DMT and ayahuasca

DMT (N,N-dimethyltryptamine) is a psychedelic molecule of the tryptamine family, found in many plants and animals [1]. Ayahuasca is a traditional Amazonian brew that contains DMT along with other plant compounds that make it active when swallowed. So DMT vs ayahuasca is a single molecule whose effects last minutes against a plant preparation whose effects last several hours.

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3D model of DMT
DMT

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DMT vs ayahuasca: what is the difference?

DMT is a defined chemical. Ayahuasca is a plant decoction whose make-up varies with the species used and how it is prepared [2] [3].

  • Plants. The best-known recipe combines the vine Banisteriopsis caapi, which supplies the harmala alkaloids (harmine, harmaline and tetrahydroharmine), with leaves of Psychotria viridis, which supply the DMT [2].
  • Why they are combined. Swallowed alone, DMT is broken down by the enzyme MAO in the gut and liver; the harmala alkaloids inhibit MAO-A and let it reach the bloodstream [3] [4].
  • Duration. Given intravenously, DMT acts within seconds and wears off within minutes [5]. Ayahuasca takes longer to start and its effects last about four hours [6] [7].
  • Risks. Because it contains MAO inhibitors, ayahuasca carries interaction risks that inhaled or injected DMT does not share to the same degree [8].

So findings for one cannot simply be carried over to the other.

What is DMT- or ayahuasca-assisted therapy?

Staged re-enactment of a research session: a person lies on a clinical bed wearing eyeshades under a blanket, accompanied by a researcher seated alongside, in a softly lit room with plants.

Re-enactment of a session in a DMT study (research setting)

It is a research protocol that combines careful medical screening, one or a few sessions with the substance in a controlled setting, and support from trained staff [9].

It includes preparation beforehand and integration sessions afterwards. For now it exists only in clinical studies: neither is authorised as a medicine in the European Union [10].

What is the history of DMT and ayahuasca?

Old sepia portrait of Richard Spruce, an elderly man with a white beard, spectacles and a pale brimmed hat.

Richard Spruce, botanist who studied ayahuasca in the Amazon

Ayahuasca has a long history of traditional and religious use; DMT was only synthesised in the 20th century and studied in people from the 1950s.

  • Traditional use. Indigenous peoples of the Amazon basin use ayahuasca for healing and spiritual purposes [7].
  • 1931. The chemist Richard Manske synthesises DMT, without testing its effects in humans [11].
  • 1930s. Ayahuasca enters religious use in Brazil; several syncretic churches now take it as a sacrament [7] [3].
  • 1946. Oswaldo Gonçalves de Lima identifies DMT in a plant while studying the “jurema wine” of the Pankararu people of Pernambuco [12].
  • 1956. The Hungarian psychiatrist Stephen Szára describes the psychedelic effects of DMT after injecting himself [13].
  • 1971. DMT is placed in Schedule I of the UN Convention on Psychotropic Substances [14].
  • 1994. Rick Strassman, in the United States, publishes studies of intravenous DMT in volunteers [15].
  • 2015–2026. Clinical studies in depression: ayahuasca in Brazil [16] [7] and DMT in the UK [9].

How do DMT and ayahuasca work?

Ribbon diagram of human monoamine oxidase A (PDB 2BXS), in blue, red and green, anchored to the outer mitochondrial membrane, with the FAD cofactor and an inhibitor bound at its centre.

Monoamine oxidase A, MAO-A (molecular structure)

DMT acts mainly on the serotonin 5-HT2A receptor, the shared target of the classic psychedelics [17]. The body clears it very quickly, which is why the effect of an injection is so brief [9].

In ayahuasca, the harmala alkaloids block the breakdown of DMT mainly in the gut and liver; the effects track the rise of DMT in the blood [6].

Imaging and EEG studies show changes in brain activity during the experience [18] [19]. They describe what changes in the brain, but do not yet explain why symptoms improve.

How are study sessions run?

Sessions take place in hospital or research settings, after a medical assessment and under continuous supervision.

  • Ayahuasca. A single dose in a quiet, dimly lit room with music chosen in advance; investigators close by and a further psychiatric assessment at the end [7].
  • Intravenous DMT. An overnight hospital stay, preparation with two therapists the day before, a short infusion with the therapists present, and integration sessions over the following days and weeks [9].
  • Medication. Psychiatric medicines are stopped weeks before the session, with a longer gap for MAO inhibitors [9].
  • Other forms. Inhaled DMT [8] and continuous infusion, which extends the experience [20], are also being studied.

Which conditions are they being researched in?

Depression is the most researched area, with both ayahuasca and DMT. The studies are still small and short.

DMT and ayahuasca: conditions under research
ConditionWhere it has been studiedEvidencePhase
Treatment-resistant depressionAyahuasca in Brazil [7]; inhaled DMT [8]Controlled trials, still limitedPhase 2
Major depressive disorderIntravenous DMT in the UK [9]Controlled trials, still limitedPhase 2
Recurrent depressionAyahuasca in Brazil, open-label studies [16] [19]PreliminaryExploratory
AddictionHypothesis from members of ayahuasca churches [3]No clinical trialsExploratory

In the controlled trials, symptoms improved more than with placebo over the following days and weeks [7] [9]. A secondary analysis also reported less suicidal ideation, which needs confirming [21].

What are the risks and interactions?

In clinical settings, side effects were mostly short-lived. The most serious risk is ayahuasca interacting with antidepressants.

  • Ayahuasca. Nausea and vomiting are common [7]; blood pressure may rise slightly [6].
  • Intravenous DMT. Pain at the infusion site, nausea, short-lived anxiety and transient rises in blood pressure and heart rate, with no serious adverse events in the trial [9] [15].
  • Interactions. Combined with serotonergic antidepressants, the MAO inhibitors in ayahuasca can cause serotonin syndrome, which may be serious [22]. Any medicine or supplement should be reviewed by a doctor.
  • Who is left out. Studies exclude people with psychosis or bipolar disorder (personal or family history), pregnancy, significant physical illness or suicide risk; safety in these groups is unknown [7] [9] [23].
  • Outside clinical settings. In a large international survey, most people who had drunk ayahuasca reported acute physical effects, mainly vomiting, and a small minority later needed medical care [24]. In a brew prepared outside a study, the make-up is unknown [3].

What is still being researched

The next studies aim to confirm the early results and answer practical questions.

  • Whether the results hold up in larger, longer trials [7] [9].
  • How long any benefit lasts [9].
  • How much of the effect reflects expectation, since the effects are hard to mask [30].
  • What part psychological support plays in the outcome [9].
  • Whether what is learnt from pure DMT applies to ayahuasca, whose composition varies [3].
  • How both behave in people currently excluded from studies and in those taking other medicines.

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References

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  1. Cameron LP, Olson DE. Dark classics in chemical neuroscience: N,N-dimethyltryptamine (DMT). ACS Chem Neurosci. 2018;9(10):2344–2357. doi:10.1021/acschemneuro.8b00101 (opens in a new tab)Review
  2. McKenna DJ, Towers GH, Abbott F. Monoamine oxidase inhibitors in South American hallucinogenic plants: tryptamine and beta-carboline constituents of ayahuasca. J Ethnopharmacol. 1984;10(2):195–223. doi:10.1016/0378-8741(84)90003-5 (opens in a new tab)Study
  3. McKenna DJ. Clinical investigations of the therapeutic potential of ayahuasca: rationale and regulatory challenges. Pharmacol Ther. 2004;102(2):111–129. doi:10.1016/j.pharmthera.2004.03.002 (opens in a new tab)Review
  4. Callaway JC, McKenna DJ, Grob CS, et al. Pharmacokinetics of Hoasca alkaloids in healthy humans. J Ethnopharmacol. 1999;65(3):243–256. doi:10.1016/s0378-8741(98)00168-8 (opens in a new tab)Study
  5. Strassman RJ, Qualls CR, Uhlenhuth EH, Kellner R. Dose-response study of N,N-dimethyltryptamine in humans. II. Subjective effects and preliminary results of a new rating scale. Arch Gen Psychiatry. 1994;51(2):98–108. doi:10.1001/archpsyc.1994.03950020022002 (opens in a new tab)Clinical trial
  6. Riba J, Valle M, Urbano G, et al. Human pharmacology of ayahuasca: subjective and cardiovascular effects, monoamine metabolite excretion, and pharmacokinetics. J Pharmacol Exp Ther. 2003;306(1):73–83. doi:10.1124/jpet.103.049882 (opens in a new tab)Clinical trial
  7. Palhano-Fontes F, Barreto D, Onias H, et al. Rapid antidepressant effects of the psychedelic ayahuasca in treatment-resistant depression: a randomized placebo-controlled trial. Psychol Med. 2019;49(4):655–663. doi:10.1017/S0033291718001356 (opens in a new tab)Clinical trial
  8. Falchi-Carvalho M, Palhano-Fontes F, Wießner I, et al. Rapid and sustained antidepressant effects of vaporized N,N-dimethyltryptamine: a phase 2a clinical trial in treatment-resistant depression. Neuropsychopharmacology. 2025;50(6):895–903. doi:10.1038/s41386-025-02091-6 (opens in a new tab)Clinical trial
  9. Erritzoe D, Barba T, Benway T, et al. A short-acting psychedelic intervention for major depressive disorder: a phase IIa randomized placebo-controlled trial. Nat Med. 2026;32:591–598. doi:10.1038/s41591-025-04154-z (opens in a new tab)Clinical trial
  10. European Medicines Agency. Medicines data download (human medicines: authorised, refused, withdrawn and under evaluation), consulted October 2026: no medicine containing DMT or ayahuasca listed. ema.europa.eu (opens in a new tab)Regulatory source
  11. Manske RHF. A synthesis of the methyltryptamines and some derivatives. Can J Res. 1931;5(5):592–600. doi:10.1139/cjr31-097 (opens in a new tab)Study
  12. Barker SA. N,N-Dimethyltryptamine (DMT), an endogenous hallucinogen: past, present, and future research to determine its role and function. Front Neurosci. 2018;12:536. doi:10.3389/fnins.2018.00536 (opens in a new tab)Review
  13. Szára S. Dimethyltryptamin: its metabolism in man; the relation to its psychotic effect to the serotonin metabolism. Experientia. 1956;12(11):441–442. doi:10.1007/BF02157378 (opens in a new tab)Study
  14. United Nations. Convention on Psychotropic Substances, 1971 (Vienna), with its schedules as amended. unodc.org (PDF) (opens in a new tab)Legislation
  15. Strassman RJ, Qualls CR. Dose-response study of N,N-dimethyltryptamine in humans. I. Neuroendocrine, autonomic, and cardiovascular effects. Arch Gen Psychiatry. 1994;51(2):85–97. doi:10.1001/archpsyc.1994.03950020009001 (opens in a new tab)Clinical trial
  16. Osório FL, Sanches RF, Macedo LR, et al. Antidepressant effects of a single dose of ayahuasca in patients with recurrent depression: a preliminary report. Braz J Psychiatry. 2015;37(1):13–20. doi:10.1590/1516-4446-2014-1496 (opens in a new tab)Clinical trial
  17. Nichols DE. Psychedelics. Pharmacol Rev. 2016;68(2):264–355. doi:10.1124/pr.115.011478 (opens in a new tab)Review
  18. Timmermann C, Roseman L, Schartner M, et al. Neural correlates of the DMT experience assessed with multivariate EEG. Sci Rep. 2019;9:16324. doi:10.1038/s41598-019-51974-4 (opens in a new tab)Study
  19. Sanches RF, de Lima Osório F, Dos Santos RG, et al. Antidepressant effects of a single dose of ayahuasca in patients with recurrent depression: a SPECT study. J Clin Psychopharmacol. 2016;36(1):77–81. doi:10.1097/JCP.0000000000000436 (opens in a new tab)Clinical trial
  20. Luan LX, Eckernäs E, Ashton M, et al. Psychological and physiological effects of extended DMT. J Psychopharmacol. 2024;38(1):56–67. doi:10.1177/02698811231196877 (opens in a new tab)Study
  21. Zeifman RJ, Singhal N, Dos Santos RG, et al. Rapid and sustained decreases in suicidality following a single dose of ayahuasca among individuals with recurrent major depressive disorder: results from an open-label trial. Psychopharmacology (Berl). 2021;238(2):453–459. doi:10.1007/s00213-020-05692-9 (opens in a new tab)Study
  22. Callaway JC, Grob CS. Ayahuasca preparations and serotonin reuptake inhibitors: a potential combination for severe adverse interactions. J Psychoactive Drugs. 1998;30(4):367–369. doi:10.1080/02791072.1998.10399712 (opens in a new tab)Study
  23. Johnson MW, Richards WA, Griffiths RR. Human hallucinogen research: guidelines for safety. J Psychopharmacol. 2008;22(6):603–620. doi:10.1177/0269881108093587 (opens in a new tab)Guidance
  24. Bouso JC, Andión Ó, Sarris JJ, et al. Adverse effects of ayahuasca: results from the Global Ayahuasca Survey. PLOS Glob Public Health. 2022;2(11):e0000438. doi:10.1371/journal.pgph.0000438 (opens in a new tab)Study
  25. International Narcotics Control Board. Green List: list of psychotropic substances under international control, in accordance with the Convention on Psychotropic Substances of 1971. 36th edition, 2025 (DMT listed in Schedule I). incb.org (opens in a new tab)Regulatory source
  26. International Narcotics Control Board. Report of the International Narcotics Control Board for 2010 (E/INCB/2010/1). Paragraphs 284–287 (plant material containing psychoactive substances) and 500 (Brazil, ayahuasca for religious purposes). incb.org (PDF) (opens in a new tab)Regulatory source
  27. Decreto-Lei n.º 15/93, de 22 de Janeiro: regime jurídico do tráfico e consumo de estupefacientes e substâncias psicotrópicas (tabelas anexas), na redacção actual, incluindo as alterações da Lei n.º 23/2025. (Decree-Law 15/93 of 22 January: Portugal’s legal regime on trafficking and use of narcotic and psychotropic substances (annexed schedules), as currently amended, including by Law 23/2025.) diariodarepublica.pt (versão consolidada) (opens in a new tab)Legislation
  28. Lei n.º 30/2000, de 29 de Novembro: regime jurídico aplicável ao consumo de estupefacientes (descriminalização do consumo; não legaliza as substâncias). (Law 30/2000 of 29 November: the legal regime for drug use in Portugal (decriminalises personal use; does not legalise the substances).) diariodarepublica.pt (PDF) (opens in a new tab)Legislation
  29. Conselho Nacional de Políticas sobre Drogas (CONAD, Brasil). Resolução n.º 1, de 25 de Janeiro de 2010, sobre o uso religioso da ayahuasca; citada como referência na ata da 1.ª reunião ordinária do CONAD de 2025 (Ministério da Justiça e Segurança Pública). (Brazil’s National Council on Drug Policy (CONAD). Resolution No. 1 of 25 January 2010 on the religious use of ayahuasca; cited as the reference in the minutes of CONAD’s first ordinary meeting of 2025 (Ministry of Justice and Public Security).) gov.br (PDF) (opens in a new tab)Regulatory source
  30. Muthukumaraswamy SD, Forsyth A, Lumley T. Blinding and expectancy confounds in psychedelic randomized controlled trials. Expert Rev Clin Pharmacol. 2021;14(9):1133–1152. doi:10.1080/17512433.2021.1933434 (opens in a new tab)Review