Supraspinal and spinal effects of [Phe1Ψ(CH2-NH)Gly2]-nociceptin(1–13)-NH2 on nociception in the rat

This publication has 31 references indexed in Scilit:

• ORL1, a novel member of the opioid receptor family
  Published by Wiley ,2001
• Evidence that [Phe¹ψ(CH₂‐NH)Gly²]nociceptin‐(1‐13)‐NH₂, a peripheral ORL‐1 receptor antagonist, acts as an agonist in the rat spinal cord
  British Journal of Pharmacology, 1998
• Pharmacological characterization of the nociceptin receptor mediating hyperalgesia in the mouse tail withdrawal assay
  British Journal of Pharmacology, 1998
• [Phe1Ψ(CH2-NH)Gly2]-nociceptin-(1-13)NH2, a proposed antagonist of the nociceptin receptor, is a potent and stable agonist in the rat spinal cord
  Neuroscience Letters, 1998
• Bidirectional modulatory effect of orphanin FQ on morphine‐induced analgesia: antagonism in brain and potentiation in spinal cord of the rat
  British Journal of Pharmacology, 1997
• Biochemical Evidence for Orphanin FQ/Nociceptin Receptor Heterogeneity in Mouse Brain
  Biochemical and Biophysical Research Communications, 1997
• Orphanin FQ: A Neuropeptide That Activates an Opioidlike G Protein-Coupled Receptor
  Science, 1995
• Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor
  Nature, 1995
• cDNA Cloning of an orphan opiate receptor gene family member and its splice variant
  FEBS Letters, 1994
• Ethical guidelines for investigations of experimental pain in conscious animals
  PAIN®, 1983