Effects of 5′-guanylylimidodiphosphate on the ligand binding of membrane-bound and solubilized opioid receptors of frog (Rana esculenta) brain

S. Benyhe, M. Szücs, E. Varga, A. Borsodi, M. Wollemann

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

The effect of the nonhydrolysable analogue of GTP, 5′-guanylylimidodiphosphate (GppNHp) was investigated on the binding of mu and kappa opioid agonists and antagonists in frog brain membrane preparations. The greatest inhibition with GppNHp was observed with labelled dihydromorphine, ([3H]DHM), a mu opioid receptor agonist. The binding of [3H]U-69593, a specific kappa opioid receptor agonist was inhibited to a smaller extent by GppNHp. Conversely, [3H]naloxone (opioid antagonist) binding displayed a dose-dependent increase with GppNHp, which effect was larger at 0°C than at 24°C. The binding of [3H]ethylketocyclazocine (EKC), a ligand with agonist-antagonist character was not affected by GppNHp either in the absence or in the presence of sodium ions at 0°C. Slight inhibition of [3H]EKC binding in the presence of sodium ions was observed with GppNHp at 24°C. In displacement experiments GppNHp decreased the ability of mu and kappa agonists to compete for [3H]naloxone binding sites. This effect was maintained after solubilization with 1% digitonin. However, since the binding of [3H]naloxone was also reduced, there was no agonist specificity of the GppNHp induced inhibition of binding to solubilized receptors. These results suggest that frog brain opioid receptors are coupled to a GTP-regulatory protein similar to mammalian opioid receptors.

Original languageEnglish
Pages (from-to)349-354
Number of pages6
JournalNeurochemistry international
Volume19
Issue number3
DOIs
Publication statusPublished - 1991

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Cell Biology

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