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RF9, a potent and selective neuropeptide FF receptor antagonist, prevents opioid-induced tolerance associated with hyperalgesia

机译:RF9是一种有效且选择性的神经肽FF受体拮抗剂,可预防阿片类药物引起的与痛觉过敏相关的耐受性

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Neuropeptide FF (NPFF) has been proposed to play a role in pain modulation, opioid tolerance, and several other physiological processes. However, pharmacological agents that would help define physiological roles for this peptide are still missing. Here we report the discovery of a potent and selective NPFF receptor antagonist, RF9, that can be administered systemically. This compound does not show any effects by itself but can block efficiently the increase in blood pressure and heart rate evoked by NPFF. When chronically coinjected with heroin, RF9 completely blocks the delayed and long-lasting paradoxical opioid-induced hyperalgesia and prevents the development of associated tolerance. Our data indicate that NPFF receptors are part of a bona fide antiopioid system and that selective antagonists of these receptors could represent useful therapeutic agents for improving the efficacy of opioids in chronic pain treatment.
机译:已经提出了神经肽FF(NPFF)在疼痛调节,阿片类药物耐受以及其他一些生理过程中发挥作用。但是,仍然缺少有助于确定该肽的生理作用的药理剂。在这里,我们报告发现可以全身给药的有效和选择性NPFF受体拮抗剂RF9。该化合物本身不显示任何作用,但可以有效地阻止NPFF引起的血压和心率升高。当与海洛因长期合用时,RF9完全阻断延迟和持久的自相矛盾的阿片类药物诱导的痛觉过敏,并阻止相关耐受性的发展。我们的数据表明,NPFF受体是真正的类阿片系统的一部分,这些受体的选择性拮抗剂可以代表有用的治疗剂,以改善阿片类药物在慢性疼痛治疗中的功效。

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