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Greaves, M. D.

Publications and source records attributed to Greaves, M. D..

3 recordsLinked to original sources

PsiConnect: A Multimodal Neuroimaging Study of Psilocybin-Induced Changes in Brain and Behaviour

PsiConnect is a large-scale neuroimaging study designed to investigate the neural and subjective effects of psilocybin using multimodal neuroimaging. It combines functional, structural, and diffusion-weighted MRI with EEG to examine brain activity in 62 participants before and after a 19 mg dose of psilocybin. The design includes resting-state scans and three naturalistic conditions: guided meditation, music listening, and movie watching. Half of the cohort underwent an 8-week meditation training program, enabling the exploration of interactions among meditation, psilocybin, and brain function. The fMRI data was obtained through multi-echo fMRI, which enhances the signal-to-noise ratio and reduces susceptibility artifacts, thereby improving the reliability of the analyses. A comprehensive battery of behavioural and self-report measures captured both acute and longitudinal cognitive and subjective effects, with follow-ups extending to one year post-administration. The large sample size, multimodal neuroimaging, diversity of contexts, and longitudinal behavioural follow-ups enable the study of psilocybin-induced changes in brain and behaviour with an unprecedented level of detail and reliability. Furthermore, the data is curated according to open science principles to ensure accessibility and interoperability with established neuroimaging processing pipelines. These factors make PsiConnect a valuable and highly reusable resource for researchers in cognitive and computational neuroscience.

neuroscience↗

Psychedelics Align Brain Activity with Context

Psychedelics can profoundly alter consciousness by reorganising brain connectivity; however, their effects are context-sensitive. To understand how this reorganisation depends on context, we collected and comprehensively analysed the largest psychedelic neuroimaging dataset to date. Sixty-two adults were scanned with functional MRI and EEG during rest and naturalistic stimuli (meditation, music, and movie), before and after ingesting 19 mg of psilocybin (functional MRI {approx}80 min post-dose; EEG {approx}150 min post-dose). Half the participants ranked the experience among the most meaningful of their lives. Under psilocybin, functional MRI and EEG signals recorded during eyes-closed conditions became similar to those recorded during an eyes-open condition. Global functional connectivity increased in associative regions and decreased in sensory areas. Using machine learning to represent neural activity as low-dimensional trajectories, we found that psilocybin reorganised these into structured, context-sensitive patterns of brain activity that reflected both experimental condition and the quality of subjective experience, revealing an organisation that was missed by time-averaged connectivity measures. Under psilocybin, brain networks that ordinarily segregate internal and external processing coherently integrated and aligned neural dynamics with context. This context-alignment manifested as distinct and cohesive neural trajectories in participants reporting positively felt self- and boundary-dissolving effects, corresponding to the felt experience of being part of the environment, which we refer to as embeddedness--the subjective experience of being continuous with, rather than separate from, the surrounding environment. The strength of this context-alignment was associated with next-day mindset change, bridging the neural, experiential, and therapeutic dimensions of the psychedelic state. These findings show that the organisation of brain activity covaries with the experiential coherence of the psychedelic state, and provide a systems-level framework for how context-sensitive brain dynamics link neurobiology to subjective experience and behavioural change.

neuroscience↗

Structurally informed resting-state effective connectivity recapitulates cortical hierarchy

Neuronal communication relies on the anatomy of the brain, yet it remains unclear whether, at the macroscale, structural (or anatomical) connectivity provides useful constraints for modeling effective connectivity. Here, we assess a hierarchical empirical Bayes model that builds on a well-established dynamic causal model by integrating structural connectivity into resting-state effective connectivity via priors. In silico analyses show that the model successfully recovers ground-truth effective connectivity and compares favorably with a popular alternative. Analyses of empirical data reveal that a positive, monotonic relationship between structural connectivity and the prior variance of group-level effective connectivity generalizes across sessions and samples. Finally, attesting to the models biological plausibility, we show that inter-network differences in the coupling between structural and effective connectivity recapitulate a well-known unimodal- transmodal hierarchy. These findings underscore the value of integrating structural and effective connectivity to enhance understanding of functional integration, with implications for health and disease. Significance statementTo advance the understanding of how neuronal populations interact in vivo, it is essential to develop models that integrate neuroimaging modalities. Here, we show that integrating structural connectivity into dynamic causal modeling of resting-state effective connectivity substantially improves model evidence, yields reliable inferences, and demonstrates face and construct validity in silico. Furthermore, this integration reveals that structural connectivitys influence on effective connectivity varies along an established unimodal-transmodal cortical hierarchy. This finding provides the first evidence of a network-dependent modulation of the relationship between structural and effective connectivity in humans. Against the backdrop of sustained and widespread interest in dynamic causal modeling, this study highlights the added value of integrating structural connectivity-based constraints, offering a more biologically grounded account of brain dynamics.

neuroscience↗