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

Frédéric Simonin(Institut de Biochimie et Génétique Cellulaires), Martine Schmitt(Institut de Biochimie et Génétique Cellulaires), Jean‐Paul Laulin(Institut de Biochimie et Génétique Cellulaires), Emilie Laboureyras(Institut de Biochimie et Génétique Cellulaires), Jack H. Jhamandas(Institut de Biochimie et Génétique Cellulaires), David MacTavish(Institut de Biochimie et Génétique Cellulaires), Audrey Matifas(Institut de Biochimie et Génétique Cellulaires), Catherine Mollereau(Institut de Biochimie et Génétique Cellulaires), Patrick Laurent(Institut de Biochimie et Génétique Cellulaires), Marc Parmentier(Institut de Biochimie et Génétique Cellulaires), Brigitte L. Kieffer(Institut de Biochimie et Génétique Cellulaires), Jean‐Jacques Bourguignon(Institut de Biochimie et Génétique Cellulaires), Guy Simonnet(Institut de Biochimie et Génétique Cellulaires)
Proceedings of the National Academy of Sciences
January 3, 2006
Cited by 224Open Access
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Abstract

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.


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