Rafael G. dos Santos, Juliana Mendes Rocha, Giordano Novak Rossi, Flávia L. Osório, Genís Ona, José Carlos Bouso, Gabriela de Oliveira Silveira, Mauricio Yonamine, Camila Marchioni, Eduardo José Crevelin, Maria Eugênia Queiroz, José Alexandre Crippa, Jaime E. C. Hallak
{"title":"死藤水对健康志愿者和社交焦虑症志愿者内源性大麻素系统的影响:来自两个试点、概念验证、随机、安慰剂对照试验的结果","authors":"Rafael G. dos Santos, Juliana Mendes Rocha, Giordano Novak Rossi, Flávia L. Osório, Genís Ona, José Carlos Bouso, Gabriela de Oliveira Silveira, Mauricio Yonamine, Camila Marchioni, Eduardo José Crevelin, Maria Eugênia Queiroz, José Alexandre Crippa, Jaime E. C. Hallak","doi":"10.1002/hup.2834","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Objective</h3>\n \n <p>To assess endocannabinoid (anandamide, AEA; 2-arachidonoylglycerol, 2-AG) plasma levels in healthy volunteers and in volunteers with social anxiety disorder (SAD) after a single oral dose of ayahuasca or placebo.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p><i>Post hoc</i> analysis of endocannabinoid plasma levels (baseline, 90 and 240 min after drug intake) from two parallel-group, randomized, placebo-controlled trials. In Study 1, 20 healthy volunteers ingested ayahuasca (average 1.58 mg/ml dimethyltryptamine (DMT)) or placebo, and in Study 2, 17 volunteers with SAD received ayahuasca (average 0.680 mg/ml DMT) or placebo.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>A significant difference was observed in AEA concentrations in Study 2 after ayahuasca intake (Χ<sup>2</sup>(2) = 6.5, <i>p</i> = 0.03, Friedman test), and near significant differences (increases) were observed between baseline and 90 (Z = 0, <i>p</i> = 0.06, Wilcoxon test) and 240 (Z = 10, <i>p</i> = 0.06) minutes after ayahuasca intake.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>Although our findings suggest that ayahuasca could modulate AEA levels in SAD patients, the high interindividual variability in both trials and the small samples preclude definitive conclusions. More research with larger samples is needed to better understand the effects of ayahuasca and other hallucinogens in the endocannabinoid system.</p>\n </section>\n </div>","PeriodicalId":13030,"journal":{"name":"Human Psychopharmacology: Clinical and Experimental","volume":"37 4","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2022-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":"{\"title\":\"Effects of ayahuasca on the endocannabinoid system of healthy volunteers and in volunteers with social anxiety disorder: Results from two pilot, proof-of-concept, randomized, placebo-controlled trials\",\"authors\":\"Rafael G. dos Santos, Juliana Mendes Rocha, Giordano Novak Rossi, Flávia L. Osório, Genís Ona, José Carlos Bouso, Gabriela de Oliveira Silveira, Mauricio Yonamine, Camila Marchioni, Eduardo José Crevelin, Maria Eugênia Queiroz, José Alexandre Crippa, Jaime E. C. 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引用次数: 6
摘要
目的评价内源性大麻素(anandamide, AEA);2-花生四烯醇甘油酯(2-AG)在健康志愿者和患有社交焦虑症(SAD)的志愿者口服单剂量死水或安慰剂后的血浆水平。方法对两个平行组、随机、安慰剂对照试验的内源性大麻素血浆水平(服药后基线、服药后90分钟和服药后240分钟)进行事后分析。在研究1中,20名健康志愿者服用死水(平均1.58 mg/ml二甲色胺(DMT))或安慰剂,在研究2中,17名患有SAD的志愿者服用死水(平均0.680 mg/ml DMT)或安慰剂。结果研究2中服用死藤水后AEA浓度差异有统计学意义(Χ2(2) = 6.5, p = 0.03, Friedman检验),且与服用死藤水后90分钟(Z = 0, p = 0.06, Wilcoxon检验)和240分钟(Z = 10, p = 0.06)相比差异接近统计学意义(增加)。虽然我们的研究结果表明死藤水可以调节SAD患者的AEA水平,但两项试验的高个体间差异和小样本排除了明确的结论。为了更好地了解死藤水和其他致幻剂对内源性大麻素系统的影响,需要更多的研究和更大的样本。
Effects of ayahuasca on the endocannabinoid system of healthy volunteers and in volunteers with social anxiety disorder: Results from two pilot, proof-of-concept, randomized, placebo-controlled trials
Objective
To assess endocannabinoid (anandamide, AEA; 2-arachidonoylglycerol, 2-AG) plasma levels in healthy volunteers and in volunteers with social anxiety disorder (SAD) after a single oral dose of ayahuasca or placebo.
Methods
Post hoc analysis of endocannabinoid plasma levels (baseline, 90 and 240 min after drug intake) from two parallel-group, randomized, placebo-controlled trials. In Study 1, 20 healthy volunteers ingested ayahuasca (average 1.58 mg/ml dimethyltryptamine (DMT)) or placebo, and in Study 2, 17 volunteers with SAD received ayahuasca (average 0.680 mg/ml DMT) or placebo.
Results
A significant difference was observed in AEA concentrations in Study 2 after ayahuasca intake (Χ2(2) = 6.5, p = 0.03, Friedman test), and near significant differences (increases) were observed between baseline and 90 (Z = 0, p = 0.06, Wilcoxon test) and 240 (Z = 10, p = 0.06) minutes after ayahuasca intake.
Conclusions
Although our findings suggest that ayahuasca could modulate AEA levels in SAD patients, the high interindividual variability in both trials and the small samples preclude definitive conclusions. More research with larger samples is needed to better understand the effects of ayahuasca and other hallucinogens in the endocannabinoid system.
期刊介绍:
Human Psychopharmacology: Clinical and Experimental provides a forum for the evaluation of clinical and experimental research on both new and established psychotropic medicines. Experimental studies of other centrally active drugs, including herbal products, in clinical, social and psychological contexts, as well as clinical/scientific papers on drugs of abuse and drug dependency will also be considered. While the primary purpose of the Journal is to publish the results of clinical research, the results of animal studies relevant to human psychopharmacology are welcome. The following topics are of special interest to the editors and readers of the Journal:
-All aspects of clinical psychopharmacology-
Efficacy and safety studies of novel and standard psychotropic drugs-
Studies of the adverse effects of psychotropic drugs-
Effects of psychotropic drugs on normal physiological processes-
Geriatric and paediatric psychopharmacology-
Ethical and psychosocial aspects of drug use and misuse-
Psychopharmacological aspects of sleep and chronobiology-
Neuroimaging and psychoactive drugs-
Phytopharmacology and psychoactive substances-
Drug treatment of neurological disorders-
Mechanisms of action of psychotropic drugs-
Ethnopsychopharmacology-
Pharmacogenetic aspects of mental illness and drug response-
Psychometrics: psychopharmacological methods and experimental design