4.7 Article

Serotonergic psychedelic drugs LSD and psilocybin reduce the hierarchical differentiation of unimodal and transmodal cortex

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NEUROIMAGE
卷 256, 期 -, 页码 -

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ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2022.119220

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资金

  1. National Sciences and Engineering Research Council of Canada (NSERC) [WANDERINGMINDS-646927]
  2. National Sciences and Engineering Research Council of Canada (NSERC) [FDN-154298]
  3. Alexander Graham Bell Canada Graduate Scholarships, CGS-D
  4. European Research Council Consolidator award [WANDERINGMINDS-646927]
  5. Canadian Institutes of Health Research (CIHR) [1304413]
  6. Canada Research Chairs program (CRC-Tier 2 in Cognitive Neuroinformatics of Healthy and Diseased Brains)
  7. Alex Mosley Charitable Trust
  8. center for Psychedelic Research
  9. Beckley Foundation, Beckley-Imperial Research Programme

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LSD and psilocybin, two serotonergic psychedelic compounds, have potential therapeutic applications for mental health disorders. Neuroimaging studies have shown that these compounds can alter whole-brain functional organization and dynamics. A recent study proposed a model suggesting reduced hierarchical organization as a key mechanism underlying the psychedelic state, and our analysis supported this hypothesis. We found that the principal gradient of cortical connectivity, representing a hierarchy from unimodal to transmodal cortex, was flattened under both drugs. This was driven by a reduction of functional differentiation at both hierarchical extremes and an increase in unimodal-transmodal crosstalk.
Lysergic acid diethylamide (LSD) and psilocybin are serotonergic psychedelic compounds with potential in the treatment of mental health disorders. Past neuroimaging investigations have revealed that both compounds can elicit significant changes to whole-brain functional organization and dynamics. A recent proposal linked past findings into a unified model and hypothesized reduced whole-brain hierarchical organization as a key mechanism underlying the psychedelic state, but this has yet to be directly tested. We applied a non-linear dimensionality reduction technique previously used to map hierarchical connectivity gradients to assess cortical organization in the LSD and psilocybin state from two previously published pharmacological resting-state fMRI datasets ( N = 15 and 9, respectively). Results supported our primary hypothesis: The principal gradient of cortical connectivity, describing a hierarchy from unimodal to transmodal cortex, was significantly flattened under both drugs relative to their respective placebo conditions. Between-condition contrasts revealed that this was driven by a reduction of functional differentiation at both hierarchical extremes - default and frontoparietal networks at the upper end, and somatomotor at the lower. Gradient-based connectivity mapping indicated that this was underpinned by a disruption of modular unimodal connectivity and increased unimodal-transmodal crosstalk. Results involving the second and third gradient, which, respectively represent axes of sensory and executive differentiation, also showed significant alterations across both drugs. These findings provide support for a recent mechanistic model of the psychedelic state relevant to therapeutic applications of psychedelics. More fundamentally, we provide the first evidence that macroscale connectivity gradients are sensitive to an acute pharmacological manipulation, supporting a role for psychedelics as scientific tools to perturb cortical functional organization.

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