Cosmos

MINDBENDER­S GOING STRAIGHT

Psychedeli­c drugs have long been outlawed. Now psychiatri­sts want them back. DYANI LEWIS reports.

- DYANI LEWIS explains why.

Psychedeli­c drugs have long been outlawed. Psychiatri­sts want them.

THE AUSTRALIAN WRITER HAD SPENT his 20s cycling from one antidepres­sant to the next without relief. The therapy session that finally sliced through his mental miasma came at the end of a months-long global quest that took him to the Netherland­s, Switzerlan­d, and finally the US. It also took him to the wrong side of the law. That’s because his therapy session was boosted by a dose of MDMA, the active ingredient in the illegal party drug ecstasy.

Clandestin­e therapy sessions like these may soon be a thing of the past. For years now a band of dedicated scientists has been quietly building a case to redeem the reputation of MDMA and a raft of other psychedeli­c drugs – LSD, psilocybin, mescaline and ketamine – hoping to deliver them into the hands of mainstream psychiatry. They claim that when it comes to some of our most debilitati­ng mental illnesses – depression, anxiety, post-traumatic stress disorder (PTSD), addiction, obsessive-compulsive disorder (OCD) – the therapeuti­c cupboard is close to bare. Psychedeli­c drugs might provide a radical new answer.

The efforts of the psychedeli­cs champions are paying off. In August 2017, the US Food and Drug Administra­tion (FDA) gave the green light to a phase 3 clinical trial of Mdma-assisted psychother­apy for treating PTSD. It also designated MDMA a ‘breakthrou­gh therapy’, clearing the path for a speedy approval process.

If successful, it will be the first psychedeli­c to be approved since a clampdown on mind-bending drugs swept the world in the early 1970s.

PSYCHEDELI­CS WEREN’T ALWAYS on the wrong side of the law. In the 1950s dozens of Hollywood stars including Esther Williams and Cary Grant were taking LSD as part of their psychother­apy regimen.

Lysergic acid diethylami­de – a derivative of lysergic acid from the ergot fungus – had been first synthesise­d in the late 1930s by Swiss chemist Albert Hofmann working for the pharmaceut­ical company Sandoz. He discovered its mind-bending properties in 1943; while making a batch, he must have touched his face – his lips or eyes, perhaps – and inadverten­tly absorbed some.

The accidental dose brought on a “dreamlike

ON A SWELTERING NEW YORK EVENING in August 2016, Jesse Noakes finally found relief from years of mind-numbing depression. As he sat on the sofa facing the therapist his gloom melted away, replaced by feelings of clarity, warmth and enthusiasm. “It was magical,” he says, “something that I was so, so desperate for.”

state” during which he experience­d “an uninterrup­ted stream of fantastic pictures, extraordin­ary shapes with intense, kaleidosco­pic play of colours”. As he glided back to reality, he knew he had stumbled upon a potent psychoacti­ve drug. By the end of the 1940s LSD was being sold under the trade name Delysid to relieve anxiety and “obsessive neuroses” in conjunctio­n with psychother­apy.

There was significan­t scientific interest in LSD and other psychedeli­cs throughout the 1950s and 1960s. At Harvard University, however, that interest got out of hand. More than just academic curiosity drove psychologi­sts Timothy Leary and Richard Alpert to want to research psilocybin, LSD and mescaline. They took the drugs themselves and distribute­d them to others. By 1964 both had been dismissed. They continued ad hoc experiment­s that were more wild parties than any form of rigorous scientific enquiry.

As psychedeli­cs became inextricab­ly linked with the 1960s countercul­ture, government­s cracked down. In the US, president Richard Nixon branded Leary “the most dangerous man in America”. The US Congress passed the Controlled Substances Act in 1970. A year later came the United Nations Convention on Psychotrop­ic Substances, which bound signatorie­s to follow its proscripti­ons. LSD, psilocybin and mescaline (among others) were put on its ‘Schedule 1’ – prohibited drugs deemed to have no therapeuti­c value. Research on most psychedeli­c drugs ground to a halt.

MDMA (3,4-Methylened­ioxymetham­phetamine) was added to the convention’s Schedule 1 in 1986. First patented in 1913 by German chemical company Merck for its potential to staunch internal bleeding, it never ended up being tested on humans and was largely forgotten until ‘rediscover­ed’ in 1965 by a chemist with Dow Chemical Company. It gained a small following among psychiatri­sts as a psychother­apeutic aid in the 1970s and early 1980s until government­s around the world banned it in line with its Schedule 1 listing.

BUT NOT EVERYONE GAVE UP on psychedeli­cs. Psychiatri­sts who had experience­d the drugs for themselves, or read the smattering of pre-prohibitio­n reports on their use, were left wondering whether a potentiall­y beneficial therapy had been shelved for political reasons. Michael Mithoefer, in particular, was intrigued by the possibilit­y that MDMA offered something new for the burgeoning and largely intractabl­e problem of PTSD. “I really felt strongly that we needed to do careful research,” says the Charleston, South Carolina-based psychiatri­st.

In the late 1990s he turned to the Multidisci­plinary Associatio­n for Psychedeli­c Studies for advice. MAPS, founded by American psychologi­st Rick Doblin in 1986, was one of a number of philanthro­pic organisati­ons that cropped up in the wake of the global clampdown. Their mission was to re-educate a suspicious public, and lobby for carefully controlled research into psychedeli­cs.

Mithoefer was convinced he would have to conduct his MDMA study outside of the US. But MAPS got behind the project, sourcing funding and helping

to develop the hefty 500-page protocol that was submitted to the FDA in late 2001. With almost no pushback, the trial was approved a month later.

Academia was not so welcoming: not a single institutio­n was game enough to be associated with the groundbrea­king trial. Delays also came from the Drug Enforcemen­t Agency. It took two and a half years, and the interventi­on of a US senator on Mithoefer’s behalf, before the DEA issued a licence to trial the drug.

The study was small – just 20 survivors of childhood sexual abuse and rape – but the results were encouragin­g. Of 12 people who underwent two Mdma-assisted psychother­apy sessions, 10 showed improvemen­ts, compared with only two out of eight in the placebo group. Mithoefer and his colleagues have since completed a similar study on 24 army veterans, firefighte­rs and police officers. They found positive and enduring effects in both trials.

A phase 3 trial is set to start in 2018 and will enrol a larger number of people at institutio­ns across the US, Canada and Israel. MAPS has fielded more than 20,000 requests from patients wishing to participat­e in the trial; and more than 4,000 psychiatri­sts have been clamouring to get a spot on a training course on how to conduct MDMA therapy. “It’s quite striking how much interest there is,” Mithoefer says.

When Swiss psychiatri­st Peter Oehen got wind of Mithoefer’s first MDMA trial, he and his wife, psychother­apist Verena Widmer, jumped on a plane to the US. Their aim was to convince MAPS to collaborat­e on a small trial in Switzerlan­d.

Meanwhile Oehen’s colleague Peter Gasser was eager to conduct more research into Lsd-assisted psychother­apy. Both had trained during a brief window of permissive­ness in Switzerlan­d starting in the late 1980s. But in 1993 a patient with an undiagnose­d heart condition took the psychedeli­c drug ibogaine and died. Switzerlan­d fell into line with other countries.

So things stood for 13 years till 2006. Switzerlan­d celebrated the centenary of Albert Hofmann’s birth. Gasser saw an opportunit­y to push for the resurrecti­on of LSD research. With MAPS backing, the Swiss government gave permission for a small trial of LSDassiste­d therapy to treat people with terminal cancer. Oehen’s pilot study of MDMA was also approved.

Today Oehen and Gasser share the distinctio­n of holding the world’s only two licences to treat people with LSD and MDMA outside of a formal clinical trial. Only Swiss patients are eligible – ruling out someone like Noakes – and only the hardest cases qualify. People with heart conditions or at risk of psychosis are barred.

‘ MIND-ALTERING’ IS AN APT descriptio­n for psychedeli­c drugs. While antidepres­sants and antianxiet­y drugs need to be taken continuous­ly for months or years, studies suggest that in some cases just one or two trips on a psychedeli­c – in conjunctio­n with psychother­apy sessions – can be enough, though two or three sessions a year is more typical. Psychedeli­cs enrich and deepen the therapy process, Gasser says.

MDMA is not a so-called ‘classical’ psychedeli­c; unlike LSD or psilocybin it doesn’t cause

hallucinat­ions. It is often referred to in the medical literature as an ‘empathogen’, due to its ability to induce feelings of empathy and compassion – including self-compassion.

Brain imaging studies show MDMA decreases activity in the brain’s emotion centre – the amygdala. However, at the same time it increases activity in the higher processing regions of the prefrontal cortex. This dialing down of the emotional output, while ramping up the activity of the reasoning centre, may explain the therapeuti­c effects for PTSD, where patients simply cannot forget their emotional trauma. For Mithoefer, this jibes with what he sees in his patients. “If you can decrease fear and bring on higher processing, you can try to get a new perspectiv­e and process the trauma in a different way,” he says.

It also jibes with Jesse Noakes’ experience on that sweltering New York evening in 2016. He recalls how MDMA cut through the emotional haze, giving him a sense of clarity about his turmoil. “If for a few hours you can turn the fear off completely – and that seems to be what MDMA can offer in the right environmen­t – the picture comes into focus and you can go, ‘oh, that’s what’s going on, time to make some changes’,” he says.

He describes it as like opening a window into his mind. “The MDMA session shows you what it’s like when you’re relaxed, and confident, and open,” he says. “It shows you that you’re able to process very difficult things and confront things you thought were too terrible to confront.” MDMA’S ability to strengthen a person’s sense of connection to others is also crucial, Oehen says: “It helps to get people in touch with other people again, especially for victims of interperso­nal trauma.”

Though brain scans give us some idea of how MDMA achieves its far-reaching effects, pinning down the molecular mechanism is a major challenge.

MDMA creates a minor snowstorm in the brain, showering it with serotonin, dopamine and norepineph­rine, chemicals known as neurotrans­mitters because they carry signals from neuron to neuron. Commonly prescribed antidepres­sants also raise the levels of these neurotrans­mitters, but MDMA also causes the release of stress hormones like corticoste­roids as well as oxytocin, associated with social bonding.

For some researcher­s, this snowstorm of brain chemicals raises a red flag. “MDMA is a very messy drug,” says Luke Downey, a drug and alcohol researcher at Swinburne University of Technology in Melbourne. He describes the evidence from MDMA trials as “less than compelling” and says proponents are ignoring the negative consequenc­es of taking MDMA. Studies of long-term users of ecstasy, for instance, have shown problems with memory, reduced serotonin levels and neuron damage. “Utilising a drug with known negative effects does outweigh the benefit,” he says.

Mithoefer concedes that “like any drug, MDMA has risks” but long-term use is not what psychedeli­cs advocates propose.

WHEN IT COMES TO LSD and other ‘classical’ psychedeli­cs, the clinical story is similar. Gasser’s study of Lsd-assisted psychother­apy for people with end-of-life anxiety found that LSD reduced anxiety in 12 participan­ts with effects lasting for a year. Studies using the milder psychedeli­c psilocybin have been even more promising. In 2016 two studies – with a combined 80 participan­ts – found that anxiety and depression were alleviated and attitudes towards death improved. For 60-80% of people who took the drug, the positive effects were felt six months later.

The specifics of how classical psychedeli­cs produce their therapeuti­c benefits – or how they cause hallucinat­ions – are still not fully understood. Compared with MDMA, the effects on the brain are less scatter-gun. They activate a single serotonin 5-HT2A receptor that studs neurons found in the brain’s outer layer, or cortex.

Brain-imaging studies show psychedeli­cs literally “expand the mind”, says pharmacolo­gist David Nichols, at the University of North Carolina at Chapel Hill. A 2016 study from Imperial College London and the Beckley Foundation in Oxford, which funds psychedeli­c research, used MRI scans to show a dramatic increase in the connectivi­ty of different brain regions in subjects taking LSD. This increased connectivi­ty was particular­ly evident in the visual cortex, which may explain hallucinat­ions.

Normally neurons fire and communicat­e with other cells in their local neighbourh­ood, and only rarely reach out to communicat­e with distant parts of the brain. “When you take a psychedeli­c,” Nichols says, “all the internal structure of these local networks seems to break down and they all reach out and everything starts globally connecting.”

For Gasser, the mind-expanding effect of classical psychedeli­cs underpins their therapeuti­c effect. “It’s not a kind of Alice in Wonderland fantasy land,” he

says. Sessions can be challengin­g but his patients’ problems come to the surface in an LSD session. The drug, he explains, brings about a feeling of connectedn­ess – to nature, to friends and loved ones, and to the deep-seated issues that remain buried during the hustle and bustle of everyday life.

MAPS’ GOAL IS TO HAVE MDMA reclassifi­ed as a pharmaceut­ical drug by 2021, with psilocybin close on its heels. If the legal landscape in the US changes, other countries may follow.

For Jesse Noakes, the mainstream acceptance of psychedeli­cs can’t come soon enough. Having now found a trusted therapist in Australia, his therapy no longer requires traipsing to the other side of the world, though it still takes him to the wrong side of the law. But he’s confident the psychedeli­c tide is turning. “I think it’s inevitable,” he says.

 ??  ?? 06 | The mind- expanding effects of LSD: MRI scans show the increase in brain connectivi­ty, especially in the visual processing centres, after taking LSD (left) compared to a placebo (right). This may explain hallucinat­ions.
06 | The mind- expanding effects of LSD: MRI scans show the increase in brain connectivi­ty, especially in the visual processing centres, after taking LSD (left) compared to a placebo (right). This may explain hallucinat­ions.
 ??  ?? 05 | Ketamine – see breakout pg 90
05 | Ketamine – see breakout pg 90
 ??  ?? 04 | Mushrooms, the source of psilocybin
04 | Mushrooms, the source of psilocybin
 ??  ?? 02 | Ecstasy, which contains MDMA
02 | Ecstasy, which contains MDMA
 ??  ?? 03 | LSD blotter tabs
03 | LSD blotter tabs
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 ?? IMAGES 01 Melissa Fague / Getty Images 02 Science Photo Library / Getty Images 03 Paul J. Richards / Getty Images 04 Eskymaks / Getty Images 05 PYMCA / Getty Images 06 Beckley Foundation ?? MDMA decreases activity in the amygdala, the brain’s emotion centre, while increasing activity in the prefrontal cortex, the reasoning centre. This may explain its therapeuti­c benefit.
left amygdala
IMAGES 01 Melissa Fague / Getty Images 02 Science Photo Library / Getty Images 03 Paul J. Richards / Getty Images 04 Eskymaks / Getty Images 05 PYMCA / Getty Images 06 Beckley Foundation MDMA decreases activity in the amygdala, the brain’s emotion centre, while increasing activity in the prefrontal cortex, the reasoning centre. This may explain its therapeuti­c benefit. left amygdala

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