Vol. 300, Issue 1, 157-161, January 2002

Relationship between Rate and Extent of G Protein Activation: Comparison between Full and Partial Opioid Agonists

John R. Traynor, Mary J. Clark and Ann E. Remmers

Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan

Opioid agonists acting at their receptors alter intracellular events by initiating activation of various types of Gi/Go proteins. This can be measured by the binding of the stable GTP analog [³⁵S]guanosine-5'-O-(3-thio)triphosphate ([³⁵S]GTPS). In this study agonist efficacy is defined by the degree to which an opioid stimulates the binding of [³⁵S]GTPS. This allows for a definition of full and partial agonists; a full agonist causing a greater stimulation of [³⁵S]GTPS binding than a partial agonist. The hypothesis that the rate of agonist-stimulated [³⁵S]GTPS binding is dependent upon agonist efficacy was tested using membranes from C6 glioma cells expressing µ- or -opioid receptors. At maximal concentrations the rate of agonist-stimulated [³⁵S]GTPS binding followed the efficacy of µ-agonists in stimulating [³⁵S]GTPS binding, i.e., [D-Ala²,N-Me-Phe⁴,Gly⁵-ol]-enkephalin > morphine > meperidine > butorphanol > nalbuphine. At submaximal concentrations of µ- or -full agonists the [³⁵S]GTPS association rate was also reduced, such that the rate of [³⁵S]GTPS binding correlated with the extent of [³⁵S]GTPS bound, whether this binding was stimulated by a full agonist or a partial agonist. Agonists also stimulated [³⁵S]GTPS dissociation, showing that binding of this stable nucleotide was reversible. Comparison of the -agonists [D-Ser²,Leu⁵]-enkephalin-Thr and (±)-4-((-R*)--((2S*,5R*)-4-allyl-2,5-dimethyl-1-piperazinyl)-3-hydroxylbenzyl)-N,N-diethylbenzamide, a compound with slow dissociation kinetics, showed the measured rate of G protein activation was not influenced by the agonist switching between receptors. The results are consistent with the idea that the active state(s) of the receptor induced by full or partial agonists is the same, but the number of activated receptors determines the rate of G protein activation.