Psychedelics Promote Neural Plasticity
A new study from the University of California, Davis has found that psychedelic drugs such as LSD and DMT promote neural plasticity and development, indicating a potential mechanism for their therapeutic benefits.
Patients who suffer from depression and post-traumatic-stress-disorder tend to have impaired neurogenesis and neuroplasticity – their brain cells grow more slowly and are less adaptable. These structural changes can lead to atrophy of various brain regions, including the hippocampus (which is involved in learning and memory) and the prefrontal cortex (which mediates personality and decision-making).
Counteracting this damage by promoting structural and functional neural plasticity has been suggested as novel way of treating psychiatric disorders. However, relatively few compounds that promote neuroplasticity – which the authors of the new study term ‘psychoplastogens’ – have been found capable of achieving this without drawbacks.
Ketamine, a dissociative anaesthetic with hallucinogenic properties, is a notable exception. By activating pathways involved with forming neurone connections, it has been found to be an extremely effective therapeutic for treatment-resistant depression (figure 1b).
Similarly, the Beckley/Imperial Psychedelic Research Programme have demonstrated significant and even longer-lasting benefits of psilocybin in the treatment of depression (figure 1a).
This new study hoped to elucidate the cellular mechanism by which psychedelics achieve their therapeutic effect by investigating whether and how they affect neural growth and plasticity.
In the first experiment, scientists treated cultures of cortical neurones with psychedelics, and then observed how the neurones developed and increased in complexity (figure 2).
They found that LSD, DMT, and DOI – all serotonergic psychedelics – significantly increased the growth and complexity of neurones in a similar manner to ketamine, with LSD particularly potent. Interestingly, ibogaine was found to have no effect on neuroplasticity – but its metabolite noribogaine did, suggesting it was the active molecule in the anti-addictive properties of iboga.
As a comparison, amphetamine and serotonin – which share structural similarities with psychedelics – were also tested, and were found to have no effect on measures of neurogenesis.
These effects were observed not only in cell cultures, but also by testing the compounds on the brains of fly larvae and zebrafish, showing that they also have a tangible effect in living organisms.
In a separate measure of neural plasticity, psychedelics were found to significantly increase the number of dendritic spines on cortical neurones, with LSD almost doubling their density (figure 3). These spines form synapses with other neurones and are a major site of molecular activity in the brain. Their functioning is closely related to higher cognition, and loss of these structures is a hallmark of depression and other neuropsychiatric disorders.
The positive effects were not only structural, but functional – electrophysiological recordings found that the frequency and strength of neural currents were increased for many hours after the psychedelic compounds had been removed.
The study then further elucidated the molecular mechanisms involved. mTOR is a key component of internal neural signalling pathways, involved with recruiting receptors and forming synapses, and is also known to be the target through which ketamine achieves its antidepressant effect. When mTOR was blocked, the psychoplastogenic effects of psychedelics seen above were also inhibited, indicating that they achieve their effect through a similar mechanism to ketamine.
This study builds on previous findings by the Beckley/Sant Pau Research Programme, which observed that components of the psychedelic brew ayahuasca promoted growth and maturation of neurones (figure 4). Ayahuasca has also been demonstrated to have significant anti-depressant effects, further suggesting neuroplasticity as a common mechanism for the actions of ketamine and psychedelics like LSD and ayahuasca. The Beckley Foundation is determined to investigate this further, both in vitro and in humans, as part of our Research Programmes with Brazil, Maastricht University and Imperial College London.
These findings add yet more scientific evidence for the therapeutic benefit of psychedelic compounds. Not only have psychedelics been demonstrated to have ground-breaking potential in treating previously untreatable psychiatric disorders, but they are almost unique in their ability to promote neuroplasticity in a safe way, healing both mind and brain.
Sadly, psilocybin, LSD, DMT, and other psychedelics remain on Schedule I of both the UK and the UN’s global drug conventions, severely limiting both research and clinical application. The Beckley Foundation is actively campaigning to have psychedelics and other psychoactive medicines re-scheduled, so that doctors and psychotherapists may use them as a tool to help heal those who are not benefiting from currently available treatments. Despite restrictions, we continue to collaborate with research groups all over the world to better understand these compounds – together, we hope to create a paradigm shift in psychiatry which will benefit all of society.