Stimulation of guanosine-5′-O-(3-[35S]thio)triphosphate binding in digitonin-permeabilized C6 rat glioma cells: Evidence for an organized association of μ-opioid receptors and G protein

Andrew Alt, Iain J. Mcfadyen, Charles D. Fan, James H. Woods, John R. Traynor

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

The guanosine-5′-O-(3-[35S]thio)triphosphate ([35S]GTPγS) binding assay for the determination of relative opioid efficacy has been adapted to measure G protein activation in digitonin-permeabilized C6 rat glioma cells expressing a cloned μ-opioid receptor. The μ-agonist [D-Ala2,N-Me-Phe4,Gly5-ol]-enkephalin (DAMGO) caused a 3-fold increase in [35S]GTPγS binding over basal in a naloxone-sensitive manner. Relative μ-agonist efficacy was DAMGO > fentanyl ≥ morphine > buprenorphine. Nalbuphine showed no efficacy. G protein activation by receptors has been predicted to occur by random encounter. In this model a reduction in the number of receptors will decrease the rate of G protein activation but not the maximum number of G proteins activated. To test this [model C6 μ cells were treated with the irreversible μ-antagonist β-funaltrexamine (10 nM) prior to permeabilization. This reduced the number of μ-opioid receptors determined with [3H]diprenorphine to 23 ± 3% of control with no change in affinity. A commensurate reduction (to 29 ± 10% of control) in the level of [35S]GTPγS binding stimulated by DAMGO was observed, but the t1/2 for [35S]GTPγS binding remained unchanged. Thus, random encounters of receptor and G protein failed to occur in this permeabilized cell preparation. A model that assumes an organized association of G proteins with receptors better describes the activation of G proteins by opioid μ-receptors.

Original languageEnglish (US)
Pages (from-to)116-121
Number of pages6
JournalJournal of Pharmacology and Experimental Therapeutics
Volume298
Issue number1
StatePublished - 2001
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology

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