A single injection of the psychedelic compound 5-MeO-DMT into the brain's fluid-filled spaces increased the production of new neurons in the dentate gyrus of adult mice. Treated mice had more newborn granule cells, and these cells developed more complex branch-like structures. The new neurons also showed shorter afterhyperpolarization potentials and higher action potential thresholds, indicating altered electrical properties. These effects on neurogenesis may help explain the potential antidepressant actions of DMT-like compounds.
This is a correction notice for a previously published article. It does not present new findings or arguments. The notice corrects errors in the original paper, specifically in the Materials and Methods section regarding the number of animals used per group and in the Results section regarding the number of animals per group for behavioral tests.
A single dose of the psychedelic DMT reversed depression-like behaviors and cognitive impairments in mice exposed to chronic stress, outperforming the standard antidepressant fluoxetine. When given during stress, DMT prevented anhedonia but not cognitive deficits. DMT remained effective even under anesthesia, suggesting its therapeutic action does not require the psychedelic experience. All DMT regimens increased the integration of adult-born granule cells in the brain and reduced abnormal cell integration. The findings position DMT as a promising rapid-acting antidepressant that works through structural brain repair.