Author:
Whelan Tobias P.,Daly Eileen,Puts Nicolaas A.,Smith Paula,Allison Carrie,Baron-Cohen Simon,Malievskaia Ekaterina,Murphy Declan G. M.,McAlonan Grainne M.
Abstract
Abstract
Background
The underlying neurobiology of the complex autism phenotype remains obscure, although accumulating evidence implicates the serotonin system and especially the 5HT2A receptor. However, previous research has largely relied upon association or correlation studies to link differences in serotonin targets to autism. To directly establish that serotonergic signalling is involved in a candidate brain function our approach is to change it and observe a shift in that function.
We will use psilocybin as a pharmacological probe of the serotonin system in vivo. We will directly test the hypothesis that serotonergic targets of psilocybin – principally, but not exclusively, 5HT2A receptor pathways—function differently in autistic and non-autistic adults.
Methods
The ‘PSILAUT’ “shiftability” study is a case–control study autistic and non-autistic adults. How neural responses ‘shift’ in response to low doses (2 mg and 5 mg) of psilocybin compared to placebo will be examined using multimodal techniques including functional MRI and EEG. Each participant will attend on up to three separate visits with drug or placebo administration in a double-blind and randomized order.
Results
This study will provide the first direct evidence that the serotonin targets of psilocybin function differently in the autistic and non-autistic brain. We will also examine individual differences in serotonin system function.
Conclusions
This work will inform our understanding of the neurobiology of autism as well as decisions about future clinical trials of psilocybin and/or related compounds including stratification approaches.
Trial registration
NCT05651126.
Publisher
Springer Science and Business Media LLC