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Metabolomics and integrated network analysis reveal roles of endocannabinoids and large neutral amino acid balance in the ayahuasca experience.
Madrid-Gambin, Francisco; Gomez-Gomez, Alex; Busquets-Garcia, Arnau; Haro, Noemí; Marco, Santiago; Mason, Natasha L; Reckweg, Johannes T; Mallaroni, Pablo; Kloft, Lilian; van Oorsouw, Kim; Toennes, Stefan W; de la Torre, Rafael; Ramaekers, Johannes G; Pozo, Oscar J.
Afiliação
  • Madrid-Gambin F; Applied Metabolomics Research Group, IMIM-Institut Hospital del Mar d'Investigacions Mèdiques, 08003 Barcelona, Spain; Signal and Information Processing for Sensing Systems, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain. E
  • Gomez-Gomez A; Applied Metabolomics Research Group, IMIM-Institut Hospital del Mar d'Investigacions Mèdiques, 08003 Barcelona, Spain.
  • Busquets-Garcia A; Cell-type mechanisms in normal and pathological behavior Research Group, IMIM-Institut Hospital del Mar d'Investigacions Mèdiques, 08003 Barcelona, Spain.
  • Haro N; Applied Metabolomics Research Group, IMIM-Institut Hospital del Mar d'Investigacions Mèdiques, 08003 Barcelona, Spain.
  • Marco S; Signal and Information Processing for Sensing Systems, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology, 08028 Barcelona, Spain; Department of Electronics and Biomedical Engineering, Universitat de Barcelona, Barcelona 08028, Spain.
  • Mason NL; Department of Neuropsychology and Psychopharmacology, Faculty of Psychology and Neuroscience, Maastricht University, 6200 MD Maastricht, The Netherlands.
  • Reckweg JT; Department of Neuropsychology and Psychopharmacology, Faculty of Psychology and Neuroscience, Maastricht University, 6200 MD Maastricht, The Netherlands.
  • Mallaroni P; Department of Neuropsychology and Psychopharmacology, Faculty of Psychology and Neuroscience, Maastricht University, 6200 MD Maastricht, The Netherlands.
  • Kloft L; Department of Neuropsychology and Psychopharmacology, Faculty of Psychology and Neuroscience, Maastricht University, 6200 MD Maastricht, The Netherlands.
  • van Oorsouw K; Department of Clinical Psychological Science, Faculty of Psychology and Neuroscience, Maastricht University, 6200 MD Maastricht, The Netherlands.
  • Toennes SW; Institute of Legal Medicine, University Hospital, Goethe University, Frankfurt/Main, Germany.
  • de la Torre R; Integrative Pharmacology & Systems Neuroscience Group, IMIM-Institut Hospital del Mar d'Investigacions Mèdiques, 08003 Barcelona, Spain.
  • Ramaekers JG; Department of Neuropsychology and Psychopharmacology, Faculty of Psychology and Neuroscience, Maastricht University, 6200 MD Maastricht, The Netherlands.
  • Pozo OJ; Applied Metabolomics Research Group, IMIM-Institut Hospital del Mar d'Investigacions Mèdiques, 08003 Barcelona, Spain. Electronic address: opozo@imim.es.
Biomed Pharmacother ; 149: 112845, 2022 May.
Article em En | MEDLINE | ID: mdl-35339828
ABSTRACT
There has been a renewed interest in the potential use of psychedelics for the treatment of psychiatric conditions. Nevertheless, little is known about the mechanism of action and molecular pathways influenced by ayahuasca use in humans. Therefore, for the first time, our study aims to investigate the human metabolomics signature after consumption of a psychedelic, ayahuasca, and its connection with both the psychedelic-induced subjective effects and the plasma concentrations of ayahuasca alkaloids. Plasma samples of 23 individuals were collected both before and after ayahuasca consumption. Samples were analysed through targeted metabolomics and further integrated with subjective ratings of the ayahuasca experience (i.e., using the 5-Dimension Altered States of Consciousness Rating Scale [ASC]), and plasma ayahuasca-alkaloids using integrated network analysis. Metabolic pathways enrichment analysis using diffusion algorithms for specific KEGG modules was performed on the metabolic output. Compared to baseline, the consumption of ayahuasca increased N-acyl-ethanolamine endocannabinoids, decreased 2-acyl-glycerol endocannabinoids, and altered several large-neutral amino acids (LNAAs). Integrated network results indicated that most of the LNAAs were inversely associated with 9 out of the 11 subscales of the ASC, except for tryptophan which was positively associated. Several endocannabinoids and hexosylceramides were directly associated with the ayahuasca alkaloids. Enrichment analysis confirmed dysregulation in several pathways involved in neurotransmission such as serotonin and dopamine synthesis. In conclusion, a crosstalk between the circulating LNAAs and the subjective effects is suggested, which is independent of the alkaloid concentrations and provides insights into the specific metabolic fingerprint and mechanism of action underlying ayahuasca experiences.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Aminoácidos Neutros / Banisteriopsis / Endocanabinoides / Alucinógenos Limite: Humans Idioma: En Revista: Biomed Pharmacother Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Aminoácidos Neutros / Banisteriopsis / Endocanabinoides / Alucinógenos Limite: Humans Idioma: En Revista: Biomed Pharmacother Ano de publicação: 2022 Tipo de documento: Article