TY - JOUR
T1 - Dose-dependent changes in global brain activity and functional connectivity following exposure to psilocybin
T2 - a BOLD MRI study in awake rats
AU - Fuini, Evan
AU - Chang, Arnold
AU - Ortiz, Richard J.
AU - Nasseef, Taufiq
AU - Edwards, Josh
AU - Latta, Marc
AU - Gonzalez, Elias
AU - Woodward, Taylor J.
AU - Axe, Bryce
AU - Maheswari, Ashwath
AU - Cavallaro, Noah
AU - Bradshaw, Heather B.
AU - Kulkarni, Praveen P.
AU - Ferris, Craig F.
N1 - Publisher Copyright:
Copyright © 2025 Fuini, Chang, Ortiz, Nasseef, Edwards, Latta, Gonzalez, Woodward, Axe, Maheswari, Cavallaro, Bradshaw, Kulkarni and Ferris.
PY - 2025
Y1 - 2025
N2 - Psilocybin is a hallucinogen with complex neurobiological and behavioral effects. This is the first study to use MRI to follow functional changes in brain activity in response to different doses of psilocybin in fully awake, drug naive rats. We hypothesized that psilocybin would show a dose-dependent increase in activity in the prefrontal cortex and thalamus, while decreasing hippocampal activity. Female and male rats were given IP injections of vehicle or psilocybin in doses of 0.03 mg/kg, 0.3 mg/kg, and 3.0 mg/kg while fully awake during the imaging session. These levels were validated by measuring psilocybin and its metabolite, psilocin. Changes in BOLD signal were recorded over a 20 min window. Data for resting state functional connectivity were collected approximately 35 min post injection. All data were registered to rat 3D MRI atlas with 169 brain areas providing site-specific changes in global brain activity and changes in functional connectivity. Treatment with psilocybin resulted in a significant dose-dependent increase in positive BOLD signal. The areas most affected by the acute presentation of psilocybin were the somatosensory cortex, basal ganglia and thalamus. Males and females showed different sensitivity to psilocybin dose, with females exhibiting greater activation than males at 0.3 mg/kg, especially in thalamic and basal ganglia regions. There was a significant dose-dependent global increase in functional connectivity, highlighted by hyperconnectivity to the cerebellum. Brain areas hypothesized to be involved in loss of sensory filtering and organization of sensory motor stimuli, such as the cortico-striato-thalamo-cortical circuit and the claustrum, showed increased activation at higher doses of psilocybin. Indeed, the general neuroanatomical circuitry associated with the psychedelic experience was affected but the direction of the BOLD signal and pattern of activity between neural networks was inconsistent with the human literature.
AB - Psilocybin is a hallucinogen with complex neurobiological and behavioral effects. This is the first study to use MRI to follow functional changes in brain activity in response to different doses of psilocybin in fully awake, drug naive rats. We hypothesized that psilocybin would show a dose-dependent increase in activity in the prefrontal cortex and thalamus, while decreasing hippocampal activity. Female and male rats were given IP injections of vehicle or psilocybin in doses of 0.03 mg/kg, 0.3 mg/kg, and 3.0 mg/kg while fully awake during the imaging session. These levels were validated by measuring psilocybin and its metabolite, psilocin. Changes in BOLD signal were recorded over a 20 min window. Data for resting state functional connectivity were collected approximately 35 min post injection. All data were registered to rat 3D MRI atlas with 169 brain areas providing site-specific changes in global brain activity and changes in functional connectivity. Treatment with psilocybin resulted in a significant dose-dependent increase in positive BOLD signal. The areas most affected by the acute presentation of psilocybin were the somatosensory cortex, basal ganglia and thalamus. Males and females showed different sensitivity to psilocybin dose, with females exhibiting greater activation than males at 0.3 mg/kg, especially in thalamic and basal ganglia regions. There was a significant dose-dependent global increase in functional connectivity, highlighted by hyperconnectivity to the cerebellum. Brain areas hypothesized to be involved in loss of sensory filtering and organization of sensory motor stimuli, such as the cortico-striato-thalamo-cortical circuit and the claustrum, showed increased activation at higher doses of psilocybin. Indeed, the general neuroanatomical circuitry associated with the psychedelic experience was affected but the direction of the BOLD signal and pattern of activity between neural networks was inconsistent with the human literature.
KW - 5-HT receptor
KW - BOLD resting state functional connectivity
KW - cerebellar nuclei
KW - hyperconnectivity
KW - psilocin
UR - https://www.scopus.com/pages/publications/105005222924
U2 - 10.3389/fnins.2025.1554049
DO - 10.3389/fnins.2025.1554049
M3 - Article
AN - SCOPUS:105005222924
SN - 1662-4548
VL - 19
JO - Frontiers in Neuroscience
JF - Frontiers in Neuroscience
M1 - 1554049
ER -