Decoupling of cortical activity from behavioral state following administration of the classic psychedelic DOI.

Classic psychedelics like DOI cause lasting changes in experience and show promise for treating depression. In the medial prefrontal cortex of male mice, DOI reduced low-frequency brain waves during rest, preventing the usual synchronization that occurs in less active states. It also increased gamma activity and suppressed fast-spiking neurons both during active and rest periods. These results suggest that DOI induces persistent desynchronization in the medial prefrontal cortex, which may contribute to the longer-lasting effects of psychedelics on brain plasticity and their therapeutic properties.

Study at a glance

Abstract

Administration or consumption of classic psychedelics (CPs) leads to profound changes in experience which are often described as highly novel and meaningful. They have shown substantial promise in treating depressive symptoms and may be therapeutic in other situations. Although research suggests that the therapeutic response is correlated with the intensity of the experience, the neural circuit basis for the alterations in experience caused by CPs requires further study. The medial prefrontal cortex (mPFC), where CPs have been shown to induce rapid, 5-HT2A receptor-dependent structural and neurophysiological changes, is believed to be a key site of action. To investigate the acute neural circuit changes induced by CPs, we recorded single neurons and local field potentials in the mPFC of freely behaving male mice after administration of the 5-HT2A/2C receptor-selective CP, 2,5-Dimethoxy-4-iodoamphetamine (DOI). We segregated recordings into active and rest periods in order to examine cortical activity during desynchronized (active) and synchronized (rest) states. We found that DOI induced a robust decrease in low frequency power when animals were at rest, attenuating the usual synchronization that occurs during less active behavioral states. DOI also increased broadband gamma power and suppressed activity in fast-spiking neurons in both active and rest periods. Together, these results suggest that the CP DOI induces persistent desynchronization in mPFC, including during rest when mPFC typically exhibits more synchronized activity. This shift in cortical dynamics may in part underlie the longer-lasting effects of CPs on plasticity, and may be critical to their therapeutic properties.