Ayahuasca compound changes brainwaves to vivid 'waking-dream' state

November 19, 2019

Science Daily/Imperial College London

Scientists have peered inside the brain to show how taking DMT affects human consciousness by significantly altering the brain's electrical activity.

DMT (or dimethyltryptamine) is one of the main psychoactive constituents in ayahuasca, the psychedelic brew traditionally made from vines and leaves of the Amazon rainforest. The drink is typically prepared as part of a shamanic ceremony and associated with unusual and vivid visions or hallucinations.

The latest study is the first to show how the potent psychedelic changes our waking brain waves -- with researchers comparing its powerful effects to 'dreaming while awake'.

The work, led by researchers from the Centre for Psychedelic Research at Imperial College London and published today in the journal Scientific Reports, may help to explain why people taking DMT and ayahuasca experience intense visual imagery and immersive 'waking-dream' like experiences.

DMT is a naturally occurring chemical found in miniscule amounts in the human brain but also in larger amounts in a number of plant species around the world.

Accounts from people who have taken DMT report intense visual hallucinations often accompanied by strong emotional experiences and even 'breakthroughs' into what users describe as an alternate reality or dimension.

But scientists are interested in using the powerful psychoactive compound for research as it produces relatively short but intense psychedelic experiences, providing a window for collecting data on brain activity when consciousness is profoundly altered.

In the latest study, the Imperial team captured EEG measures from healthy participants in a clinical setting, in a placebo-controlled design.

A total of 13 participants were given an intravenous infusion of DMT at the National Institute for Health Research (NIHR) Imperial Clinical Research Facility.

Volunteers were fitted with caps with electrodes to measure the brain's electrical activity, before, during and after their infusion, with the peak of the psychedelic experience lasting around 10 minutes.

Analysis revealed that DMT significantly altered electrical activity in the brain, characterised by a marked drop off in alpha waves -- the human brain's dominant electrical rhythm when we are awake. They also found a short-lived increase in brainwaves typically associated with dreaming, namely, theta waves.

In addition to changes in the types of brainwaves, they also found that, overall, brain activity became more chaotic and less predictable -- the opposite to what is seen in states of reduced consciousness, such as in deep sleep or under general anaesthesia.

"The changes in brain activity that accompany DMT are slightly different from what we see with other psychedelics, such as psilocybin or LSD, where we see mainly only reductions in brainwaves," said lead author Christopher Timmermann, from the Centre for Psychedelic Research.

"Here we saw an emergent rhythm that was present during the most intense part of the experience, suggesting an emerging order amidst the otherwise chaotic patterns of brain activity. From the altered brainwaves and participants' reports, it's clear these people are completely immersed in their experience -- it's like daydreaming only far more vivid and immersive, it's like dreaming but with your eyes open."

Mr Timmermann explains that while it's unclear as to whether DMT may have any clinical potential at this stage, the group hopes to take the work further by delivering a continuous infusion of DMT to extend the window of the psychedelic experience and collect more data.

The team says future studies could include more sophisticated measurements of brain activity, such as fMRI, to show which regions and networks of the brain are affected by DMT. They believe the visual cortex, the large area towards the back of the brain, is likely to be involved.

Dr Robin Carhart-Harris, head of Centre for Psychedelic Research, said: "DMT is a particularly intriguing psychedelic. The visual vividness and depth of immersion produced by high-doses of the substance seems to be on a scale above what is reported with more widely studied psychedelics such as psilocybin or 'magic mushrooms'.

"It's hard to capture and communicate what it is like for people experiencing DMT but likening it to dreaming while awake or a near-death experience is useful.

"Our sense it that research with DMT may yield important insights into the relationship between brain activity and consciousness, and this small study is a first step along that road."

https://www.sciencedaily.com/releases/2019/11/191119075305.htm

Psychedelic microdosing in rats shows beneficial effects

March 4, 2019

Science Daily/University of California - Davis

Microdosing -- taking tiny amounts of psychedelic drugs to boost mood and mental acuity -- is based on anecdotal reports of its benefits. Now, a study in rats suggests microdosing can provide relief for symptoms of depression and anxiety, but also has potential negative effects.

The growing popularity of microdosing -- taking tiny amounts of psychedelic drugs to boost mood and mental acuity -- is based on anecdotal reports of its benefits. Now, a study in rats by researchers at the University of California, Davis suggests microdosing can provide relief for symptoms of depression and anxiety, but also found potential negative effects. The work is published March 4 in the journal ACS Chemical Neuroscience.

"Prior to our study, essentially nothing was known about the effects of psychedelic microdosing on animal behaviors," said David Olson, assistant professor in the UC Davis departments of Chemistry and of Biochemistry and Molecular Medicine, who leads the research team. "This is the first time anyone has demonstrated in animals that psychedelic microdosing might actually have some beneficial effects, particularly for depression or anxiety. It's exciting, but the potentially adverse changes in neuronal structure and metabolism that we observe emphasize the need for additional studies."

Testing microdosing claims

Olson's group microdosed male and female rats with DMT, short for N,N-dimethyltryptamine. A psychedelic compound found in ayahuasca tea, DMT's molecular structure is embedded within the structures of popular microdosing drugs such as LSD and psilocybin. The researchers administered one-tenth of the estimated hallucinogenic dose in rats (1 milligram per kilogram of body weight) every third day for two months. Although there is no well-established definition of what constitutes a microdose, people who microdose tend to follow a similar schedule, taking one-tenth of a "trip" dose every three days. The rats were treated for two weeks before beginning behavioral tests relevant to mood, anxiety and cognitive function, and tests were completed during the two-day period between doses.

Olson's group found DMT microdosing helped rats to overcome a "fear response" in a test considered to be a model of anxiety and post-traumatic stress disorder (PTSD) in humans. The researchers also documented reduced immobility in an experiment that measures the effectiveness of antidepressant compounds. Less immobility is associated with antidepressant effects. In tests of cognitive function and sociability, the UC Davis researchers did not find any obvious impairments or improvements, which contrasts with human anecdotal reports.

Microdosing: potential risks

The team documented some potential risks: the dosing regimen significantly increased bodyweight in male rats, for example. It also caused neuronal atrophy in female rats. The latter change was unexpected, as previously Olson's group reported that rats treated with a single high dose of DMT showed increased neuronal growth. The results suggest an acute hallucinogenic dose and chronic, intermittent low doses of DMT produce very different biochemical and structural phenotypes, Olson said.

Despite the potential adverse effects of microdosing, the findings mean that it's possible to decouple the hallucinogenic effects from the therapeutic properties of these compounds.

"Our study demonstrates that psychedelics can produce beneficial behavioral effects without drastically altering perception, which is a critical step towards producing viable medicines inspired by these compounds," Olson said.

https://www.sciencedaily.com/releases/2019/03/190304100015.htm

Traditional Amazonian drug linked to improved sense of wellbeing

November 9, 2017

Science Daily/University of Exeter

A psychedelic drug traditionally used in South America improves people's general sense of wellbeing and may offer a treatment for alcoholism and depression, new research suggests.

Ayahuasca, a psychedelic brew often used in the Amazon region, contains dimethyltryptamine (DMT) -- an illegal class A drug in the UK.

Previous research has suggested that psychedelic drugs such as LSD and magic mushrooms can help alcoholics tackle their addiction.

Using Global Drug Survey data from more than 96,000 people worldwide, researchers from the University of Exeter and University College London found that ayahuasca users reported lower problematic alcohol use than people who took LSD or magic mushrooms.

Ayahuasca users also reported higher general wellbeing over the previous 12 months than other respondents in the survey.

"These findings lend some support to the notion that ayahuasca could be an important and powerful tool in treating depression and alcohol use disorders," said lead author Dr Will Lawn, of University College London.

"Recent research has demonstrated ayahuasca's potential as a psychiatric medicine, and our current study provides further evidence that it may be a safe and promising treatment.

"It is important to note that these data are purely observational and do not demonstrate causality.

"Moreover, ayahuasca users in this survey still had an average drinking level which would be considered hazardous. Therefore, randomised controlled trials must be carried out to fully examine ayahuasca's ability to help treat mood and addiction disorders.

"However, this study is notable because it is, to the best of our knowledge, the largest survey of ayahuasca users completed to date."

Ayahuasca -- a blend of the Psychotria Viridis bush and the stems of the Banisteriopsis Caapi vine -- is used by indigenous tribes and religious groups in the Amazon region, as well as many visitors.

The online survey, which was promoted via social media, measured wellbeing using the Personal Wellbeing Index -- a tool used by researchers around the world which asks about things such as personal relationships, connection with the community and a sense of achievement.

Of the respondents, 527 were ayahuasca users, 18,138 used LSD or magic mushrooms and 78,236 did not take psychedelic drugs.

Senior author Professor Celia Morgan, of the University of Exeter, said: "If ayahuasca is to represent an important treatment, it is critical that its short and long-term effects are investigated, and safety established.

"Several observational studies have examined the long-term effects of regular ayahuasca use in the religious context.

"In this work, long-term ayahuasca use has not been found to impact on cognitive ability, produce addiction or worsen mental health problems.

"In fact, some of these observational studies suggest that ayahuasca use is associated with less problematic alcohol and drug use, and better mental health and cognitive functioning."

However, the survey data showed a higher incidence of lifetime mental illness diagnoses within the ayahuasca users. Subsequent analyses found that these were confined to users from countries without a tradition of ayahuasca use.

The researchers said future studies should examine the relationships between ayahuasca use, mental health, wellbeing and problematic alcohol and substance use among these people.

The survey also asked people about the experiences of ayahuasca, and most users said they took the drug with a healer or a shaman.

Ayahuasca was rated as less pleasant and with less of an urge to use more of it than LSD or magic mushrooms. Its acute effects usually lasted for six hours, and were most strongly felt one hour after consumption.

The paper, published in the Nature journal Scientific Reports, is entitled: "Well-being, problematic alcohol consumption and acute subjective drug effects in past-year ayahuasca users: a large, international, self-selecting online survey."

https://www.sciencedaily.com/releases/2017/11/171109093134.htm

Substance present in ayahuasca brew stimulates generation of human neural cells

Harmine increases the number of neural progenitors, cells that give rise to neurons, study suggests

December 7, 2016

Science Daily/D'Or Institute for Research and Education

Human neural progenitors exposed to harmine, an alkaloid presented at the psychotropic plant decoction ayahuasca, led to a 70 percent increase in proliferation of these cells. The effect of generating new human neural cells involves the inhibition of DYRK1A, a gene that is over activated in patients with Down syndrome and Alzheimer's Disease. Thus harmine could have a potential neurogenesis role and possibly a therapeutic one over cognitive deficits.

Ayahuasca is a beverage that has been used for centuries by Native South-Americans. Studies suggest that it exhibits anxiolytic and antidepressant effects in humans. One of the main substances present in the beverage is harmine, a beta-carboline which potential therapeutic effects for depression has been recently described in mice.

"It has been shown in rodents that antidepressant medication acts by inducing neurogenesis. So we decided to test if harmine, an alkaloid with the highest concentration in the psychotropic plant decoction ayahuasca, would trigger neurogenesis in human neural cells," said Vanja Dakic, PhD student and one of the authors in the study.

In order to elucidate these effects, researchers from the D'Or Institute for Research and Education (IDOR) and the Institute of Biomedical Sciences at the Federal University of Rio de Janeiro (ICB-UFRJ) exposed human neural progenitors to this beta-carboline. After four days, harmine led to a 70% increase in proliferation of human neural progenitor cells.

Researchers were also able to identify how the human neural cells respond to harmine. The described effect involves the inhibition of DYRK1A, which is located on chromosome 21 and is over activated in patients with Down syndrome and Alzheimer's Disease.

"Our results demonstrate that harmine is able to generate new human neural cells, similarly to the effects of classical antidepressant drugs, which frequently are followed by diverse side effects. Moreover, the observation that harmine inhibits DYRK1A in neural cells allows us to speculate about future studies to test its potential therapeutic role over cognitive deficits observed in Down syndrome and neurodegenerative diseases," suggests Stevens Rehen, researcher from IDOR and ICB-UFRJ.

https://www.sciencedaily.com/releases/2016/12/161207124115.htm