The G-protein-biased agents PZM21 and TRV130 are partial agonists of μ-opioid receptor-mediated signalling to ion channels

被引:34
作者
Yudin, Yevgen [1 ]
Rohacs, Tibor [1 ]
机构
[1] Rutgers New Jersey Med Sch, Dept Pharmacol Physiol & Neurosci, Newark, NJ 07103 USA
关键词
CONCISE GUIDE; PHARMACOLOGY; LIGAND; TRPM3; TRPV1; ACTIVATION;
D O I
10.1111/bph.14702
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and Purpose Opioids remain the most efficient medications against severe pain; they act on receptors that couple to heterotrimeric G-proteins in the G(alpha i/o) family. Opioids exert many of their acute effects through modulating ion channels via G(beta gamma) subunits. Many of their side effects are attributed to beta-arrestin recruitment. Several biased agonists that do not recruit beta-arrestins, but activate G-protein-dependent pathways, have recently been developed. While these compounds have been proposed to be full agonists of G-protein signalling in several high throughput pharmacological assays, their effects were not studied on ion channel targets. Experimental Approach Here, we used patch-clamp electrophysiology and Ca2+ imaging to test the effects of TRV130, PZM21, and herkinorin, three G-protein-biased agonists of mu-opioid receptors, on ion channel targets of G(alpha i/o)/G(beta gamma) signalling. We also studied G-protein dissociation using a FRET-based assay. Key Results All three biased agonists induced smaller activation of G-protein-coupled inwardly rectifying K+ channels (K(ir)3.2) and smaller inhibition of transient receptor potential melastatin (TRPM3) channels than the full mu receptor agonist DAMGO. Co-application of TRV130 or PZM21, but not herkinorin, alleviated the effects of DAMGO on both channels. PZM21 and TRV130 also decreased the effect of morphine on K(ir)3.2 channels. The Ca(V)2.2 channel was also inhibited less by PZM21 and TRV130 than by DAMGO. We also found that TRV130, PZM21, and herkinorin were less effective than DAMGO at inducing dissociation of the G(alpha i)/G(beta gamma) complex. Conclusion and Implications TRV130, PZM21, and potentially herkinorin are partial agonists of mu receptors.
引用
收藏
页码:3110 / 3125
页数:16
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