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Pharmahuasca: Human Pharmacology of Oral DMT Plus Harmine

Jonathan Ott

Journal of Psychoactive Drugs April 1, 1999 DOI: 10.1080/02791072.1999.10471741 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Review Peer reviewed
Sample size 8
Population Human self-experimenters
Topics Ayahuasca DMT
Keywords Harmine Tryptamines Hallucinogen Pharmacology Bioassay Harmaline Ingestion Monoamine oxidase Toxicology Traditional medicine
Citations 136
Key findings The Holmstedt-Lindgren hypothesis—that oral DMT is psychoactive due to MAO inhibition from co-ingested beta-carbolines—was confirmed by eight self-experimenters across roughly 70 bioassays.

Abstract

A summary is presented of human self-experiments or psychonautic bioassays of pharmahuasca--capsules containing crystalline N,N-dimethyltryptamine (DMT) plus harmine, as well as combinations of other psychoactive tryptamines with other beta-carbolines. The 1967 Holmstedt-Lindgren hypothesis of the ayahuasca effect--oral psychoactivity of DMT consequent to monoamine-oxidase (MAO) inhibition from simultaneous ingestion of beta-carbolines--has been confirmed by eight self-experimenters. Results of a total of some 70 bioassays are summarized and the literature on this subject is reviewed (with 66 references and one table).

Comparable studies

Other narrative reviews on DMT, most cited first.

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