Varenicline Is a Potent Agonist of the Human 5-Hydroxytryptamine_3 Receptor

Abstract

Varenicline, a widely used and successful smoking cessation agent, acts as a partial agonist at nicotinic acetylcholine receptors. Here, we explore the effects of varenicline at human and mouse 5-Hydroxytryptamine_3 (5-HT_3) receptors. Application of varenicline to human 5-HT_3 receptors expressed in Xenopus laevis oocytes reveal it is almost a full agonist (R_max = 80%) with an EC_50 (5.9 μM) 3-fold higher than 5-HT. At mouse 5-HT_3 receptors varenicline is a partial agonist (R_max = 35%) with an EC50 (18 μM) 20-fold higher than 5-HT. Displacement of the competitive 5-HT_3 receptor antagonist [^(3)H]granisetron reveals similar IC_50 values for varenicline at mouse and human receptors expressed in human embryonic kidney 293 cells, although studies in these cells using a membrane potential-sensitive dye show that again varenicline is a 4- or 35-fold less potent agonist than 5-HT in human and mouse receptors, respectively. Thus the data suggest that the efficacy, but not the affinity, of varenicline is greater at human 5-HT3 receptors compared with mouse. Docking studies provide a possible explanation for this difference, because they suggest distinct orientations of the ligand in the mouse versus human 5-HT_3 agonist binding sites. Additional binding selectivity studies in a broad panel of recombinant receptors and enzymes confirmed an interaction with 5-HT_3 receptors but revealed no additional interactions of varenicline. Therefore, activation of human 5-HT_3 receptors may be responsible for some of the side effects that preclude use of higher doses during varenicline treatment.

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