DARK Classics in Chemical Neuroscience: Ibogaine
Michael Wasko, Paula A. Witt‐enderby, Christopher K. Surratt
ACS Chemical Neuroscience September 14, 2018 DOI: 10.1021/acschemneuro.8b00294 via OpenAlex
Summary
AI-generated from the abstractIbogaine, the main psychoactive alkaloid in the West African iboga plant, has a long history of ceremonial use and was once sold as an antidepressant in France before being withdrawn due to adverse effects. In the 1960s, U.S. heroin addicts reported that ibogaine cured their opiate addictions, and animal studies showed it reduces self-administration of opiates, cocaine, amphetamines, and nicotine. Ibogaine has moderate-to-weak affinity for many receptor and transporter proteins, and recent evidence suggests its actions at nicotinic acetylcholine receptor subtypes may explain its antiopiate effects. However, at micromolar levels ibogaine is neurotoxic and cardiotoxic, linked to several deaths.
Study at a glance
| Characteristics | Review Peer reviewed |
|---|---|
| Interventions | Ibogaine 18-methoxycoronaridine (18-MC) |
| Keywords | Hallucinogen Nicotine Synthetic cannabinoids Nicotinic acetylcholine receptor Nicotinic agonist |
| Citations | 63 |
| Key finding | Ibogaine's actions at nicotinic acetylcholine receptor subtypes may underlie its antiopiate effects, and the analog 18-MC retains anticraving properties with reduced toxicity. |
Abstract
The West African iboga plant has been used for centuries by the Bwiti and Mbiri tribes to induce hallucinations during religious ceremonies. Ibogaine, the principal alkaloid responsible for iboga's psychedelic properties, was isolated and sold as an antidepressant in France for decades before its adverse effects precipitated its removal from the market. An ibogaine resurgence in the 1960s was driven by U.S. heroin addicts who claimed that ibogaine cured their opiate addictions. Behavioral pharmacologic studies in animal models provided evidence that ibogaine could blunt self-administration of not only opiates but cocaine, amphetamines, and nicotine. Ibogaine displays moderate-to-weak affinities for a wide spectrum of receptor and transporter proteins; recent work suggests that its actions at nicotinic acetylcholine receptor subtypes may underlie its reputed antiopiate effects. At micromolar levels, ibogaine is neurotoxic and cardiotoxic and has been linked to several deaths by cardiac arrest. Structure-activity studies led to the isolation of the ibogaine analog 18-methoxycoronaridine (18-MC), an α3β4 nicotinic receptor modulator that retains ibogaine's anticraving properties with few or no adverse effects. Clinical trials of 18-MC treatment of nicotine addiction are pending. Ibogaine analogs may also hold promise for treating anxiety and depression via the "psychedelic-assisted therapy" approach that employs hallucinogens including psilocybin and methylenedioxymethamphetamine ("ecstasy").