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Vohryzek, J.

Publications and source records attributed to Vohryzek, J..

At least 19 recordsLinked to original sources

Diminished ascending drive in transdiagnostic anhedonia shifts the cortico-subcortical hierarchy away from bottom-up dominance

Anhedonia, the diminished capacity to experience or pursue pleasure, is a core feature of mood and psychotic disorders, yet the large-scale brain dynamics underlying it remain uncharacterized. Dominant accounts posit striatal hypofunction with compensatory prefrontal over-recruitment, but they rest on activation magnitudes and symmetric correlations, which cannot resolve the direction of influence. Here, in 210 adults from the Transdiagnostic Connectome Project, we defined symptom-derived low- and high-anhedonia subgroups and estimated each participant's directed effective connectivity using a whole-brain generative model fitted to resting-state fMRI. In high anhedonia, the cortex shifted upstream relative to the subcortex, flattening the cortico-subcortical hierarchy. Correspondingly, the net balance of direct cortico-subcortical flow shifted from bottom-up to balanced. This shift recurred within the frontostriatal reward circuit and replicated across independent halves of each participant's data. Flow asymmetry also increased with subject-level severity. Decomposing flow into ascending and descending arms showed that both weakened in high anhedonia, but ascending subcortex-to-cortex and striatum-to-prefrontal drive fell more than the descending drive. These findings identify a reorganization of cortico-subcortical hierarchy in anhedonia and suggest that the previously reported prefrontal over-recruitment reflects diminished ascending drive rather than stronger cortical output.

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Whole-brain receptor markers and hub excitabilities determine acute and long-term outcomes in stroke

Following a stroke, changes in receptor systems have been observed that may influence the excitability of affected brain regions and drive recovery trajectories. Translating results from animal studies to patients remains a major challenge, and while imaging modalities have provided a wealth of findings, a mechanistic link between local receptor systems and observed imaging data is still missing. To bridge this gap, we built patient-specific digital twins with their own neuromodulatory profiles: we integrated 19 receptor and transporter density maps into a mechanistic whole-brain model, and estimated their influence on cortical excitability for each stroke patient and how these systems subsequently explain recovery trajectories. We found that distinct receptor profiles modulated excitability in perilesional versus non-perilesional tissue. Favourable acute motor outcomes were most strongly explained by increased inhibition mediated by non-perilesional GABA-A receptors, together with enhanced excitability driven by cannabinoid, histaminergic, and noradrenergic systems. For acute language outcomes, we identified receptor signatures that, together with motor findings, formed two cross-domain clusters linking excitability to either better or poorer performance. Remarkably, structurally highly connected hubs played a key role: their acute excitability explained cognitive and language deficits and predicted language recovery at one year. Together, our results establish a mechanistic link between receptor-specific modulation of cortical excitability and behavioural recovery, highlighting potential targets for pharmacological and non-invasive therapeutic interventions.

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Spiral brain dynamics track the temporal unfolding of subjective intensity during the N,N-dimethyltryptamine experience

Psychedelic compounds such as N,N-dimethyltryptamine (DMT) induce rapid and profound changes in conscious experience, requiring neuroimaging measures that capture how brain dynamics evolve across space and time. Emerging evidence suggests that rotational (vortex-like) dynamics may contribute to the coordination of large-scale neural activity. Here, we introduce two vorticity-based metrics; spiral vorticity (SV) and spatial spiral vorticity dispersion (SSVD), to quantify the rotational organization and spatial heterogeneity of large-scale cortical phase dynamics. Using fMRI data acquired under placebo and DMT in a within-subject design, we assessed these measures globally, across resting-state networks, and regionally to examine their relationship to subjective intensity. DMT increased SV and SSVD and reduced temporal irreversibility, indicating stronger rotational organization, greater spatial heterogeneity, and altered directional structure of cortical dynamics. Effects were non-uniform across functional systems, with the largest changes in default mode, visual, frontoparietal, and dorsal attention networks. Both vorticity measures tracked the temporal evolution of subjective intensity globally, while network-level analyses revealed spatially heterogeneous brain-experience coupling. Spatiotemporally resolved analyses further showed that the strongest reorganization of spiral dynamics emerged during offset and recovery rather than at peak subjective intensity. These findings identify spiral dynamics as a time-resolved neural signature of the DMT experience. By quantifying the rotational structure and spatial heterogeneity of cortical phase flow, vorticity-based measures provide a framework for linking large-scale brain dynamics to evolving subjective experience.

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Flattened brain hierarchy and increased EEG complexity during unusual bodily experiences and out-of-body experiences

Experiences in which the sense of the body becomes distorted offer a unique window into how the brain constructs the bodily self. Despite their clinical relevance in conditions such as depersonalization and body-image disorders, large-scale brain dynamics underlying unusual bodily experiences (UBEs) remain poorly understood, and no prior study has examined them systematically across wakefulness and sleep. Here, we analyzed a high-density EEG dataset including 36 UBE episodes, such as floating sensations, distorted body boundaries, and out-of-body experiences, recorded across rapid eye-movement (REM) sleep, light sleep, sleep arousals, and wakefulness during meditation (N=20). We quantified the temporal irreversibility of neural dynamics, a marker of cortical hierarchical organization, and complemented these analyses with whole-brain signal complexity measures following a within-subject design. UBEs were consistently associated with a global reduction in neural irreversibility and cortical hierarchical differentiation relative to non-UBEs and wakefulness, along with a concurrent increase in whole-brain complexity to levels comparable to wakefulness. Together, these findings suggest that UBEs reflect a neural state combining high informational richness with a transient flattening of cortical hierarchy, a profile that resembles that observed in psychedelic states. Key pointsO_LIUBEs are associated with a global flattening of brain hierarchy measured by EEG. C_LIO_LIUBEs are associated with increased global EEG complexity, resembling the psychedelic state. C_LI

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The blueprint of human functional architecture shifts from cognition to anatomy during perturbations of consciousness

Consciousness and cognition arise from the ongoing interactions between brain regions. Synchronous fluctuations of fMRI signals may indicate that two brain regions perform similar cognitive functions, but neural interactions are also constrained by anatomical connectivity and regions molecular, cytoarchitectonic, and metabolic profiles. Here we disentangle the respective contributions of ongoing cognition and multimodal neurobiological constraints in shaping functional connectivity. We jointly contextualise haemodynamic FC against eight distinct multimodal representations of the human connectome: (i) structural connectivity from diffusion tractography; (ii) spatial embedding; (iii) similarity of transcriptional profiles from gene expression; (iv) similarity of receptor profiles from Positron Emission Tomography; (v) laminar profile similarity from histology; (vi) correlated electrophysiological activity from magnetoencephalography; (vii) correlated metabolic activity from PET glucose uptake; (viii) coordinated activation across 123 cognitive operations from the NeuroSynth meta-analytic engine. We demonstrate that cognitive co-activation is the dominant predictor of inter-regional fMRI synchrony in the awake human brain, even when quantified using intracranial electrical stimulation. Crucially, this predominance of cognitive co-activation for shaping functional connectivity is systematically obliterated across five datasets of pharmacological and pathological perturbations of consciousness (chronic disorders of consciousness; anaesthesia with sevoflurane, propofol, or ketamine) when cognition is disconnected from the environment or altogether abolished. Altogether, we show that multimodal predictors of functional architecture shift away from cognitive co-activation and toward anatomicalmolecular constraints during pharmacological and pathological perturbations of consciousness.

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Functional connectome harmonics capture early brain organization and maturity in neonates

The functional organization of the human brain is established early, yet the ontogeny of its large-scale functional gradients remains unclear. Using resting-state fMRI data from 714 neonates in the Developing Human Connectome Project, we mapped neonatal brain gradients via functional connectome harmonics (FCH). We identified adult-like sensory-to-multimodal and cognitive gradient patterns present at birth. Applying three FCH-derived metrics--entropy, power, and energy--we found that power and energy were higher in term-born compared to preterm neonates, while entropy was elevated in preterms. These metrics predicted up to ~30% of postmenstrual age, indicating their biological relevance. Our findings reveal that the neonatal brain possesses a robust gradient architecture underpinning early functional organization, offering novel biomarkers for assessing brain maturity and the impact of prematurity on neurodevelopment.

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Acute perilesional excitability explains long-term motor recovery after stroke

Stroke is a leading cause of disability, and changes in neuronal excitability in perilesional regions may critically influence patients recovery. While reduced excitability is often associated with impaired recovery, increased excitability following injury may support reparative mechanisms. Although animal studies have shown how synaptic transmission adapts after stroke, a mechanistic understanding of how these excitability changes in the perilesional area relate to recovery in acute patients remains unclear. Here, we apply patient-specific (N = 96) computational whole-brain models to infer regional excitability, focusing on both perilesional and non-perilesional sites. Specifically, we estimate the firing sensitivity of local excitatory neuronal populations. Our findings indicate large inter-subject variability, with patients displaying both relative perilesional hypo- and hyper-excitability. Notably, perilesional excitability emerges as a robust predictor (P = 0.002) of motor recovery one year after the stroke, but not of acute post-stroke motor impairment, emphasizing its significance in specifically shaping long-term recovery. This synaptic modulation of excitability exhibits a strong correlation with gamma-aminobutyric acid A (GABA-A) receptor density distributions before the stroke, providing a potential biological substrate. These findings highlight the subject-specific nature of perilesional excitability, positioning it as a compelling target for personalized interventions to optimize post-stroke motor recovery.

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Disruption of Striatal Intrinsic Ignition in Huntington's Disease: an In-Silico Perturbational Approach to Emulate Disease Progression and Recovery

Huntingtons disease (HD) is a neurodegenerative disorder caused by a single gene that severely affects motor, cognitive, and behavioral functions and is ultimately fatal. While disruptions in the structural integrity of the striatum are well documented, less is known about how the underlying functional impairments relate to the disease. We developed a large-scale modeling framework based on intrinsic ignition to uncover functional anomalies during HD progression. We first measured how much a spontaneous event in one brain region influences the rest of the brain, then systematically perturbed the activity of the striatum to predict the empirical changes in functional connectivity (FC) by re-optimizing the model parameters and conducting in-silico experiments. Results showed that disruption of the activity dynamics in the caudate, and to some extent the putamen, are the key factors that explain a substantial amount of the variance in FC alterations during HD progression. We then assessed the ability to recover whole-brain functional activity by driving the caudate and putamen activity towards a healthy-like regime and found that, by tuning the local bifurcation parameter of caudate and putamen, it is possible to recover whole-brain healthy functional activity, albeit moderately. Surprisingly, although the functional disruptions in the caudate better explained the alterations in FC, the recovery of the dynamics was more effective in the putamen. Overall, our results suggest that the disruptions of the dynamics in the striatum can explain the gross functional connectivity changes in HD. Our study demonstrates that computational modeling is an important tool to reveal the underlying patterns behind the observed data and provides an opportunity to test interventional mechanisms in silico.

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Large Scale Functional and Effective Connectivity Alterations cross the Huntington's Disease Integrated Staging System

Huntingtons disease (HD) is a progressive neurodegenerative disease with severe motor, cognitive and behavioral symptoms. There is a recent impetus to develop treatments that slow progression before clinical signs emerge. Such early interventions require biomarkers sensitive to the very earliest HD progression. Here we applied cutting-edge fMRI analysis on data collected in the Track-On HD study to evaluate whether functional and effective connectivity obtained from model-free and model-based approaches can produce useful biomarkers of HD progression. We analyzed data from 231 participants with up to three annual visits each and created five groups comprising normative controls and four HD groups according to the Huntingtons Disease Integrated Staging System (HD-ISS). We found significant differences across the HD-ISS stages but not in their longitudinal change. Specifically, we found attenuated functional and effective connectivity in the caudate nucleus in HD-ISS-2, and this effect extended to other corticostriatal connections in HD-ISS-3. Overall, most of the alterations were only evident in advanced HD stages, and we did not observe widespread alterations in cortical connectivity and graph topography. Although HD-ISS groups did not differ in the amount of in-scanner motion, we did find measures of functional and effective connectivity to be sensitive to motion. We conclude that fMRI can indeed capture attenuation of cortico-striatal functional and effective connectivity across HD progression. This is the first study to investigate fMRI alterations across the recently created HD-ISS stages within a novel framework of signal flow across the whole brain.

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The Turbulent Brain: a toolbox to compute the turbulent dynamical behaviour of whole-brain activity

Brain disorders remain one of the greatest challenges in neuroscience. Computational precision medicine offers a promising framework to reveal the mechanistic principles governing both healthy and pathological brain dynamics. In this context, we present The Turbulent Brain (TTB) toolbox, an open-source MATLAB platform that implements and disseminates the turbulence framework for immediate and widespread application in neuroscience research. The toolbox combines model-free and model-based analyses through an intuitive graphical interface, enabling customizable workflows across different parcellations and preprocessing pipelines. Our toolbox builds on recent advances demonstrating that turbulence physics can effectively capture the complex spatiotemporal dynamics of brain activity as a high-dimensional system operating far from equilibrium. This framework allows researchers to explore how fundamental mechanisms are modulated across distinct brain states and neurological and psychiatric disorders, including disorders of consciousness and major depressive disorder. As an illustrative application case, we used TTB to analyse fMRI data from 176 individuals from the Human Connectome Project during resting state and movie watching, showing that movie watching, as compared to resting state, significantly reduces information transmission in terms of turbulence measures, with stronger reductions observed during Creative Commons movie watching compared to Hollywood movies. In summary, the TTB toolbox establishes an accessible framework providing a methodological bridge between nonlinear physics and computational neuroscience, offering new tools for investigating psychiatric conditions and altered states of consciousness.

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Disrupted hierarchical organization in disorders of consciousness revealed by fluctuation-dissipation deviations

Evaluating consciousness levels after coma remains clinically challenging, and probing the brains functional hierarchy offers model-based biomarkers of brain states. We characterize the hierarchy loss in disorders of consciousness (DoC) via departures from non-equilibrium dynamics. Irreversible, directed interactions are indexed by deviation from the fluctuation- dissipation theorem (FDT), computed from individualized whole-brain models fit to fMRI from controls and patients in minimally conscious state (MCS) or unresponsive wakefulness syndrome (UWS). Global and resting-state network dynamics in DoC were closer to equilibrium than in controls, decreasing stepwise with decreasing levels of consciousness. Mapping site-specific hierarchical drive over the system revealed disruptions within default-mode network components (e.g., medial and dorsolateral superior frontal gyrus) and subcortical hubs (e.g., thalamus, pallidum and putamen) differentiating between all groups. Recovery of near-control hierarchy in the visual network differentiated MCS from UWS, whereas multiple limbic areas showed similar abnormalities across both DoC groups. Together, these results identify non-equilibrium dynamics as a signature of conscious capacity and stablish FDT deviation as a principled, model-based hierarchy measure that can be operationalised for clinical stratification and monitoring, opening avenues for targeted in silico intervention planing.

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Whole-Brain Models of Minimal Phenomenal Experience: Approaching Criticality through Jhana Meditation

Advanced meditation offers a powerful lens for investigating consciousness and for understanding how sustained training may contribute to human flourishing. In the spirit of neurophenomenology, we combine first-person reports with model-free empirical analyses and formal whole-brain modeling to investigate the mechanisms underlying advanced meditative states and minimal phenomenal experience (MPE). Specifically, we focus on jh[a]na meditation, a type of advanced concentrative absorption meditation (ACAM-J). Advanced practitioners accessed the eight ACAM-J states during ultra-high-field 7T functional magnetic resonance imaging. For each state, we first characterize empirical functional connectivity and then build a mechanistic whole-brain model that reproduces brain activity by modeling the dynamical regimes of different brain networks. We found that the later ACAM-J states, taken here as candidates for MPE, show increased large-scale functional integration and a shift of functional network dynamics toward near-critical working points. The default mode network (DMN) exhibits the largest shift, from a distant noise-driven regime during the control condition to near-critical dynamics during ACAM-J. We also observed that the trajectory of ACAM-J states is non-linear, with prominent reconfigurations at key meditative milestones. Our results suggest that MPE, as instantiated in later ACAM-J states, corresponds to a globally susceptible state where near-critical dynamics dominate. We interpret this near-critical regime as a form of "openness", in which constrained and differentiated patterns of brain activity give way to greater flexibility. In particular, increased DMN susceptibility is correlated with broader attention and reduced narrative thought, consistent with a more flexible mode of self-related processing. In this context, advanced meditation provides a powerful model for studying how sustained contemplative practice can profoundly shape brain dynamics and provide a window into core aspects of consciousness.

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Physical exercise and brain network dynamics: reduction of frontoparietal-striatal connectivity following 1 hour of aerobic cycling

Physical exercise is beneficial for metabolic health and cognitive performance. In addition, exercise can be highly pleasurable and and serves as an effective stress reliever. Extant studies have highlighted frontal, parietal, and subcortical brain changes following acute bouts of exercise. However, slower, slightly delayed brain correlates after exercise at the network level have not been studied. Therefore, this studys objective was to investigate the changes in dynamic functional connectivity after 60 minutes of exercise in healthy males. Here we measured a 6-minute resting state fMRI in 24 young males at baseline and after a 60-minute cycling exercise challenge. Apart from routine preprocessing, the data were denoised with FSL-FIX and modeled with i) leading eigenvector dynamics analysis (LEiDA) to probe whole brain network dynamics and ii) with group independent component analysis (ICA) and dual regression to quantify static brain connectivity. The within subject statistical tests compared baseline to post-exercise conditions. We found that a striato-fronto-parietal network is destabilized after exercise, as indicated by a lower probability of occurrence in dynamic analysis through LEiDA. The brain areas in the network include the bilateral caudate, putamen and pallidum as well as middle orbitofrontal, frontal operculum, frontal trigonum and inferior parietal cortices. No differences between baseline and post exercise conditions were found in the dual regression of the group ICA components. We conclude that 60 minutes of cycling causes a prolonged effect in brain network dynamics, reducing synchronization between the striatum and frontoparietal networks with respect to baseline. This provides insights into the network-level neural correlates of aerobic exercise, which may be directly linked with the stress relieving effects of physical exercise.

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Inception: Simulating Personalized Long-Term Recovery in Disorders of Consciousness using Whole-Brain Computational Perturbations

Advancements in the treatment of Disorders of Consciousness have seen significant progress with per-turbative techniques and pharmacological therapies. Despite their potential, the underlying mechanisms of their variable efficacy remain poorly understood. To address this challenge, recent studies have utilised whole-brain modelling to simulate in silico perturbations. However, existing models focus exclusively on system behaviour during active stimulations, leaving unexplored how the brain dynamics evolve in post-acute and long-term stages, crucial in the recovery of consciousness. Here, we introduce Inception, a novel personalized approach to in silico perturbation modelling. We use a whole-brain models to simulate the perturbations and to unravel information about the long term effects of the proposed intervention. Applied to fMRI data from patients in a minimally conscious state and an unresponsive wakefulness state, our approach effectively simulates the transition to a healthy state, generating perturbed data closely resembling healthy brain activity. Moreover, we show that Inception enhances patient classification through machine learning, outperforming functional connectivity-based approaches. Finally, we investigate the correlation between perturbation responses and brain neuroreceptors, proposing that Inception might capture the long-term effects of pharmacological interventions in Disorders of Consciousness treatment.

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The synergistic interactions of low-dimensional brain modes

Neuroimaging techniques produce vast amounts of data, capturing brain activity in a high-dimensional space. However, brain dynamics are consistently shown to reside in a rather lower-dimensional space, which contains relevant information for cognition and behavior. This dimensionality reduction reflects distinct types of interactions between brain regions, such as redundancy -shared neural information distributed across regions- and synergy, where information emerges only when regions are considered collectively. Significant efforts have been devoted to developing linear and non-linear algorithms to reveal these low-dimensional dynamics, often termed "brain modes." Here, we apply various dimensionality reduction techniques to resting-state functional magnetic resonance imaging (fMRI) data from 100 healthy participants to examine how synergistic interactions in brain dynamics are preserved by these techniques. We first demonstrate that biologically informed brain parcellation modulates and preserves synergy-dominated interactions. Next, we show that synergy among low-dimensional modes enhances functional-connectivity reconstruction: nonlinear autoencoders not only achieve the lowest reconstruction error but also maximally preserve synergy, outperforming principal component analysis, diffusion maps, and Laplacian eigenmodes. Finally, we confirm previous results suggesting that global signal regression helps to identify synergistic interactions between regions. Our findings establish synergy preservation as a complementary criterion to reconstruction accuracy, highlighting autoencoders as a nonlinear tool for uncovering synergistic low-dimensional brain modes from high-dimensional neuroimaging data.

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Evolution's boldest trick: Neurotransmission modulated whole-brain computation captures full task repertoire

The perhaps most important unsolved problem in neuroscience is how the brain survives in a complex world by performing a rich repertoire of computation on a minimal energy budget. The brain is much better at adapting to the multiplicity of stimuli and outcomes than current generations of computers, artificial neural deep learning and reservoir model architectures. Yet, at first glance the brain appears to use a fixed anatomical architecture to perform the necessary huge variety of computations. But evolutions boldest trick is that in fact the brains effective connectivity is constantly being updated through neuromodulation to allow the rich repertoire of computation. Inspired by this, we created a whole-brain model using empirical neurotransmitter maps modulating the underlying local regional dynamics. This NEMO (neurotransmission modulated) whole-brain model is able to flexibly compute the full task repertoire and associated functional connectivity of the neuroimaging data from 971 healthy participants. For each individual we defined a measure of brain computability as the fitting of the NEMO whole-brain model to all tasks performed by the individual. Importantly, brain computability correlates with both behavioural performance on individual tasks and with a general behavioural measure of intelligence. Overall, our proposed unifying NEMO framework offers a natural way to sculpt different brain dynamics in a fixed brain architecture to compute the rich repertoire of tasks required for surviving and thriving.

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An engine for systematic discovery of cause-effect relationships between brain structure and function

Characterising how perturbations of brain architecture influence brain function is essential to understand the origins of brain dysfunction, and devise potential avenues of treatment. Here we introduce a computational engine for systematic causal discovery of the functional consequences of altering network architecture and local biophysics in the brain. We integrate multimodal anatomical and functional neuroimaging to implement over 2, 000 in-silico brains, and provide mechanistic insight into the functional consequences of local lesions, global wiring, and empirically-derived maps of regional cytoarchitecture and chemoarchitecture. We comprehensively assess how each manipulation of brain macrostructure reshapes spatial and temporal signal coordination, information dynamics, and functional hierarchy--as well as spontaneous co-activation of meta-analytic cognitive circuits, and > 6, 000 dimensions of local neural dynamics. Our computational model systematically identifies which features of brain architecture have overlapping or antagonistic causal influence over each dimension of brain function, and how functional properties are traded off against each other across disorders and neuromodulation. We find that regions functional vulnerability to lesions in silico recapitulates their vulnerability to neurodevelopmental and psychiatric in vivo, along a core-periphery organisation. We provide convergent evidence that the brains wiring diagram is finely tuned to favour the hierarchical integration of information. Notably, our model successfully recapitulates known empirical results that have not been modelled before, including desynchronisation and flattening of the brains functional hierarchy induced by psychedelic 5HT2A agonists. To catalyse future discoveries, we make this resource freely available to the neuroscience community through an interactive website (https://systematic-causal-mapping.up.railway.app/), where users can interrogate our systematic database of simulated cause-effect relationships. Altogether, we provide a powerful computational engine to predict the functional consequences of experimental or clinical interventions, and drive neuroscientific hypothesis-generation.

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Cross-Frequency Coupling as a Neural Substrate for Prediction Error Evaluation: A Laminar Neural Mass Modeling Approach

Predictive coding frameworks suggest that neural computations rely on hierarchical error minimization, where sensory signals are evaluated against internal model predictions. However, the neural implementation of this inference process remains unclear. We propose that cross-frequency coupling (CFC) furnishes a fundamental mechanism for this form of inference. We first demonstrate that our previously described Laminar Neural Mass Model (LaNMM) supports two key forms of CFC: (i) Signal-Envelope Coupling (SEC), where lowfrequency rhythms modulate the amplitude envelope of higher-frequency oscillations and (ii) Envelope-Envelope Coupling (EEC), where the envelopes of slower oscillations modulate the envelopes of higher-frequency rhythms. Then, we propose that, by encoding information in signals and their envelopes, these processes instantiate a hierarchical "Comparator" mechanism at the columnar level. Specifically, SEC generates fast prediction-error signals by subtracting top-down predictions from bottom-up oscillatory envelopes, while EEC operates at slower timescales to instantiate gating--a critical computational mechanism for precision-weighting and selective information routing. To establish the face validity and clinical implications of this proposal, we model perturbations of these CFC mechanisms to investigate their roles in pathophysiological and altered neuronal function. We illustrate how, in disorders such as Alzheimers disease, disruptions in gamma oscillations following dysfunction in fast-spiking inhibitory interneurons impact Comparator function with an aberrant amplification of prediction errors in the early stages and a drastic attenuation in late phases of the disease. In contrast, by increasing excitatory gain, serotonergic psychedelics diminish the modulatory effect of predictions, resulting in a failure to attenuate prediction error signals (c.f., a failure of sensory attenuation). Collectively, these findings implicate cross-frequency coupling across multiple temporal scales as a key computational mechanism supporting predictive coding and suggest that disruptions in these processes play a central role in disease. HighlightsO_LIUsing an encoding scheme where information is encoded in signals, their envelopes, and envelopes of envelopes, we show how to implement prediction error and precision modulation in a neural mass model through cross-frequency coupling (CFC). C_LIO_LIWe use the laminar neural mass model (LaNMM), which integrates Jansen-Rit and pyramidal interneuron gamma (PING) submodels to display fast and slow rhythms and provides mechanisms for a) Signal-Envelope Coupling (SEC), where slow-wave activity modulates the amplitude envelope of fast oscillations (analogous to phase-amplitude coupling), and b) Envelope-Envelope Coupling (EEC), where the envelopes of slower oscillations modulate the envelopes of higher-frequency rhythms. C_LIO_LIWe show how to use the LaNMM to implement information-based prediction-error evaluation (as used in Active Inference and Kolmogorov Theory), computing the approximate precision-weighted difference between incoming sensory data (envelopes) and internal model predictions (signals or envelopes). C_LIO_LIWe show that using these mechanisms, the Comparator mechanism can operate at multiple levels and timescales, generating fast prediction-error signals (via SEC) and slower gating signals that encode context (e.g., precision) (via EEC). C_LIO_LIOur model provides insights into the physiological and cognitive consequences of mesoscale circuital alterations in the context of predictive coding. First, we study disorders of fast-spiking interneurons, such as Alzheimers Disease (AD). In the early stages of AD, error evaluation and precision are disrupted (inflated error and reduced gating/weight of predictions), leading to higher prediction errors. In later stages, prediction errors are suppressed regardless of predictions or their precision. C_LIO_LIThen, we show how serotonergic psychedelics increase the effective weight of inputs and diminish that of predictions, resulting in higher prediction error signals. C_LIO_LIThese observations link oscillatory mechanisms and predictive coding alterations, and potentially with the subjective phenomena in each condition--including cognitive decline in AD and hallucinatory states under psychedelics. C_LI

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