The beta adrenergic (beta) agonist salbutamol increased reinforcement
rates and decreased response rates on a differential-reinforcement-of-
low-rate (DRL) 72-S schedule. These changes in DRL 72-S schedule perfo
rmance are also produced by most clinically used antidepressants. The
effects of salbutamol on a DRL 72-S schedule were dose-dependently ant
agonized by the beta antagonist metoprolol, but not changed by the 5HT
antagonist methysergide. Additionally, neither salbutamol nor the ant
agonism of salbutamol by metoprolol caused disruption of DRL 72-S sche
dule performance. These results indicate that stimulation of beta rece
ptors, and not of 5HT receptors, mediates salbutamol antidepressant-li
ke effects on a DRL 72-S schedule.