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 language | English (US) |
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Pages (from-to) | 116-121 |
Number of pages | 6 |
Journal | Journal of Pharmacology and Experimental Therapeutics |
Volume | 298 |
Issue number | 1 |
State | Published - 2001 |
Externally published | Yes |
ASJC Scopus subject areas
- Molecular Medicine
- Pharmacology