Treating Drug Addiction With Ibogaine
By: David Bradley
Chemical intervention in the treatment of drug and alcohol addiction
There is not much in the plant world that
people have not sniffed, snorted, smoked, rubbed in, injected or
attempted to get inside their bodies in other ways in the hope of
eliciting someone kind of magical response. The well-known plants that
gave a positive result in the primitive tests - the coca plant,
poppies, marijuana, tobacco, betel trees, coffee beans - have since
grown infamous leaving the air heavy with their tragic scent in so many
places.
If plants are our downfall, then they might also be our salvation. An African shrub - Tabernanthe iboga - related to the coffee plant, offers some kind of hope for those who are addicted to alkaloid charms. Iboga has, like countless other herbal products, been used in traditional ceremonies and medicine for hundreds, if not thousands of years. In particular, in tropical West Africa it is a well-known hallucinogen used in male rites of passage but also as a tool by hunter to increase awareness and allow them to remain very still for prolonged periods. The physiologically active compound is an indole alkaloid called ibogaine*. Surprisingly though, ibogaine is not itself addictive and even more intriguing is that it seems to have anti-addictive qualities. Take this drug and it apparently cures addiction to another.
The main claim made by advocates of
ibogaine for treating drug addiction is that one dose is generally
enough. With ibogaine, there is no need for weeks and weeks of regular
methadone to stave off the chilling withdrawal symptoms of heroin, nor
the increasing possibility of addiction to the treatment itself
emerging. The fear of the detoxification process is claimed by drug
rehabilitation centres to be the major obstacle to most addicts beating
their habit. One dose - or at the most intermittent doses for two years
- can it is claimed remove the destructive addiction of several hard
drugs - cocaine and heroin, for instance - but even alcohol and
nicotine. It is especially effective in those who actually want to give up.
NDA International convinced several
researchers to take a close look at ibogaine's effects on opiates
several years ago. One of the scientists Stanley Glick, at Albany
Medical College found that in lab rats treated with ibogaine before a
morphine injection, the release of the neurotransmitter dopamine was
partially blocked. (Dopamine is thought to be responsible for
reinforcing the pleasurable effects of drugs of abuse.) Glick also
discovered that following ibogaine injection, rats with free access to
morphine cut down on their intake and had less withdrawal symptoms.
No definitive mode of action of ibogaine's supposed anti-addiction properties has yet been described. The molecular basis for addiction itself is not understood so this is unsurprising. However, ibogaine is known to be antagonistic to N-methyl-D-aspartate (NMDA) receptors. These receptors are thought to mediate some of the acute effects of drugs of abuse but by blocking them one may block the development of compulsive drug seek and taking. Ibogaine also seems to have activity in many neurotransmitter systems including serotonin uptake sites and sigma sites. It might be that its complexity of action has something to do with its activity. To confuse the picture still further there is also a putative long-lasting metabolite, O-desmethylibogaine which has not been investigated closely yet. However, according to Piotr Popik a psychopharmacologist at the Institute of Pharmacology, Polish Academy of Sciences, Kraków, working mainly on the mode of action of "anti-addictive" drugs, The NMDA antagonistic actions are enough to explain most of the 'anti-addictive' effects of ibogaine.'
Not all scientists are convinced of the
healing properties of those suffering addiction. Among ibogaine's
side-effects are ataxia (loss of muscle coordination), nausea, vomiting
and raised blood pressure. The compound also causes tremors,
hallucinations and apprehension. Moreover, there is still the death to
consider in the cancelled FDA trials.
Popik is somewhat sceptical of ibogaine's
potential. Popik co-authored the review with Glick. He points out that
ibogaine is not in fact unique, 'All of the known antagonists of the
NMDA receptor produce 'anti-addictive' effects in animal models of
compulsive drug seeking and taking.' A simple test he and his
colleagues carried out demonstrated that ibogaine is indeed an NMDA
antagonist but the fact is there are countless other less harmful
compounds with this same activity. Ibogaine
produces a lot of neuropathological changes in the cerebellum, Popik
adds. 'Briefly: I would not give it to my mother!' he told Catalyst.
Meanwhile, Glick's team at Albany Medical College has developed a
synthetic iboga alkaloid 18-methoxycoronaridine (18-MC). Their animal
tests show that 18-MC has similar activity to ibogaine but may not have
ibogaine's hallucinogenic properties.
The extraction of ibogaine from the roots and bark of Tabernanthe were first described in JACS in 1958 and its synthesis again in JACS in 1966, these classic recipes
have quickly found their way out of the student locker and into
Internet folklore, just as have methods for making fireworks and LSD.
Aside from growing interest sparked by the Internet, ibogaine does not
seem to have made its way on to the streets. Drug-pushers are perhaps
wary of selling something that could cut their markets for other drugs
in one fell swoop.
Something is also keeping ibogaine from
the medical mainstream. Could it be that the authorities believe the
existence an anti-addictive would actually increase drug abuse as users
would experiment keenly, knowing that a quick and easy escape route was
available to them. With the UK government revealing results of research
that show heroin use is spreading out from the inner cities and into
the shires, and the Home Office predicting an epidemic of addiction, it
is perhaps time to take a closer look at the weapons we use to wage the
war on drugs.
- ibogaine: 7-Ethyl-6,2,7,8,9,10,12,13-octahydro-2-methoxy-6,9-methano 5H-pyrido(1',2':1,2- azepine(4,5-)indole. It also goes by the name of NIH 10567 and Endabuse.
- The first report of the putative anti-addictive properties: Dzoljic ED, Kaplan CD, Dzoljic MR, Effects of Ibogaine on Naloxone-Precipitated Withdrawal Syndrome in Chronic Morphine- Dependent Rats, Archive of International Pharmacodynamics, 1988, 294, 64-70.
- Further reading: P. Popik and P. Skolnick, 'Pharmacology of Ibogaine and Ibogaine-Related Alkaloids', The Alkaloids, Academic Press, 1998, pp. 197-231.
You can read a news update on ibogaine in the forthcoming issue (#43) of Reactive Reports.
Read about the latest addiction therapy research via our PubMed rss feed.


