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Microdosing is the practice of regularly using low doses of psychedelic drugs. This relatively recent phenomenon was made popular through the anecdotal reports of young professionals from all walks of life, taking sub-hallucinogenic doses of psychedelics for a variety of reasons.
In spite of the reported popularity of this practice, few scientific studies have explored the pharmacological effects of microdosing. Existing studies tend to be large-scale survey studies exploring why people microdose and the subsequent effects they experience after regularly consuming low doses of psychedelics.
The study at hand is not indifferent, it describes microdosing practices, motivations and mental health among a sample of self-selected microdosers (n = 4050) and non-microdosers (n = 4653). What makes this study unique is the manner through which data was collected; a mobile phone application.
Study participants downloaded the Quantified Citizen application to their iPhones and were instructed to complete a total of 123 questions surrounding their mental health and microdosing practices. While many companies are developing similar applications, this study is one of the first to quantify and analyse data collected in this manner.
- Psilocybin was the most commonly reported microdosed substance, with 85% of participants using psilocybin compared to 11% using LSD.
- Mental health or substance use concerns were reported by 29% of respondents, with the most frequently endorsed being anxiety, depression, and PTSD. Microdosers were more likely to report a history of mental health concerns compared to those who do not microdose.
- The most widely endorsed motivation for microdosing was Enhancing Mindfulness, followed by Improving Mood, Enhancing Creativity and Enhancing Learning.
- Psilocybin users were more likely than LSD users to combine psilocybin with other substances in the process referred to as stacking, combing substances such as Lion’s Mane, niacin and chocolate with their psychedelic of choice.
Overall, the study found that among individuals reporting mental health concerns, microdosers exhibited lower levels of depression, anxiety, and stress. While limitations do exist, particularly surrounding the manner in which participants were selected, the large sample size highlights that microdosing is common practice with a variety of motivations.
If it’s really the microdose that is doing the heavy lifting, or the expectancy effects surrounding it do remain elusive. A self-blinded experiment earlier this year found that all those who microdosed (so also those taking a placebo) improved. A study that combines the strength of both these studies, blinding participants and the large sample size, could provide more insights in the future.
How psychedelics exert their effects on the brain remains somewhat of a mystery. Understanding these neurophysiological mechanisms is essential in order to advance the medicalization of psychedelics. Thanks to modern neuroimaging techniques, researchers are constantly discovering more and more about these potential mechanisms.
In the present study, researchers at Johns Hopkins assessed the effects of psilocybin-assisted therapy on a number of neurological variables in patients who are depressed. These variables include; cognitive flexibility (the ability to adapt our behaviour and thinking in response to the environment), neural flexibility and neurometabolite concentrations. As well as using fMRI to assess these variables, the researchers created predictive models using the data in order to gain a deeper understanding of the neurophysiological effects elicited by psilocybin.
- Psilocybin therapy was shown to increase cognitive and neural flexibility in patients with major depressive disorder.
- There was a lack of correlation between improvements in cognitive flexibility and improvements in depression, suggesting that cognitive flexibility may not be mechanistically related to the antidepressant effects of psilocybin therapy.
- One week after treatment glutamate and N-acetylaspartate levels were decreased in the anterior cingulate cortex (ACC) suggesting that a decrease in neural metabolism may increase neural flexibility although further research is needed to establish this link.
- Larger pre- to post-treatment increases in dynamics of functional activity (dFC) between the ACC and the posterior cingulate cortex (PCC) and greater baseline dFC of the ACC was associated with fewer improvements in cognitive flexibility.
Overall, these findings suggest a new relationship between cognitive and neural flexibility. Practical implications of such findings suggest that patients with lower baseline neural flexibility may be more likely to benefit from psychedelic therapy. Such findings provide us with further insight with regards to how psychedelics may exert their effects and help us to further develop treatment models using psychedelics.
The exact nature of mental health disorders remains speculative at best, with both physiological and psychological factors involved in the aetiology of these disorders. Psychedelics are helping to treat these disorders although the manner in which they act remains unknown. Psychedelics can cause people to have intense psychological experiences all while inducing structural changes in the brain by promoting neurophysiological mechanisms like neuroplasticity.
In the present study, researchers sought to understand the molecular mechanisms underlying cognitive impairment and executive dysfunction associated with alcohol use disorder (AUD). Based on previous research, the researchers hypothesized that deficits of mGluR2 receptors in the medial prefrontal cortex may underlie the behavioural changes seen in AUD and that these changes could be treated using psilocybin. To test their hypothesis, researchers treated AUD rats using psilocybin.
This is what they saw in the rodents:
- Using advanced genetic tools and pharmacologically validated rat models of AUD, the researchers provide evidence that a mGluR2 deficit is both necessary and sufficient for diminished cognitive flexibility and increased drug craving.
- Psilocybin administration was capable of restoring mGluR2 deficit in alcohol-dependent rats and thus could decrease relapse behaviour and may also positively impact cognitive flexibility.
- The authors describe a novel FDG-Positron Emission Tomogrpahy (PET) biomarker strategy to identify mGluR2 treatment responsive individuals. Such a technique may contribute to enhancing therapeutic outcomes in patients with AUD.
The findings of this study provide support for mGluR2 as a molecular target for treating reduced cognitive flexibility, craving, and relapse responses in alcohol-dependent patients. However, as this study was conducted using rodent models such findings may not translate to humans.
Clinical research is needed in order to determine this effect. Nonetheless, the findings support the use of psilocybin to treat AUD both psychologically, as previous research has suggested, and physiologically.
Research Report Readout
In a double-blind placebo-controlled trial, the effect of psilocybin (25mg) was assessed in healthy volunteers who had been taking the antidepressant escitalopram or placebo before psilocybin treatment. Pretreatment with escitalopram had no relevant effect on positive mood but significantly reduced bad drug effects, adverse cardiovascular effects, and other adverse effects of psilocybin compared with placebo pretreatment.
A longitudinal study assessed data from three ongoing open prospective cohorts of people who use drugs (PWUD) in Vancouver, Canada to investigate the relationship between psychedelic use and daily opioid use. This is the first study to find that recent psychedelic use was associated with 55% reduced odds of daily opioid use.
The link between serotonergic psychedelic’s and language production is explored. It is shown that language production can be used to predict the therapeutic outcomes of individual psychedelic experiences and therefore, brief interviews obtained before, during and after the experience may expand the range of potential scientific conclusions.
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