Selective activation of Gαob by an adenosine A1 receptor agonist elicits analgesia without cardiorespiratory depression

Wall et al. describe the selective activation of an adenosine A1 receptor-mediated intracellular pathway that provides potent analgesia in the absence of sedation or cardiorespiratory depression, paving the way for novel medicines based on the far-reaching concept of selective G alpha agonism. The development of therapeutic agonists for G protein-coupled receptors (GPCRs) is hampered by the propensity of GPCRs to couple to multiple intracellular signalling pathways. This promiscuous coupling leads to numerous downstream cellular effects, some of which are therapeutically undesirable. This is especially the case for adenosine A(1) receptors (A(1)Rs) whose clinical potential is undermined by the sedation and cardiorespiratory depression caused by conventional agonists. We have discovered that the A(1)R-selective agonist, benzyloxy-cyclopentyladenosine (BnOCPA), is a potent and powerful analgesic but does not cause sedation, bradycardia, hypotension or respiratory depression. This unprecedented discrimination between native A(1)Rs arises from BnOCPA's unique and exquisitely selective activation of Gob among the six G alpha i/o subtypes, and in the absence of beta-arrestin recruitment. BnOCPA thus demonstrates a highly-specific G alpha-selective activation of the native A(1)R, sheds new light on GPCR signalling, and reveals new possibilities for the development of novel therapeutics based on the far-reaching concept of selective G alpha agonism.

Automated summary

The study discusses a method of selectively activating an intracellular pathway mediated by the adenosine A1 receptor, which provides potent analgesia without sedation or cardiorespiratory depression. This research opens up possibilities for the development of novel medicines based on selective G alpha agonism.