Neuropsychopharmacology
February 18, 2026
Itishree Sahoo, Sairam Masadi, Ashwath Maheswari et al.
3 citations
Adolescent mice given psilocybin every other day from postnatal days 40-50 showed long-term changes in brain structure and function when tested in adulthood. Brain imaging revealed reduced volume and altered water diffusivity in several regions, with males more affected than females. Functional connectivity increased globally and regionally, notably between the prefrontal cortex and hypothalamus, thalamus, and midbrain. Mice showed reduced brain sensitivity to rewarding and aversive odors, and males had lower levels of epigenetic and neuroplasticity protein markers in the prefrontal cortex. Behaviorally, female mice showed reduced mobility in the open field test, while no differences appeared in the light/dark box test. These findings indicate that adolescent psilocybin exposure produces lasting developmental consequences, especially in males.
bioRxiv (Cold Spring Harbor Laboratory)
February 6, 2025
Bryce Axe, Ashwath Maheswari, Reagan Walhof et al.
3 citations
preprint
Repetitive mild head injuries from sports, accidents, or military service cause lasting cognitive, motor, and behavioral problems and raise the risk of dementia, Parkinson's disease, and chronic traumatic encephalopathy, yet no approved treatment exists. Testing the psychedelic psilocybin in adult female rats with mild repetitive head injury, the authors report that psilocybin reduces vasogenic edema, restores normal vascular reactivity and functional connectivity, reduces buildup of phosphorylated tau, increases levels of brain-derived neurotrophic factor and its receptor TrkB, and modulates lipid signaling molecules. These findings suggest psilocybin may have healing effects on head injury-related brain damage.
Neuroscience bulletin
May 21, 2026
Noah Cavallaro, Priya Rai, David Akins et al.
Mescaline, a psychedelic used ceremonially for thousands of years, produces distinct brain effects that differ from LSD and psilocybin. In awake rats, mescaline suppressed BOLD signal in the cerebellum, suggesting it disconnects this region from forebrain areas. However, resting-state scans showed the cerebellum became hyperconnected to the hippocampus, thalamus, somatosensory cortex, and midbrain. Mescaline also eliminated normal brain responses to rewarding smells, indicating disrupted sensory processing. Acoustic startle tests revealed frequency-dependent effects: enhancement at 4 kHz (+27.6%) and 20 kHz (+27.3%), but impairment at 12 kHz (-16.4%). The cerebellum may act as a dysregulated sensory filter, flooding forebrain circuits with unprocessed information, potentially explaining psychedelic-induced perceptual changes.