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Exploring the first Rimonabant analog-​opioid peptide hybrid compound, as bivalent ligand for CB1 and opioid receptors

机译:探索第一个Rimonabant类似物-阿片肽杂化物,作为CB1和阿片受体的二价配体

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摘要

Cannabinoid (CB) and opioid systems are both involved in analgesia, food intake, mood and behavior. Due to the co-localization of µ-opioid (MOR) and CB1 receptors in various regions of the central nervous system (CNS) and their ability to form heterodimers, bivalent ligands targeting to both these systems may be good candidates to investigate the existence of possible cross-talking or synergistic effects, also at subeffective doses. In this work, we selected from a small series of new Rimonabant analogs one CB1R reverse agonist to be conjugated to the opioid fragment Tyr-D-Ala-Gly-Phe-NH2. The bivalent compound (9) has been used for in vitro binding assays, for in vivo antinociception models and in vitro hypothalamic perfusion test, to evaluate the neurotransmitters release.
机译:大麻素(CB)和阿片类药物系统均涉及镇痛,食物摄入,情绪和行为。由于在中枢神经系统(CNS)的各个区域中μ阿片类药物(MOR)和CB1受体共定位及其形成异二聚体的能力,因此针对这两个系统的二价配体可能是研究是否存在阿片类药物的良好候选者。在次有效剂量下也可能产生串扰或协同作用。在这项工作中,我们从一小部分新的Rimonabant类似物中选择一种CB1R反向激动剂与阿片样物质Tyr-D-Ala-Gly-Phe-NH2偶联。二价化合物(9)已用于体外结合测定,体内抗伤害感受模型和体外下丘脑灌注试验,以评估神经递质的释放。

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