{"id":2801,"date":"2025-09-02T23:59:15","date_gmt":"2025-09-02T23:59:15","guid":{"rendered":"https:\/\/naturalscience.com.co\/?p=2801"},"modified":"2025-09-15T12:52:31","modified_gmt":"2025-09-15T12:52:31","slug":"working-late","status":"publish","type":"post","link":"https:\/\/naturalscience.com.co\/en\/working-late\/","title":{"rendered":"Psilocybin with psychological support for treatment-resistant depression: an open-label feasibility study"},"content":{"rendered":"<h2 class=\"wp-block-heading\">Summary<\/h2>\n\n\n\n<p>Background Psilocybin is a serotonin receptor agonist that occurs naturally in some mushroom species. Recent<br>studies have assessed the therapeutic potential of psilocybin for various conditions, including end-of-life anxiety,<br>obsessive-compulsive disorder, and smoking and alcohol dependence, with promising preliminary results. Here, we<br>aimed to investigate the feasibility, safety, and effi cacy of psilocybin in patients with unipolar treatment-resistant<br>depression.<br>Methods In this open-label feasibility trial, 12 patients (six men, six women) with moderate-to-severe, unipolar,<br>treatment-resistant major depression received two oral doses of psilocybin (10 mg and 25 mg, 7 days apart) in a<br>supportive setting. There was no control group. Psychological support was provided before, during, and after each<br>session. The primary outcome measure for feasibility was patient-reported intensity of psilocybin\u2019s eff ects. Patients<br>were monitored for adverse reactions during the dosing sessions and subsequent clinic and remote follow-up.<br>Depressive symptoms were assessed with standard assessments from 1 week to 3 months after treatment, with the<br>16-item Quick Inventory of Depressive Symptoms (QIDS) serving as the primary effi cacy outcome. This trial is<br>registered with ISRCTN, number ISRCTN14426797.<br>Findings Psilocybin\u2019s acute psychedelic eff ects typically became detectable 30\u201360 min after dosing, peaked 2\u20133 h<br>after dosing, and subsided to negligible levels at least 6 h after dosing. Mean self-rated intensity (on a 0\u20131 scale)<br>was 0\u00b751 (SD 0\u00b736) for the low-dose session and 0\u00b775 (SD 0\u00b727) for the high-dose session. Psilocybin was well<br>tolerated by all of the patients, and no serious or unexpected adverse events occurred. The adverse reactions we<br>noted were transient anxiety during drug onset (all patients), transient confusion or thought disorder (nine patients),<br>mild and transient nausea (four patients), and transient headache (four patients). Relative to baseline, depressive<br>symptoms were markedly reduced 1 week (mean QIDS diff erence \u201311\u00b78, 95% CI \u20139\u00b715 to \u201314\u00b735, p=0\u00b7002, Hedges\u2019<br>g=3\u00b71) and 3 months (\u20139\u00b72, 95% CI \u20135\u00b769 to \u201312\u00b771, p=0\u00b7003, Hedges\u2019 g=2) after high-dose treatment. Marked and<br>sustained improvements in anxiety and anhedonia were also noted.<br>Interpretation This study provides preliminary support for the safety and effi cacy of psilocybin for treatment-resistant<br>depression and motivates further trials, with more rigorous designs, to better examine the therapeutic potential of<br>this approach.<br>Funding Medical Research Council. Copyright \u00a9 Carhart-Harris et al. Open Access article distributed under the terms of CC BY.<\/p>","protected":false},"excerpt":{"rendered":"<p>Summary Background Psilocybin is a serotonin receptor agonist that occurs naturally in some mushroom species. Recentstudies have assessed the therapeutic potential of psilocybin for various conditions, including end-of-life anxiety,obsessive-compulsive disorder, and smoking and alcohol dependence, with promising preliminary results. Here, weaimed to investigate the feasibility, safety, and effi cacy of psilocybin in patients with unipolar [&hellip;]<\/p>","protected":false},"author":1,"featured_media":2703,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":["post-2801","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-toxicologia-en-microdosis"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/posts\/2801","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/comments?post=2801"}],"version-history":[{"count":2,"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/posts\/2801\/revisions"}],"predecessor-version":[{"id":2911,"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/posts\/2801\/revisions\/2911"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/media\/2703"}],"wp:attachment":[{"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/media?parent=2801"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/categories?post=2801"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/naturalscience.com.co\/en\/wp-json\/wp\/v2\/tags?post=2801"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}