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Active NON-SBIR/STTR RPGS NIH (US)

Synaptic circuit mechanisms underlying psilocybin's therapeutic effects in the stressed brain

$6.79M USD

Funder NATIONAL INSTITUTE OF MENTAL HEALTH
Recipient Organization University of California Santa Cruz
Country United States
Start Date Sep 25, 2024
End Date Jun 30, 2029
Duration 1,739 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 11048951
Grant Description

PROJECT SUMMARY Psychedelics are chemicals best known for their ability to induce profound changes in the human conscious experience. After a several-decade hiatus, research on psychedelics is undergoing a renaissance, driven by their potential to treat psychiatric disorders with rapid onset and enduring effect. Recent research

reveals that psychedelics can rapidly promote the structural and functional plasticity of synapses, leading to the conjecture that neural plasticity underlies their long-term therapeutic values. However, the neurobiological mechanisms remain largely elusive. Our overarching goal is to understand the cellular and circuit mechanisms

underlying psychedelics’ long-lasting therapeutic effects. In this proposal, we focus on the classical serotonergic psychedelic psilocybin and investigate how it rescues the deleterious effects of stress, a major risk factor for many neuropsychiatric disorders. Our central hypothesis is that psilocybin affects the brain at multiple levels,

from synaptic plasticity to the functional network; although psilocybin only transiently enhances synapse formation, it permanently alters the synaptic circuit in an experience-dependent manner; the incorporation of new synapses into the neural circuit is essential for psilocybin’s long-lasting rescue of stress-induced functional and

behavioral deficits. Specifically, in Aim 1, we will determine the acute and enduring effects of psilocybin on the stressed brain, particularly on the structural reorganization of synaptic circuits, on cortical functional networks, and on the representation of behavioral variables by cortical neuronal ensembles. Aim 2 determines how the

environmental and behavioral contexts in which psilocybin is administered impact its rescuing effects on the stressed brain. Aim 3 determines the contribution of psilocybin-induced neuroplasticity, particularly the stabilization of newly formed dendritic spines, to its rescuing effects on the stressed brain. Overall, these studies

will provide an integrated, mechanistic understanding of psilocybin’s rescuing effects across the organizational hierarchy of the brain, from molecules and synapses to circuits and functional networks, and lay the foundation for its clinical application in treating stress-related psychiatric disorders.

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University of California Santa Cruz

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