Characterization of [125I]AR-M100613, a high-affinity radioligand for delta opioid receptors

Peptides. 1999 Nov;20(11):1327-35. doi: 10.1016/s0196-9781(99)00138-2.

Abstract

AR-M100613 ([I]-Dmt-c[-D-Orn-2-Nal-D-Pro-D-Ala-]) is the iodinated analog of a cyclic casomorphin previously shown to be a potent antagonist at the delta opioid receptor. Specific [125I]AR-M100613 binding to rat whole brain membranes was saturable, reversible, and best fit to a one-site model (Kd = 0.080 +/- 0.008 nM, Bmax = 45.2 +/- 4.4 fmol/mg protein). [125I]AR-M100613 binding was displaced with high affinity by the delta opioid receptor ligands SNC-80, Deltorphin II and DPDPE but not the mu or kappa-selective receptor ligands DAMGO and U69593. Residual non-selective binding of [125I]AR-M 100613 to mu opioid receptors is blocked by the addition of CTOP to the assay buffer. [35S]GTPgammaS binding assays indicate that AR-M100613 is a potent, selective, and reversible antagonist for delta opioid receptors in rat brain membranes. The high-affinity, high specific activity, low nonspecific binding and antagonist profile of [125I]AR-M100613 favor its use as a radiochemical probe for delta opioid receptors.

MeSH terms

  • Animals
  • Brain / metabolism
  • Iodine Radioisotopes
  • Kinetics
  • Ligands
  • Male
  • Naltrexone / analogs & derivatives
  • Naltrexone / metabolism
  • Oligopeptides / metabolism
  • Radioligand Assay
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Opioid, delta / metabolism*

Substances

  • Iodine Radioisotopes
  • Ligands
  • Oligopeptides
  • Receptors, Opioid, delta
  • deltorphin II, Ala(2)-
  • Naltrexone
  • naltrindole