Department of Psychiatry, Columbia University Medical Center, New York State Psychiatric Institute, New York, NY, USA.
Clinical Research and Development, Alkermes, Waltham, MA, USA.
Neuropsychopharmacology. 2017 Aug;42(9):1825-1832. doi: 10.1038/npp.2017.70. Epub 2017 Apr 10.
Ibudilast, a nonselective phosphodiesterase inhibitor, is used clinically in Asia for the treatment of asthma and poststroke dizziness. Recent preclinical studies have suggested that it also inhibits glial cell activation in rodents, and may alter opioid-mediated effects, including analgesia and withdrawal symptoms. The effects of ibudilast on the abuse potential of opioids in humans are largely unknown. The present study was designed to examine the influence of ibudilast on subjective (including drug craving), reinforcing, and analgesic effects of oxycodone in human volunteers diagnosed with opioid dependence (equivalent to moderate-severe opioid use disorder). Non-treatment-seeking opioid-dependent male volunteers (n=11) underwent an in-patient detoxification with morphine, followed by maintenance on placebo (0 mg b.i.d.) and active ibudilast (50 mg b.i.d.). Under each maintenance dose, six experimental sample and choice sessions were completed involving oral oxycodone administration (0, 15, and 30 mg/70 kg, p.o.). Subjective effects of oxycodone and drug craving were measured with visual analog scales (VAS) and a Drug Effects Questionnaire. The cold pressor test was used to produce pain, and a modified progressive-ratio choice procedure was used to measure the reinforcing effects of oxycodone. Under the active ibudilast condition compared with the placebo condition, ratings of drug liking following 15 mg of oxycodone were decreased significantly. The mean drug breakpoint value was also significantly lower in the active vs the placebo ibudilast condition under the 15 mg oxycodone condition, but not significantly lower under the 30 mg oxycodone condition. Heroin craving was significantly reduced under active ibudilast vs placebo, and similar effects were observed for tobacco and cocaine craving. Furthermore, mean subjective ratings of pain were lower in the active ibudilast condition. Our data suggest that ibudilast may be useful for treating opioid use disorders and it may enhance the analgesic effects of oxycodone.
伊布地尔是一种非选择性磷酸二酯酶抑制剂,在亚洲被临床用于治疗哮喘和中风后头晕。最近的临床前研究表明,它还可以抑制啮齿动物的神经胶质细胞激活,并且可能改变阿片类药物介导的作用,包括镇痛和戒断症状。伊布地尔对人类阿片类药物滥用潜力的影响在很大程度上尚不清楚。本研究旨在研究伊布地尔对诊断为阿片类药物依赖的人类志愿者(相当于中重度阿片类药物使用障碍)的氧可酮的主观(包括药物渴求)、强化和镇痛作用的影响。非治疗性寻求阿片类药物依赖的男性志愿者(n=11)接受了吗啡住院戒毒治疗,随后接受安慰剂(0mg b.i.d.)和活性伊布地尔(50mg b.i.d.)维持治疗。在每种维持剂量下,完成了六个实验样本和选择疗程,涉及口服氧可酮给药(0、15 和 30mg/70kg,po)。使用视觉模拟量表(VAS)和药物效应问卷测量氧可酮的主观效应和药物渴求。冷压试验用于产生疼痛,修改后的递增比例选择程序用于测量氧可酮的强化作用。与安慰剂条件相比,在活性伊布地尔条件下,15mg 氧可酮后的药物喜好评分显著降低。在 15mg 氧可酮条件下,活性伊布地尔与安慰剂伊布地尔条件下的平均药物断点值也显著降低,但在 30mg 氧可酮条件下则没有显著降低。在活性伊布地尔条件下,海洛因渴求显著降低,烟草和可卡因渴求也观察到类似的效果。此外,在活性伊布地尔条件下,平均主观疼痛评分较低。我们的数据表明,伊布地尔可能对治疗阿片类药物使用障碍有用,并且可能增强氧可酮的镇痛作用。