Serotonin modulates optimized coding of natural stimuli through increased neural and behavioural responses via enhanced burst firing.

Understanding how the processing of sensory information leads to behavioural responses remains a central problem in systems neuroscience. Here, we investigated how the neuromodulator serotonin affects neural and behavioural responses to second-order envelope stimuli within the electrosensory system of the weakly electric fish Apteronotus leptorhynchus. We found that serotonin application increased neuronal excitability through greater tendency for burst firing. We found that increased excitability led to overall higher neural sensitivities to higher envelope frequencies. Separating the spike train into bursts and isolated spike train components revealed that this was due to significant increases in neural sensitivity for the former but not the latter. We next investigated the consequences of such changes in sensitivity towards optimized coding of stimuli with specific statistics. Our results show that serotonin application compromised optimal coding of stimuli with statistics seen under naturalistic conditions due to changes in burst, but not isolated spike firing. Finally, we found that serotonin application increased behavioural sensitivity to envelope stimuli. Interestingly, changes in neural sensitivity due to bursts were a far better predictor of changes in behavioural sensitivity, suggesting that burst firing is decoded by downstream brain areas. Overall, our results suggest that serotonin modulates neural responses to optimize coding and perception of stimuli during behavioural contexts associated with encountering dominant conspecifics.