Serotonergic psychedelic 5-MeO-DMT alters plasticity-related gene expression and generates anxiolytic effects in stressed mice.
Margareth Nogueira, Daiane C Ferreira Golbert, Richardson Menezes, Raíssa Nóbrega de Almeida, Nicole Galvão-Coelho, Andressa N Siroky, Thiago Z Lima, Helton Maia, Katarina E. Leão, Richardson N. Leão
Molecular Psychiatry 2025 DOI: 10.1038/s41380-024-02655-w (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Experimental study Peer reviewed |
|---|---|
| Population | Mice |
| Intervention | 5-MeO-DMT |
| Dose | single dose |
| Duration | 1 hour, 5 hours, or 5 days |
| Topics | 5-MeO-DMT DMT Serotonin |
| Keywords | Psychopharmacology Anxiety research Natural compounds |
| Citations | 18 |
| Key findings | 5-MeO-DMT altered gene expression in brain regions linked to anxiety and, in mice subjected to acute stress, reduced corticosterone levels and produced robust anxiolytic effects. |
Abstract
Serotonergic psychedelics have potential therapeutic effects in treating anxiety and mood disorders, often after a single dose, and are suggested to have plasticity-inducing action. However, a comprehensive mechanism of action is still lacking. Here, we investigated how a single dose of the short-acting 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT) acts on gene expression from microdissected brain regions (anterior cingulate cortex - ACC; basolateral amygdala - BLA; ventral hippocampus CA1 region - vCA1 and dentate gyrus-DG) of naive and stressed mice. Specifically, we compared gene expression of Arc, Zif268, BDNF, CREB, mTORC1, NR2A, TRIP8b, and NFkB in mice injected with 5-MeO-DMT or saline at different time points (1 h, 5 h, or 5 days prior). 5-MeO-DMT altered mRNA expression of immediate early genes Arc and ZiF268 in the ACC, BLA, and vCA1, while NR2A expression was decreased after 5 h in the vCA1. We also found a long-term increase in TRIP8b, a gene related to the modulation of neuronal activity, in the vCA1 after 5 days. Behaviorally, 5-MeO-DMT treated mice showed mixed anxiolytic and anxiogenic effects in the elevated plus maze and open field test 24 h or 5 days after treatment. However, pre-treated mice subjected to acute stress showed both lower corticosterone levels and robust anxiolytic effects of 5-MeO-DMT administration. Together, our findings provide insights into the molecular actions of 5-MeO-DMT in the brain related to anxiolytic effects of behavior.