A Single Dose of 5-MeO-DMT Stimulates Cell Proliferation, Neuronal Survivability, Morphological and Functional Changes in Adult Mice Ventral Dentate Gyrus
Rafael Vitor Lima Da Cruz, Thiago C. Moulin, Lyvia Lintzmaier Petiz, Richardson N. Leão
Frontiers in Molecular Neuroscience September 4, 2018 DOI: 10.3389/fnmol.2018.00312 via OpenAlex
Summary
AI-generated from the abstractA 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.
Study at a glance
| Characteristics | Experimental study Peer reviewed |
|---|---|
| Population | Adult mice |
| Intervention | 5-MeO-DMT |
| Dose | a single intracerebroventricular (ICV) injection |
| Topics | Neuroplasticity |
| Keywords | Dentate gyrus Subgranular zone Bromodeoxyuridine Neuroscience |
| Citations | 86 |
| Key finding | A single ICV injection of 5-MeO-DMT increased the number of newborn dentate gyrus granule cells in adult mice and altered their dendritic morphology and electrophysiological properties. |
Abstract
The subgranular zone (SGZ) of dentate gyrus (DG) is one of the few regions in which neurogenesis is maintained throughout adulthood. It is believed that newborn neurons in this region encode temporal information about partially overlapping contextual memories. The 5-Methoxy-N,N-dimethyltryptamine (5-MeO-DMT) is a naturally occurring compound capable of inducing a powerful psychedelic state. Recently, it has been suggested that DMT analogs may be used in the treatment of mood disorders. Due to the strong link between altered neurogenesis and mood disorders, we tested whether 5-MeO-DMT is capable of increasing DG cell proliferation. We show that a single intracerebroventricular (ICV) injection of 5-MeO-DMT increases the number of Bromodeoxyuridine (BrdU+) cells in adult mice DG. Moreover, using a transgenic animal expressing tamoxifen-dependent Cre recombinase under doublecortin promoter, we found that 5 Meo-DMT treated mice had a higher number of newborn DG Granule cells (GC). We also showed that these DG GC have more complex dendritic morphology after 5-MeO-DMT. Lastly, newborn GC treated with 5-MeO-DMT, display shorter afterhyperpolarization (AHP) potentials and higher action potential (AP) threshold compared. Our findings show that 5-MeO-DMT affects neurogenesis and this effect may contribute to the known antidepressant properties of DMT-derived compounds.