Antidepressant Effects of a Single Dose of Ayahuasca in Patients With Recurrent Depression: A SPECT Study
Ayahuasca is an Amazonian botanical hallucinogenic brew which contains dimethyltryptamine, a 5-HT2A receptor agonist, and harmine, a monoamine-oxidase A inhibitor. Our group recently reported that ayahuasca administration was associated with fast-acting antidepressive effects in 6 depressive patient...
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Veröffentlicht in: | Journal of clinical psychopharmacology 2016-02, Vol.36 (1), p.77-81 |
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creator | Sanches, Rafael Faria de Lima Osório, Flávia Dos Santos, Rafael G Macedo, Ligia R H Maia-de-Oliveira, João Paulo Wichert-Ana, Lauro de Araujo, Draulio Barros Riba, Jordi Crippa, José Alexandre S Hallak, Jaime E C |
description | Ayahuasca is an Amazonian botanical hallucinogenic brew which contains dimethyltryptamine, a 5-HT2A receptor agonist, and harmine, a monoamine-oxidase A inhibitor. Our group recently reported that ayahuasca administration was associated with fast-acting antidepressive effects in 6 depressive patients. The objective of the present work was to assess the antidepressive potentials of ayahuasca in a bigger sample and to investigate its effects on regional cerebral blood flow. In an open-label trial conducted in an inpatient psychiatric unit, 17 patients with recurrent depression received an oral dose of ayahuasca (2.2 mL/kg) and were evaluated with the Hamilton Rating Scale for Depression, the Montgomery-Åsberg Depression Rating Scale, the Brief Psychiatric Rating Scale, the Young Mania Rating Scale, and the Clinician Administered Dissociative States Scale during acute ayahuasca effects and 1, 7, 14, and 21 days after drug intake. Blood perfusion was assessed eight hours after drug administration by means of single photon emission tomography. Ayahuasca administration was associated with increased psychoactivity (Clinician Administered Dissociative States Scale) and significant score decreases in depression-related scales (Hamilton Rating Scale for Depression, Montgomery-Åsberg Depression Rating Scale, Brief Psychiatric Rating Scale) from 80 minutes to day 21. Increased blood perfusion in the left nucleus accumbens, right insula and left subgenual area, brain regions implicated in the regulation of mood and emotions, were observed after ayahuasca intake. Ayahuasca was well tolerated. Vomiting was the only adverse effect recorded, being reported by 47% of the volunteers. Our results suggest that ayahuasca may have fast-acting and sustained antidepressive properties. These results should be replicated in randomized, double-blind, placebo-controlled trials. |
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Our group recently reported that ayahuasca administration was associated with fast-acting antidepressive effects in 6 depressive patients. The objective of the present work was to assess the antidepressive potentials of ayahuasca in a bigger sample and to investigate its effects on regional cerebral blood flow. In an open-label trial conducted in an inpatient psychiatric unit, 17 patients with recurrent depression received an oral dose of ayahuasca (2.2 mL/kg) and were evaluated with the Hamilton Rating Scale for Depression, the Montgomery-Åsberg Depression Rating Scale, the Brief Psychiatric Rating Scale, the Young Mania Rating Scale, and the Clinician Administered Dissociative States Scale during acute ayahuasca effects and 1, 7, 14, and 21 days after drug intake. Blood perfusion was assessed eight hours after drug administration by means of single photon emission tomography. Ayahuasca administration was associated with increased psychoactivity (Clinician Administered Dissociative States Scale) and significant score decreases in depression-related scales (Hamilton Rating Scale for Depression, Montgomery-Åsberg Depression Rating Scale, Brief Psychiatric Rating Scale) from 80 minutes to day 21. Increased blood perfusion in the left nucleus accumbens, right insula and left subgenual area, brain regions implicated in the regulation of mood and emotions, were observed after ayahuasca intake. Ayahuasca was well tolerated. Vomiting was the only adverse effect recorded, being reported by 47% of the volunteers. Our results suggest that ayahuasca may have fast-acting and sustained antidepressive properties. 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Our group recently reported that ayahuasca administration was associated with fast-acting antidepressive effects in 6 depressive patients. The objective of the present work was to assess the antidepressive potentials of ayahuasca in a bigger sample and to investigate its effects on regional cerebral blood flow. In an open-label trial conducted in an inpatient psychiatric unit, 17 patients with recurrent depression received an oral dose of ayahuasca (2.2 mL/kg) and were evaluated with the Hamilton Rating Scale for Depression, the Montgomery-Åsberg Depression Rating Scale, the Brief Psychiatric Rating Scale, the Young Mania Rating Scale, and the Clinician Administered Dissociative States Scale during acute ayahuasca effects and 1, 7, 14, and 21 days after drug intake. Blood perfusion was assessed eight hours after drug administration by means of single photon emission tomography. Ayahuasca administration was associated with increased psychoactivity (Clinician Administered Dissociative States Scale) and significant score decreases in depression-related scales (Hamilton Rating Scale for Depression, Montgomery-Åsberg Depression Rating Scale, Brief Psychiatric Rating Scale) from 80 minutes to day 21. Increased blood perfusion in the left nucleus accumbens, right insula and left subgenual area, brain regions implicated in the regulation of mood and emotions, were observed after ayahuasca intake. Ayahuasca was well tolerated. Vomiting was the only adverse effect recorded, being reported by 47% of the volunteers. Our results suggest that ayahuasca may have fast-acting and sustained antidepressive properties. These results should be replicated in randomized, double-blind, placebo-controlled trials.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Antidepressive Agents - administration & dosage</subject><subject>Antidepressive Agents - adverse effects</subject><subject>Antidepressive Agents - therapeutic use</subject><subject>Banisteriopsis - chemistry</subject><subject>Brain - blood supply</subject><subject>Brain - drug effects</subject><subject>Depressive Disorder, Major - drug therapy</subject><subject>Depressive Disorder, Major - physiopathology</subject><subject>Female</subject><subject>Hallucinogens - administration & dosage</subject><subject>Hallucinogens - adverse effects</subject><subject>Hallucinogens - therapeutic use</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Plant Preparations - administration & dosage</subject><subject>Plant Preparations - adverse effects</subject><subject>Plant Preparations - therapeutic use</subject><subject>Psychiatric Status Rating Scales</subject><subject>Recurrence</subject><subject>Time Factors</subject><subject>Tomography, Emission-Computed, Single-Photon</subject><subject>Treatment Outcome</subject><issn>0271-0749</issn><issn>1533-712X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1PwzAMhiMEYmPwDxDKkUtH0ny13KpufAmJiQ3BrUrbhAV17UjSw_49mTYQ4oIvlu3XryU_AJxjNMYoFVcP-WyMfgcl_AAMMSMkEjh-OwRDFAscIUHTAThx7gMhTEXMjsEg5pwFDzIEJmu9qdXaKudk6-FUa1V5BzsNJZyb9r1RcNI5tW1kG7nspaskNC2cSW9UG5Svxi_hs6p6a0MNJzsv07XXMIPz2TRfwLnv680pONKycepsn0fg5Wa6yO-ix6fb-zx7jCpCkY-kJEynEqu6RrLWWsg40aXgONaUEFoyGYa4RIwKQhjjvMYUJZxSWbGUYkJG4HLnu7bdZ6-cL1bGVappZKu63hU4wUyEZwn-v1QwzAXCIglSupNWtnPOKl2srVlJuykwKrY8isCj-MsjrF3sL_TlStU_S98AyBd78oQD</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>Sanches, Rafael Faria</creator><creator>de Lima Osório, Flávia</creator><creator>Dos Santos, Rafael G</creator><creator>Macedo, Ligia R H</creator><creator>Maia-de-Oliveira, João Paulo</creator><creator>Wichert-Ana, Lauro</creator><creator>de Araujo, Draulio Barros</creator><creator>Riba, Jordi</creator><creator>Crippa, José Alexandre S</creator><creator>Hallak, Jaime E C</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>20160201</creationdate><title>Antidepressant Effects of a Single Dose of Ayahuasca in Patients With Recurrent Depression: A SPECT Study</title><author>Sanches, Rafael Faria ; de Lima Osório, Flávia ; Dos Santos, Rafael G ; Macedo, Ligia R H ; Maia-de-Oliveira, João Paulo ; Wichert-Ana, Lauro ; de Araujo, Draulio Barros ; Riba, Jordi ; Crippa, José Alexandre S ; Hallak, Jaime E C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-aa35f9a1edd0adff7a28fb7612f4334b5a9a11b0547335566d1408644ac594133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Administration, Oral</topic><topic>Adult</topic><topic>Antidepressive Agents - administration & dosage</topic><topic>Antidepressive Agents - adverse effects</topic><topic>Antidepressive Agents - therapeutic use</topic><topic>Banisteriopsis - chemistry</topic><topic>Brain - blood supply</topic><topic>Brain - drug effects</topic><topic>Depressive Disorder, Major - drug therapy</topic><topic>Depressive Disorder, Major - physiopathology</topic><topic>Female</topic><topic>Hallucinogens - administration & dosage</topic><topic>Hallucinogens - adverse effects</topic><topic>Hallucinogens - therapeutic use</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Plant Preparations - administration & dosage</topic><topic>Plant Preparations - adverse effects</topic><topic>Plant Preparations - therapeutic use</topic><topic>Psychiatric Status Rating Scales</topic><topic>Recurrence</topic><topic>Time Factors</topic><topic>Tomography, Emission-Computed, Single-Photon</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sanches, Rafael Faria</creatorcontrib><creatorcontrib>de Lima Osório, Flávia</creatorcontrib><creatorcontrib>Dos Santos, Rafael G</creatorcontrib><creatorcontrib>Macedo, Ligia R H</creatorcontrib><creatorcontrib>Maia-de-Oliveira, João Paulo</creatorcontrib><creatorcontrib>Wichert-Ana, Lauro</creatorcontrib><creatorcontrib>de Araujo, Draulio Barros</creatorcontrib><creatorcontrib>Riba, Jordi</creatorcontrib><creatorcontrib>Crippa, José Alexandre S</creatorcontrib><creatorcontrib>Hallak, Jaime E C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of clinical psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sanches, Rafael Faria</au><au>de Lima Osório, Flávia</au><au>Dos Santos, Rafael G</au><au>Macedo, Ligia R H</au><au>Maia-de-Oliveira, João Paulo</au><au>Wichert-Ana, Lauro</au><au>de Araujo, Draulio Barros</au><au>Riba, Jordi</au><au>Crippa, José Alexandre S</au><au>Hallak, Jaime E C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antidepressant Effects of a Single Dose of Ayahuasca in Patients With Recurrent Depression: A SPECT Study</atitle><jtitle>Journal of clinical psychopharmacology</jtitle><addtitle>J Clin Psychopharmacol</addtitle><date>2016-02-01</date><risdate>2016</risdate><volume>36</volume><issue>1</issue><spage>77</spage><epage>81</epage><pages>77-81</pages><issn>0271-0749</issn><eissn>1533-712X</eissn><abstract>Ayahuasca is an Amazonian botanical hallucinogenic brew which contains dimethyltryptamine, a 5-HT2A receptor agonist, and harmine, a monoamine-oxidase A inhibitor. Our group recently reported that ayahuasca administration was associated with fast-acting antidepressive effects in 6 depressive patients. The objective of the present work was to assess the antidepressive potentials of ayahuasca in a bigger sample and to investigate its effects on regional cerebral blood flow. In an open-label trial conducted in an inpatient psychiatric unit, 17 patients with recurrent depression received an oral dose of ayahuasca (2.2 mL/kg) and were evaluated with the Hamilton Rating Scale for Depression, the Montgomery-Åsberg Depression Rating Scale, the Brief Psychiatric Rating Scale, the Young Mania Rating Scale, and the Clinician Administered Dissociative States Scale during acute ayahuasca effects and 1, 7, 14, and 21 days after drug intake. Blood perfusion was assessed eight hours after drug administration by means of single photon emission tomography. Ayahuasca administration was associated with increased psychoactivity (Clinician Administered Dissociative States Scale) and significant score decreases in depression-related scales (Hamilton Rating Scale for Depression, Montgomery-Åsberg Depression Rating Scale, Brief Psychiatric Rating Scale) from 80 minutes to day 21. Increased blood perfusion in the left nucleus accumbens, right insula and left subgenual area, brain regions implicated in the regulation of mood and emotions, were observed after ayahuasca intake. Ayahuasca was well tolerated. Vomiting was the only adverse effect recorded, being reported by 47% of the volunteers. Our results suggest that ayahuasca may have fast-acting and sustained antidepressive properties. These results should be replicated in randomized, double-blind, placebo-controlled trials.</abstract><cop>United States</cop><pmid>26650973</pmid><doi>10.1097/JCP.0000000000000436</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Adult Antidepressive Agents - administration & dosage Antidepressive Agents - adverse effects Antidepressive Agents - therapeutic use Banisteriopsis - chemistry Brain - blood supply Brain - drug effects Depressive Disorder, Major - drug therapy Depressive Disorder, Major - physiopathology Female Hallucinogens - administration & dosage Hallucinogens - adverse effects Hallucinogens - therapeutic use Humans Male Middle Aged Plant Preparations - administration & dosage Plant Preparations - adverse effects Plant Preparations - therapeutic use Psychiatric Status Rating Scales Recurrence Time Factors Tomography, Emission-Computed, Single-Photon Treatment Outcome |
title | Antidepressant Effects of a Single Dose of Ayahuasca in Patients With Recurrent Depression: A SPECT Study |
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