海洛因的辨别性刺激作用。这些结果表明,平衡疗效和安全性的cebranopadol最合适的口服剂量是50μg/kg。总体而言,尽管cebranopadol可能作为可卡因依赖的一种新治疗方法,但为了提高其实际临床效用,需要更多的考虑、谨慎以及明确的最佳剂量窗口,以区分其治疗效果与男性和女性受试者的阿片类副作用/并发症。