Abstract

Crosstalk between opioid and adrenergic receptors is well characterized and due to interactions between second messenger systems, formation of receptor heterodimers, and extracellular allosteric binding regions. Both classes of receptors bind both sets of ligands. We propose here that receptor crosstalk may be mirrored in ligand complementarity. We demonstrate that opioids bind to adrenergic compounds with micromolar affinities. Additionally, adrenergic compounds bind with micromolar affinities to extracellular loops of opioid receptors while opioids bind to extracellular loops of adrenergic receptors. Thus, each compound type can bind to the complementary receptor, enhancing the activity of the other compound type through an allosteric mechanism. Screening for ligand complementarity may permit the identification of other mutually-enhancing sets of compounds as well as the design of novel combination drugs or tethered compounds with improved duration and specificity of action.

Highlights

  • Many receptor systems engage in crosstalk, modifying each other’s activity

  • Adrenergic compounds bind with micromolar affinities to extracellular loops of opioid receptors while opioids bind to extracellular loops of adrenergic receptors

  • Because opioids and adrenergic compounds modify each other’s physiological activities, these sets of compounds should be molecularly complementary and bind to each other according to our first proposition

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Summary

Introduction

Many receptor systems engage in crosstalk, modifying each other’s activity. Understanding how such crosstalk evolved and the molecular mechanisms that mediate receptor interactions would obviously be a boon to drug developers, especially if, in addition, it were possible to predict such interactions in advance and to take advantage of their unique properties. Adrenergic drugs ( epinephrine, clonidine, and amphetamines) enhance opioid receptor activity [40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55], again by means of an extracellular binding site [56]. In both cases, the enhancement is such that in the presence of the enhancer, the primary ligand attains full activity at significantly lower concentrations than when the ligand is alone. Adrenergic compounds have been demonstrated to bind to low affinity opioid binding sites on opioid receptors [56,64], while opioids bind to a site immediately adjacent to the high affinity binding site of adrenergic receptors [39,40,41,65,66]

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