Endogenous mammalian RF-amide peptides, including PrRP, kisspeptin and 26RFa, modulate nociception and morphine analgesia via NPFF receptors.

@article{Elhabazi2013EndogenousMR,
  title={Endogenous mammalian RF-amide peptides, including PrRP, kisspeptin and 26RFa, modulate nociception and morphine analgesia via NPFF receptors.},
  author={Khadija Elhabazi and J A Humbert and Isabelle Bertin and Martine Schmitt and Fr{\'e}d{\'e}ric Bihel and Jean-Jacques Bourguignon and Bernard Bucher and J{\'e}r{\^o}me A J Becker and Tania Sorg and Hamid Meziane and B Petit-demouli{\`e}re and Brigitte Ilien and Fr{\'e}d{\'e}ric Simonin},
  journal={Neuropharmacology},
  year={2013},
  volume={75},
  pages={164-71}
}
Mammalian RF-amide peptides are encoded by five different genes and act through five different G protein-coupled receptors. RF-amide-related peptides-1 and -3, neuropeptides AF and FF, Prolactin releasing peptides, Kisspeptins and RFa peptides are currently considered endogenous peptides for NPFF1, NPFF2, GPR10, GPR54 and GPR103 receptors, respectively. However, several studies suggest that the selectivity of these peptides for their receptors is low and indicate that expression patterns for… CONTINUE READING
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