4.3 Article

Changes in inflammatory biomarkers are related to the antidepressant effects of Ayahuasca

Journal

JOURNAL OF PSYCHOPHARMACOLOGY
Volume 34, Issue 10, Pages 1125-1133

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/0269881120936486

Keywords

BDNF; biomarkers; cortisol; immune system; psychedelics

Funding

  1. Brazilian National Council for Scientific and Technological Development (CNPq) [466760/2014, 479466/2013]
  2. CAPES Foundation within the Brazilian Ministry of Education [1677/2012, 1577/2013]
  3. National Science and Technology Institute for Translational Medicine [INCT-TM Fapesp 2014/50891-1, CNPq 465458/2014-9]
  4. CAPES Foundation from Brazilian Ministry of Education [88887.466701/2019-00]
  5. NHMRC [APP1125000]

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Background: Ayahuasca is a traditional Amazon brew and its potential antidepressant properties have recently been explored in scientific settings. We conducted a double-blind placebo-controlled trial of ayahuasca with treatment-resistant depression patients (n= 28) and healthy controls (n= 45). Aims: We are evaluating the blood inflammatory biomarkers: C-reactive protein and interleukin 6, as a potential consequence of ayahuasca intake and their correlation with serum cortisol and brain-derived neurotrophic factor levels. Blood samples were collected at pre-treatment and 48 hours after substance ingestion to assess the concentration of inflammatory biomarkers, together with administration of the Montgomery-angstrom sberg Depression Rating Scale. Results: At pre-treatment, patients showed higher C-reactive protein levels than healthy controls and a significant negative correlation between C-reactive protein and serum cortisol levels was revealed (rho= -0.40,n= 14). C-reactive protein in those patients was not correlated with Montgomery-angstrom sberg Depression Rating Scale scores. We observed a significant reduction of C-reactive protein levels across time in both patients and controls treated with ayahuasca, but not with placebo. Patients treated with ayahuasca showed a significant correlation (rho= + 0.57) between larger reductions of C-reactive protein and lower depressive symptoms at 48 hours after substance ingestion (Montgomery-angstrom sberg Depression Rating Scale). No significant result with respect to interleukin 6 and brain-derived neurotrophic factor was found. Furthermore, these biomarkers did not predict the antidepressant response or remission rates observed. Conclusions: These findings enhance the understanding of the biological mechanisms behind the observed antidepressant effects of ayahuasca and encourage further clinical trials in adults with depression.

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