Evidence map›Paper›PMID 40498206›Full record

ArticleMetabolic brain disease2025

Immunomodulatory and behavioral effects of ayahuasca and N, N-dimethyltryptamine in a rat model of lipopolysaccharide-induced depression.

Daniel do Nascimento Sousa, Monique de Azevedo, Maria Lucília Santos, Tatiana Karla Dos Santos Borges, Daniela Mara de Oliveira, Eloisa Dutra Caldas

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Article in Metabolic brain disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Daniel do Nascimento SousaLaboratory of Toxicology, Department of Pharmacy, Faculty of Health Sciences, University of Brasília, Brasilia, DF, Brazil.ORCID 0000-0003-4259-6386
Monique de AzevedoDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasília, Brasilia, DF, Brazil.
Maria Lucília SantosChemistry Institute, University of Brasília, Brasilia, DF, Brazil.ORCID 0000-0002-0884-4211
Tatiana Karla Dos Santos BorgesLaboratory of Cellular Immunology, Pathology Area, Faculty of Medicine, University of Brasilia, Brasilia, DF, Brazil.ORCID 0000-0002-6813-6276
Daniela Mara de OliveiraDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasília, Brasilia, DF, Brazil.ORCID 0000-0002-2832-5726
Eloisa Dutra CaldasLaboratory of Toxicology, Department of Pharmacy, Faculty of Health Sciences, University of Brasília, Brasilia, DF, Brazil. eloisa@unb.br.ORCID 0000-0002-7197-6807

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ayahuasca (Aya) is an Amazonian beverage traditionally used as medicine by Indigenous people in South America to treat various illnesses and have shown a potential to treat depression. This study aimed to investigate the antidepressant effects of fluoxetine, Aya and N, N dimethyl tryptamine (DMT), a component of the beverage, focusing on the modulation of inflammatory serum cytokine profiles and behavior of Wistar rats subjected to lipopolysaccharide (LPS)-induced depression. In total, 126 rats were randomly assigned to seven groups: saline control, LPS, fluoxetine, three ayahuasca groups (dosed at 0.5, 1, and 2 times the usual ritualistic dose, Aya0.5, Aya1 and Aya2), and one DMT treatment group. The rats received LPS every other day from day 1 to 13 and fluoxetine, Aya and DMT daily from day 2 to 14. At day 15, the rats were submitted to open field and forced swimming tests, plasma samples were collected and the animals were euthanized. The LPS group showed lower body weight grain and higher plasma levels of pro-inflammatory cytokines IL-1α (p < 0.001), TNF-α, and IL-12p70 compared to control, which were significantly reduced by the treatment groups (p < 0.05 up to p < 0.0001), indicating a potential for modulation of the inflammatory state seen in depression. The Aya2 group exhibited increased locomotion in the open field arena compared to the fluoxetine (p < 0.05) and DMT (p < 0.01) groups, with a significantly higher percentage of entries into the center than the control group (p < 0.01). Furthermore, treatments with fluoxetine, Aya, and DMT significantly increased swimming time compared to the LPS group (p < 0.01), and fluoxetine and the Aya0.5 groups displayed higher climbing times compared to LPS and control (p < 0.05). Although the LPS model did not consistently induce depressive-like behaviors, the results highlight the potential of ayahuasca and DMT to modulate the immune system and reduce pro-inflammatory cytokine levels associated with depression, which could have significant implications for treating inflammation-related aspects of depression.

Indexed as

Antidepressive AgentsBanisteriopsisBehavior, AnimalDepressionImmunologic FactorsImmunomodulating AgentsN,N-DimethyltryptaminePlant ExtractsAnimalsCytokinesDisease Models, AnimalFluoxetineLipopolysaccharidesMaleRatsRats, WistarAntidepressive AgentsCytokinesFluoxetineImmunologic FactorsImmunomodulating AgentsLipopolysaccharidesN,N-DimethyltryptaminePlant ExtractsAyahuascaBehaviorCytokinesDepressionDMTLPS-induced depressive rats

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.