coagonisten

Coagonisten, or coagonists, are ligands that bind to receptors in a way that supports or enables activation together with another ligand, often a primary agonist. In many receptor systems, full activation requires the simultaneous engagement of at least two binding events: one by the main agonist and another by a coagonist. The presence and concentration of a coagonist can thus tune the strength and probability of receptor opening without itself being the sole driver of activation.

The canonical example is the NMDA receptor, a ligand-gated ion channel in the brain. Glutamate, bound to the GluN2 site, serves as the primary agonist, while glycine or D-serine binds to a separate site on the GluN1 subunit. Both ligands must be occupied for efficient channel opening and calcium influx. Thus, glycine and D-serine act as endogenous coagonists that regulate synaptic plasticity and excitatory signaling. Coagonist occupancy can influence receptor responsiveness under physiological and pathological conditions, and regional variations in coagonist availability contribute to diverse signaling outcomes.

Coagonists are distinguished from other modulators in that they contribute directly to receptor activation when bound, often at distinct binding sites from the main agonist. However, not all receptors use coagonists; many rely on a single ligand for activation, while others employ allosteric modulators that alter affinity or efficacy without providing a separate activation event.

Clinical and pharmacological relevance centers on modulating coagonist levels or activity to influence NMDA receptor function. Strategies include inhibiting glycine transport to raise synaptic glycine or administering D-serine, with ongoing research into therapeutic benefits and safety considerations given the risk of excitotoxicity with excessive activation.