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Ibudilast (AV-411):a new class therapeutic candidate for neuropathic pain and opioid withdrawal syndromes

机译:Ibudilast(AV-411):治疗神经性疼痛和阿片类药物戒断综合征的新型疗法

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The treatment of neuropathic pain is a major unresolved medical challenge.Present pharmacotherapies only have modest efficacy and numerous side effects.The use of opioid analgesics is additionally coupled with dependence and withdrawal syndromes.Ibudilast (AV-411) is a non-selective phosphodiesterase inhibitor that is also known to suppress glial cell activation.It has been used clinically for other indications with a good safety profile.As glial cell activation is considered to crucially contribute to neuropathic pain as well as opioid dependence and withdrawal,the authors conceived that ibudilast may be useful for treating these conditions.Preclinical data indicate that ibudilast crosses the blood-brain barrier,is well tolerated,is active on oral administration,reduces glial activation and attenuates pain symptoms in diverse rat models of neuropathic pain.In addition,it enhances acute morphine analgesia and attenuates morphine tolerance and withdrawal.Thus ibudilast may improve opioid efficacy and is a promising therapeutic candidate for neuropathic pain,with a novel mechanism of action.
机译:神经性疼痛的治疗是尚未解决的主要医学难题,目前的药物治疗仅具有中等疗效和许多副作用,使用阿片类镇痛药还伴有依赖性和戒断综合症。依布地司特(AV-411)是一种非选择性磷酸二酯酶抑制剂在临床上,它已被用于具有良好安全性的其他适应症。由于神经胶质细胞的激活被认为对神经性疼痛以及阿片样物质的依赖和戒断起关键作用,因此作者认为异丁司特可以临床数据表明,依布地司特可以跨越血脑屏障,具有良好的耐受性,口服活性强,减少神经胶质激活并减轻各种神经性疼痛大鼠模型的疼痛症状。此外,它可以增强急性吗啡镇痛并减弱吗啡耐受性和戒断能力d疗效好,是一种具有新型作用机制的神经性疼痛的有希望的治疗候选药物。

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