Comparative Pharmacological Effects of Lisuride and Lysergic Acid Diethylamide Revisited

Abstract

Lisuride is a non-psychedelic serotonin (5-HT) 2A receptor (5-HT 2A ) agonist and analogue of the psychedelic lysergic acid diethylamide (LSD). Lisuride also acts as an agonist at the serotonin 1A receptor (5-HT 1A ), a property known to counter psychedelic effects. Here, we tested whether lisuride lacks psychedelic activity due to a dual mechanism: (1) partial agonism at 5-HT 2A and (2) potent agonism at 5-HT 1A . The in vitro effects of lisuride, LSD, and related analogues on 5-HT 2A signaling were characterized by using miniGα q and β-arrestin 2 recruitment assays. The 5-HT 1A -and 5-HT 2A -mediated effects of lisuride and LSD were also compared in male C57BL/6J mice. The in vitro results confirmed that LSD is an agonist at 5-HT 2A , with high efficacy and potency for recruiting miniGα q and β-arrestin 2. By contrast, lisuride displayed partial efficacy for both functional end points (6−52% of 5-HT or LSD E max ) and antagonized the effects of LSD. The mouse experiments demonstrated that LSD induces head twitch responses (HTRs)(ED 50 = 0.039 mg/kg), while lisuride suppresses HTRs (ED 50 = 0.006 mg/kg). Lisuride also produced potent hypothermia and hypolocomotion (ED 50 = 0.008−0.023 mg/kg) that was blocked by the 5-HT 1A antagonist WAY100635 (3 mg/kg). Blockade of 5-HT 1A prior to lisuride restored basal HTRs, but it failed to increase HTRs above baseline levels. HTRs induced by LSD were blocked by lisuride (0.03 mg/kg) or the 5-HT 1A agonist 8-OH-DPAT (1 mg/kg). Overall, our findings show that lisuride is an ultrapotent 5-HT 1A agonist in C57BL/6J mice, limiting its use as a 5-HT 2A ligand in mouse studies examining acute drug effects. Results also indicate that the 5-HT 2A partial agonist-antagonist activity of lisuride explains its lack of psychedelic effects.