Opioid receptor binding and in vivo antinociceptive activity of position 3-substituted morphiceptin analogs

Biochem Biophys Res Commun. 2004 Jul 23;320(2):531-6. doi: 10.1016/j.bbrc.2004.05.202.

Abstract

Analogs of morphiceptin (Tyr-Pro-Phe-Pro-NH2), a mu-selective opioid receptor ligand, with position 3-modifications, including altered size, lipophilicity, and electronic character, while maintaining aromaticity were synthesized. The activity of the new analogs in in vitro assays and in in vivo hot-plate test of analgesia was compared and the results were consistent. [D-1-Nal3]Morphiceptin was the most potent analog of this series with a 26-fold increase in mu-opioid receptor affinity, a 15-fold potency increase in the GPI assay, and a significant potency increase in the hot-plate analgesic test, as compared with morphiceptin. [d-Qal3]Morphiceptin was found to be a weak antagonist in the GPI assay.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Analgesics, Opioid / metabolism*
  • Analgesics, Opioid / pharmacology
  • Animals
  • Endorphins / chemistry
  • Endorphins / metabolism*
  • Endorphins / pharmacology
  • Mice
  • Protein Binding
  • Rats
  • Rats, Wistar
  • Receptors, Opioid / metabolism*
  • Structure-Activity Relationship

Substances

  • Analgesics, Opioid
  • Endorphins
  • Receptors, Opioid
  • morphiceptin