Home Ischemic Stroke Psilocybin improves mood, motor symptoms in patients with Parkinson’s disease

Psilocybin improves mood, motor symptoms in patients with Parkinson’s disease

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Key takeaways:

  • Treatment with psilocybin led to improvement in motor, non-motor and psychiatric symptoms for up to 1 month.
  • Results suggest that psilocybin therapy in PD warrants further investigation, researchers wrote.

Treatment with psilocybin was linked to improvements in motor and
non-motor symptoms of Parkinson’s disease, as well as associated
psychiatric conditions, with sustained results up to 1 month, results of
a pilot study show.

“Basic science discoveries have generated a lot of enthusiasm about the potential of psychedelics for Parkinson’s,” Ellen Bradley, MD,
assistant professor, department of psychiatry and behavioral sciences,
Weill Institute for Neurosciences at the University of California, San
Francisco, told Healio.

Data were derived from Bradley ER, et al. Neuropsychopharmacology. 2025;doi:10.1038/s41386-025-02097-0.

“We’ve lacked even initial safety data in humans with PD, or any
other neurodegenerative disorder. That’s the major gap we wanted to fill
in this first phase of work,” Bradley said.

Although psychiatric issues such as anxiety and depression
often accompany a diagnosis of PD and presage functional decline,
effective treatments are few, Bradley and colleagues wrote. Psilocybin
has demonstrated some success in treatment of anxiety and depression,
but its potential in PD is still unknown.

The open-label pilot study examined the safety, efficacy and
tolerability of psilocybin in 12 individuals (mean age 63.2 ± 8.2 years;
58.3% men) diagnosed with mild to moderate PD plus anxiety and/or
depression. Three initial enrollees were not treated with dopaminergic
drugs for PD-related motor symptoms, with nine patients prescribed a
stable carbidopa-levodopa regimen.

All participants received two doses of synthetic psilocybin: a single
10 mg dose followed by one 25 mg dose 2 weeks later, provided the first
dose was well-tolerated. Eight sessions of one-to-one psychotherapy
interspersed before, during and after dosing accompanied the treatments.

Vitals were assessed at baseline, then at irregular intervals up to
420 minutes after each psilocybin dose, under medical supervision.

Subjective drug experience was measured by the 5-Dimensional Altered
States of Consciousness (5D-ASC) scale. Safety and tolerability with
respect to PD symptoms were measured at 1 week after the 10 mg dose and 1
week and 1 one month following the 25 mg dose using the Movement
Disorder Society Unified Parkinson’s Disease Rating Scale (MDS-UPDRS).

Anxiety was tracked with the Hamilton Anxiety Rating Scale (HAM-A)
and depression by the Montgomery-Asberg Depression Rating Scale (MADRS).

According to results, patients did not report any serious adverse
events or medical interventions that required dosing adjustments. No
symptoms of psychosis were worsened. Treatment-emergent adverse events
occurred in 10 participants, with the most frequent being anxiety,
nausea and increased blood pressure.

Ellen Bradley

The researchers additionally reported that participants’ subjective
experience trended higher after the 25 mg dose compared with the 10 mg
dose, but not significantly so. Analysis of 5D-ASC scores from the pilot
study compared with a previous trial of 25 mg psilocybin therapy for
major depressive disorder indicated higher subjective intensity for
those enrolled in the pilot study.

Bradley and colleagues also reported significant improvement in both
motor symptoms (MDS-UPDRS Part II) and non-motor symptoms (MDS-UPDRS
Part I) at the 1-month follow up, -7.5 points and -13.75 points,
respectively.

Data further showed anxiety (HAM-A) and depression (MADRS) were improved at 1 week post treatment,
with depression significantly lessened at 1 month whereas anxiety was
not; improvements for both conditions, however, were sustained up to 3
months after dosing. Mean change from baseline to 90-day follow up were
-3.83 points and -9.33 points, respectively.

Results from the pilot, Bradley and colleagues wrote, suggest that
psilocybin therapy in PD warrants further investigation. A randomized
controlled trial, based at UCSF, is scheduled to expand to a second site
at Yale University, with a goal of enrolling 100 participants,
according to a release related to the study.

“These findings are exciting, but we can’t draw conclusions from a
small pilot. We’re now on to the next phase, conducting a much larger
trial designed to test efficacy and figure out psilocybin’s mechanisms
of action in PD,” Bradley told Healio. “The goal is to get more
targeted, effective treatment options in patients’ hands as quickly as
possible.

Reference:

How ‘magic mushrooms’ could help Parkinson’s disease patients. https://www.eurekalert.org/news-releases/1082246. Published April 29, 2025. Accessed May 2, 2025.

For more information:

Ellen Bradley, MD, can be reached at ellen.bradley@ucsf.edu and on LinkedIn here. 



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