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Psilocybin therapy

From Wikipedia, the free encyclopedia
Experimental use of psilocybin to treat anxiety & depression
Psilocybin-containing mushrooms

Psilocybin therapy (orpsilocybin-assisted therapy) is the use ofpsilocybin (the psychoactive ingredient inpsilocybin mushrooms) in treating a range of mental health conditions, such as depression, anxiety, addictions,[1]obsessive compulsive disorder (OCD), and psychosis.[2] It is one of several forms ofpsychedelic therapy under study. Psilocybin was popularized as a psychedelic recreational drug in the 1970s and was classified as a Schedule I drug by theDEA. Research on psilocybin as a medical treatment was restricted until the 1990s because of the sociocultural fear of dependence on this drug. As of 2022, psilocybin is the most commonly researched psychedelic due to its safety and low potential for abuse and dependence.[2] Clinical trials are being conducted at universities and there is evidence confirming the use of psilocybin in the treatment of depression,post-traumatic stress disorder (PTSD) and end of life anxiety.[3]

History

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The first historical record of psilocybin use dates back toMesoamerica. A Codex known as the "Yuta Tnoho" or "Vindobonensis Mexicanus I" that belonged to theMixtec culture in the 1500s BCE depicted religious and medicinal ritual ingestion of psilocybin-containing mushrooms.[1][4] Fungi were a prominent feature in Mixtec cultures, with over 5,000 different names of common edible mushrooms known across Mexican languages.[4]

Despite colonists' efforts to eradicate these ceremonies, ritualistic consumption ofPsilocybe mushrooms continues in modern spiritual and medicinal practice.[1] The hallucinations produced by the psilocybin induce a trance-like state that is believed to allow the soul to disconnect from the body, resulting in healing and spiritual enlightenment.[1]

Traditional psilocybin use was typically achieved through the consumption of dried or fresh psilocybin-containing mushrooms.[1] However, in 1959,Albert Hofmann, a Swiss chemist, became the first person toextract pure psilocybin from the mushroomPsilocybe mexicana.Sandoz, the company that employed Hofmann, then began to sell the active compound to clinicians as an aid inpsychedelic psychotherapy.[5]

Albert Hofmann's discovery of psilocybin played a pivotal role in catalyzing thePsychedelic Era, a cultural phenomenon that unfolded during the 1960s and 1970s. This era witnessed significant societal, musical, and artistic transformations, many of which were heavily influenced by the use of psychedelic substances, including psilocybin. At this time, though, there was very little known about psychedelics and their long-term effects.

In August 1960,Timothy Leary conducted a self-experiment using psilocybin mushrooms. After trying pure, extracted psilocybin, he andDr. Richard Alpert conducted research on whether it could help reducerecidivism rates and constitute an effective psychotherapy aid. In 1963, Leary and Alpert were suspended from their jobs atHarvard University, due to irresponsible and dangerous experimentation with psilocybin mushrooms.[6] Psilocybin research in the United States ended in 1970 when the use and possession of psilocybin mushrooms became illegal.[7][5]

In 2018–19, the United StatesFood and Drug Administration (FDA) grantedbreakthrough therapy designation to facilitate further research for psilocybin in the possible treatment ofdepressive disorders.[8]

Neuroscience and pharmacology

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Psilocybin is the main psychoactive compound in the mushroom genusPsilocybe. Psilocybin (O-phosphoryl-4-hydroxy-N,N-dimethyltryptamine) and its active metabolitepsilocin (4-hydroxy-N,N-dimethyltryptamine) are part of a group of tryptamine/indolamine hallucinogens that are related toserotonin.

Psilocybin is a prodrug for psilocin, meaning that psilocybin is de-phosphorylated in the GI tract of the body into psilocin so it can cross the blood-brain barrier. Psilocin is a selective agonist of the5-HT receptors, specifically 5-HT1A, 5-HT1B, 5-HT2A, 5-HT2B, and 5-HT2C.[9] Although to a lesser extent, psilocin also bonds to dopamine-3 receptors, which may aid in treating substance use disorders.[2] Further, psilocin has some effect on theamygdala andhypothalamus that aids incircadian rhythm regulation.[2]

Nausea, vomiting, muscle weakness, and lack of coordination are some of the physical side effects. Hallucinations and an inability to distinguish fiction from reality are among the psychological effects of psilocybin use. Panic attacks and psychotic-like episodes are also possible, especially if a large amount is consumed.[10]

Chemical compound of psilocin
Chemical compound of psilocybin

Research

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Use of psilocybin for treating depression is under preliminary research.[11] Evidence to date indicates that psilocybin therapy produces substantial reductions in depressive symptoms, formajor depressive disorder andtreatment-resistant depression, and also for depression associated with life-threatening cancer.[11] Similarly, psilocybin therapy has been found to increase rates ofremission from depression.[11]

Neural mechanisms

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Functional neuroimaging studies have explored potential neural mechanisms underlying psilocybin therapy's therapeutic effects, particularly in depression, anxiety and post-traumatic stress disorders.

One line of research has focused on thedefault mode network (DMN), a brain network involved in self-referential processing,autobiographical memory, and the sense of self, as playing a significant role in depression and anxiety.[12][13] Research usingfunctional magnetic resonance imaging (fMRI) has shown that psilocybin acutely reduces activity in the DMN, temporarily disrupting its connectivity patterns.[14][15][16] This disruption is associated with a breakdown of rigid, maladaptive patterns of thought often observed in mood disorders. Subsequent restoration of DMN connectivity has been correlated with improved clinical outcomes, suggesting a potential neural mechanism underlying the therapeutic effects of psilocybin.[17]

Psilocybin has also been shown to affect the amygdala, a brain region involved in emotional processing. Increased amygdala responsiveness to emotional stimuli, particularly fearful facial expressions, has been observed one day after treatment.[18] This increased responsiveness has been associated with reductions in depressive symptoms, suggesting that psilocybin may temporarily restore emotional sensitivity, which is often blunted in depression, post-traumatic stress disorder, and anxiety disorders.[19][20]

In addition, psilocybin has been found to enhancefunctional connectivity across variousbrain networks, promoting a more flexible and dynamic neural state.[21][22] This increased connectivity may support long-term changes in emotional and cognitive patterns associated with therapeutic outcomes.

Finally, psilocybin induces a temporary increase in brain entropy, reflecting a more diverse and disorganized pattern of brain activity.[16][23] This "entropic" state allows for a broader range of mental states and reduced dominance of habitual neural patterns, which may help disrupt maladaptive cognitive loops associated with depression and other mental health conditions.

Safety

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In the United States, psilocybin (along with other psychedelic drugs) has been heavily criminalized since the 1960s, classified as a Schedule I substance under the federalControlled Substances Act (Schedule I is defined as a substance having substantial potential for abuse, absence of adequate safety evidence, and no currently accepted clinical uses for therapy).[24] Prior to the 1960s, psychedelics were not considered "hard drugs", and were studied extensively for their immense medicinal potential for treating psychiatric disorders; the criminalization of psychedelics via their classification as Schedule I substances is inconsistent with over 70 years of scientific and medical research and was contrary to all available evidence at the time.[25] According to the largest controlled clinical study of psilocybin to date atKing's College London, volunteers who received doses of psilocybin experienced no serious adverse side effects, experiencing some changes in mood and perception but no negative effects on cognitive or emotional functioning.[26]

An important area of concern is identifying appropriate candidates for psilocybin therapy. In patients with depression, it is important to consider psychological, social, and biological factors. These factors may predispose them to negative reactions to the substance and result in adverse events.[citation needed] Research into the effects of psilocybin on those experiencing suicidality varies. While some research found that psilocybin therapy could be destabilizing and upsetting to these patients, other studies found psilocybin treatment resulted in reduced suicidal behavior and thoughts.[11]

Legal status

[edit]
See also:Legality of psilocybin mushrooms

In theUnited States, under theControlled Substances Act, psilocybin is classified as aSchedule I drug. Heroin and LSD are examples of Schedule I substances, which have a high potential for misuse and have no accepted medical use in the US.[27] They are currently petitions being made advocating for general considerations to sponsors developing psychedelic drugs for treatment of medical conditions (e.g., psychiatric disorders, substance use disorders).[28] For psychedelic drugs that are Schedule I controlled substances, activities associated with IND (Investigational New Drug) must comply with the applicableDrug Enforcement Administration (DEA) regulations for research, manufacturing, importation/exportation, handling, and storage.[28] Separately, while the use and possession of psilocybin in the United States is still illegal under federal law,[29] several U.S. cities and a few states have decriminalized its use.

InAustralia, authorized psychiatrists can prescribe psilocybin fortreatment-resistant depression.[30]

InCanada, beginning in 2020, some individuals with terminal illness experiencing end-of-life distress have been granted compassionate access to psilocybin-assisted therapy.[31] As of 2023, more than 50 Canadians have received psilocybin-assisted therapy on this basis.[32] In addition,Health Canada has allowed some health care professionals to use psilocybin mushrooms personally to help them develop future treatments.[33]

InGermany, two facilities are allowed to offer psilocybin to adults with treatment-resistant depression through a establishedcompassionate use program prior to regulatory approval.[34]

In theCzech Republic, a law was passed allowing trained psychiatrists to provide psilocybin therapy under appropriate conditions, if supporting psychotherapy is provided. It can be provided for depression, PTSD, and substance use disorders.[35]

InJamaica, psychedelic retreats such asMycoMeditations provide psilocybin therapy as a result of psilocybin being legal, as Jamaica has never criminalized or banned the possession and use ofpsilocybin mushrooms.

See also

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References

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  1. ^abcdeVan Court, R.C.; Wiseman, M.S.; Meyer, K.W.; Ballhorn, D.J.; Amses, K.R.; Slot, J.C.; Dentinger, B.T.M.; Garibay-Orijel, R.; Uehling, J.K. (April 2022)."Diversity, biology, and history of psilocybin-containing fungi: Suggestions for research and technological development".Fungal Biology.126 (4):308–319.Bibcode:2022FunB..126..308V.doi:10.1016/j.funbio.2022.01.003.PMID 35314062.
  2. ^abcdGeiger, Haden A.; Wurst, Madeline G.; Daniels, R. Nathan (2018-10-17)."DARK Classics in Chemical Neuroscience: Psilocybin".ACS Chemical Neuroscience.9 (10):2438–2447.doi:10.1021/acschemneuro.8b00186.ISSN 1948-7193.PMID 29956917.S2CID 49591766.
  3. ^Marks, Mason; Cohen, Glen (October 4, 2021)."Psychedelic therapy: A roadmap for wider acceptance and utilization".Nature Medicine.27 (10):1669–1671.doi:10.1038/s41591-021-01530-3.PMID 34608331.S2CID 238355863.
  4. ^abHernández-Santiago, Faustino; Martínez-Reyes, Magdalena; Pérez-Moreno, Jesús; Mata, Gerardo; Hernández-Santiago, Faustino; Martínez-Reyes, Magdalena; Pérez-Moreno, Jesús; Mata, Gerardo (2017)."Pictographic representation of the first dawn and its association with entheogenic mushrooms in a 16th century Mixtec Mesoamerican Codex".Revista mexicana de micología.46:19–28.ISSN 0187-3180.
  5. ^abDaniel, Jeremy; Haberman, Margaret (2018-03-23)."Clinical potential of psilocybin as a treatment for mental health conditions".The Mental Health Clinician.7 (1):24–28.doi:10.9740/mhc.2017.01.024.ISSN 2168-9709.PMC 6007659.PMID 29955494.
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  8. ^"FDA grants Breakthrough Therapy Designation to Usona Institute's psilocybin program for major depressive disorder".www.businesswire.com. 2019-11-22. Retrieved2019-11-25.
  9. ^Jann, Michael W (March 9, 2021)."Psilocybin Revisited: The Science Behind the Drug and Its Surprising Therapeutic Potential".Psychiatric Times.38 (3).
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  12. ^Davey, Christopher G.; Pujol, Jesus; Harrison, Ben J. (2016-05-15)."Mapping the self in the brain's default mode network".NeuroImage.132:390–397.doi:10.1016/j.neuroimage.2016.02.022.ISSN 1095-9572.PMID 26892855.
  13. ^Menon, Vinod (2023-08-16)."20 years of the default mode network: A review and synthesis".Neuron.111 (16):2469–2487.doi:10.1016/j.neuron.2023.04.023.ISSN 1097-4199.PMC 10524518.PMID 37167968.
  14. ^Carhart-Harris, Robin L.; Erritzoe, David; Williams, Tim; Stone, James M.; Reed, Laurence J.; Colasanti, Alessandro; Tyacke, Robin J.; Leech, Robert; Malizia, Andrea L.; Murphy, Kevin; Hobden, Peter; Evans, John; Feilding, Amanda; Wise, Richard G.; Nutt, David J. (2012-02-07)."Neural correlates of the psychedelic state as determined by fMRI studies with psilocybin".Proceedings of the National Academy of Sciences of the United States of America.109 (6):2138–2143.doi:10.1073/pnas.1119598109.ISSN 1091-6490.PMC 3277566.PMID 22308440.
  15. ^Tagliazucchi, Enzo; Carhart-Harris, Robin; Leech, Robert; Nutt, David; Chialvo, Dante R. (November 2014)."Enhanced repertoire of brain dynamical states during the psychedelic experience".Human Brain Mapping.35 (11):5442–5456.doi:10.1002/hbm.22562.ISSN 1097-0193.PMC 6869695.PMID 24989126.
  16. ^abSiegel, Joshua S.; et al. (2024)."Psilocybin desynchronizes the human brain".Nature.632 (8023):131–138.Bibcode:2024Natur.632..131S.doi:10.1038/s41586-024-07624-5.medRxiv 10.1101/2023.08.22.23294131.PMC 11291293.PMID 39020167.
  17. ^Carhart-Harris, Robin L.; Roseman, Leor; Bolstridge, Mark; Demetriou, Lysia; Pannekoek, J. Nienke; Wall, Matthew B.; Tanner, Mark; Kaelen, Mendel; McGonigle, John; Murphy, Kevin; Leech, Robert; Curran, H. Valerie; Nutt, David J. (2017-10-13)."Psilocybin for treatment-resistant depression: fMRI-measured brain mechanisms".Scientific Reports.7 (1): 13187.Bibcode:2017NatSR...713187C.doi:10.1038/s41598-017-13282-7.ISSN 2045-2322.PMC 5640601.PMID 29030624.
  18. ^Husain, Muhammad Ishrat; Ledwos, Nicole; Fellows, Elise; Baer, Jenna; Rosenblat, Joshua D.; Blumberger, Daniel M.; Mulsant, Benoit H.; Castle, David J. (2023-02-10)."Serotonergic psychedelics for depression: What do we know about neurobiological mechanisms of action?".Frontiers in Psychiatry.13 1076459.doi:10.3389/fpsyt.2022.1076459.ISSN 1664-0640.PMC 9950579.PMID 36844032.
  19. ^Kraehenmann, Rainer; Preller, Katrin H.; Scheidegger, Milan; Pokorny, Thomas; Bosch, Oliver G.; Seifritz, Erich; Vollenweider, Franz X. (2015-10-15)."Psilocybin-Induced Decrease in Amygdala Reactivity Correlates with Enhanced Positive Mood in Healthy Volunteers".Biological Psychiatry. Serotonin, Mood, and Anxiety.78 (8):572–581.doi:10.1016/j.biopsych.2014.04.010.ISSN 0006-3223.PMID 24882567.
  20. ^Zaretsky, Tamar Glatman; Jagodnik, Kathleen M.; Barsic, Robert; Antonio, Josimar Hernandez; Bonanno, Philip A.; MacLeod, Carolyn; Pierce, Charlotte; Carney, Hunter; Morrison, Morgan T.; Saylor, Charles; Danias, George; Lepow, Lauren; Yehuda, Rachel (2024)."The Psychedelic Future of Post-Traumatic Stress Disorder Treatment".Current Neuropharmacology.22 (4):636–735.doi:10.2174/1570159X22666231027111147.ISSN 1875-6190.PMC 10845102.PMID 38284341.
  21. ^Melani, Alice; Bonaso, Marco; Biso, Letizia; Zucchini, Benedetta; Conversano, Ciro; Scarselli, Marco (2025-01-19)."Uncovering Psychedelics: From Neural Circuits to Therapeutic Applications".Pharmaceuticals (Basel, Switzerland).18 (1): 130.doi:10.3390/ph18010130.ISSN 1424-8247.PMC 11769142.PMID 39861191.
  22. ^Gudmundsen, Frederik; Jessen, Naja Støckel; Baun, Christina; Herth, Matthias M.; Shalgunov, Vladimir; Fisher, Patrick MacDonald; Palner, Mikael (10 June 2024)."A single dose of psilocybin induces lasting changes in metabolic connectivity within biologically informed rat brain networks related to compulsions and anxiety".Mental Health Weekly Digest: 63.
  23. ^Carhart-Harris, Robin L.; Leech, Robert; Hellyer, Peter J.; Shanahan, Murray; Feilding, Amanda; Tagliazucchi, Enzo; Chialvo, Dante R.; Nutt, David (2014)."The entropic brain: a theory of conscious states informed by neuroimaging research with psychedelic drugs".Frontiers in Human Neuroscience.8: 20.doi:10.3389/fnhum.2014.00020.ISSN 1662-5161.PMC 3909994.PMID 24550805.
  24. ^"Psilocybin (magic mushrooms)". Drugs.com. 2021. Retrieved24 March 2021.
  25. ^Sproul, Conrad (2021).""Don't Kill My Buzz, Man!" - Explaining the Criminalization of Psychedelic Drugs".Oregon Undergraduate Research Journal.19 (1):1–53.doi:10.5399/uo/ourj.19.1.2.S2CID 237845545.
  26. ^"Magic mushroom compound psilocybin found safe for consumption in largest ever controlled study".The Independent. 2019-12-18. Retrieved2022-08-24.
  27. ^"Psilocybin Fast Facts".www.justice.gov. Retrieved2023-12-06.
  28. ^abResearch, Center for Drug Evaluation and (2023-06-26)."Psychedelic Drugs: Considerations for Clinical Investigations".www.fda.gov. Retrieved2023-12-06.
  29. ^"Psilocybin Fast Facts".www.justice.gov.
  30. ^Shepherd, Tory (2023-02-03)."Australia to allow prescription of MDMA and psilocybin for treatment-resistant mental illnesses".The Guardian.ISSN 0261-3077. Retrieved2023-10-26.
  31. ^Lindsay, Bethany (5 August 2020)."4 Canadians with terminal cancer win the right to try magic mushrooms".Canadian Broadcasting Corporation. Retrieved8 February 2026.
  32. ^Kratina, Sarah; Lo, Christopher; Strike, Carol; Schwartz, Robert; Rush, Brian (2023)."Psychedelics to Relieve Psychological Suffering Associated with a Life-Threatening Diagnosis: Time for a Canadian Policy Discussion".Healthcare Policy.18 (4).doi:10.12927/hcpol.2023.27048.PMC 10370393.PMID 37486818.
  33. ^Dubinski, Kate (10 December 2020)."Some doctors, therapists get Health Canada permission to use magic mushrooms".Canadian Broadcasting Corporation. Retrieved8 February 2026.
  34. ^"Germany Establishes EU's First Psilocybin Compassionate Access Program".Psychedelic Alpha. 2025-07-31. Retrieved2025-07-31.
  35. ^Madero, Santiago; Soto-Angona, Oscar; Ona, Genis; Sanchez-Moreno, Jose; Vieta, Eduard (2026)."Current perspectives on psychedelic treatments in Europe".The Lancet Regional Health – Europe.61: 101537.doi:10.1016/j.lanepe.2025.101537.PMC 12670272.PMID 41341075.{{cite journal}}: CS1 maint: article number as page number (link)
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