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Discovery of dual-acting opioid ligand and TRPV1 antagonists as novel therapeutic agents for pain

机译:将双作用性配体和TRPV1拮抗剂的发现作为疼痛的新疗递

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In order to discover a novel type of analgesic, we investigated dual activity ligands with TRPV1 antagonism and mu-opioid receptor affinity with the goal of eliciting synergistic analgesia while avoiding the side effects associated with single targeting. Based on a combination approach, a series of 4-benzyl-4-(dimethylamino)piperidinyl analogues were designed, synthesized and evaluated for their receptor activities. Among them, compound 49 exhibited the most promising dual-acting activity toward TRPV1 and the mu-opioid receptor in vitro. In vivo, 49 displayed potent, dose-dependent antinociceptive activity in both the 1st and 2nd phases in the formalin assay. Consistent with its postulated mechanism, we confirmed that in vivo, as in vitro, compound 49 both antagonized TRPV1 and functioned as a mu-opioid agonist. This result indicates that dual-acting TRPV1 antagonist/mu-opioid ligands can be made and represent a new and promising class of analgesic. (C) 2019 Elsevier Masson SAS. All rights reserved.
机译:为了发现一种新型镇痛,我们研究了具有Trpv1拮抗作用的双活性配体和u-Fapioid受体亲和力,其目的是引发协同镇痛,同时避免与单一靶向相关的副作用。基于组合方法,设计了一系列4-苄基-4-(二甲基氨基)哌啶基类似物,用于其受体活性。其中,化合物49表现出对TRPV1和体外MU-阿片受体的最有前途的双作用活性。在福尔马林测定中的第1和第2阶段,49体内显示出有效的剂量依赖性抗肌肉活性活性。与其假设机制一致,我们证实在体内,如体外,化合物49都拮抗的TRPV1并用作Mu-阿片类激动剂。该结果表明,可以制备双作用Trpv1拮抗剂/ u-Fomioid配体并代表新的和有前途的镇痛类。 (c)2019年Elsevier Masson SAS。版权所有。

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