Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.04.30.651283

Frequency-Dependent Neurostimulation in Whole Brain Network models

Abstract

BackgroundBrain stimulation at specific frequencies has been shown to have therapeutic effects for certain neurological disorders. However, it remains unclear how these oscillatory inputs interact with neuronal dynamics and what drives this frequency selectivity. Here, we propose that this is achieved by targeting specific brain circuits through frequency-selective network entrainment. MethodsTo demonstrate that this type of entrainment can occur in the brain connectome structure, we use a minimal physics-based model of coupled oscillators that preserves only the essential structural connectivity of real brain networks. Using this model, we test how periodic stimulation influences network oscillatory dynamics, identifying sub-networks that synchronize with specific stimulation frequencies. Furthermore, we validate the suitability of the model to reproduce well-known frequency-selective entrainment using visual and auditory periodic stimulation. ResultsOur model reproduces selective network entrainment, whereby distinct stimulation frequencies favor the synchrony of different sub-networks. Crucially, entrainment exhibits a physics-predicted inverse relationship with frequency: lower-frequency stimulation favors broader synchrony across the network, while higher-frequency inputs produce spatially confined effects. These patterns emerge purely from network structure and oscillatory physics, independent of biological details. ConclusionThis physics-based approach elucidates the fundamental mechanistic principles governing frequency-selective brain network stimulation. Our minimal model demonstrates that selective entrainment of specific subnetworks can be achieved through frequency selection alone, largely determined by network structure and oscillatory dynamics. These findings provide a theoretical foundation for understanding how network architecture determines stimulation selectivity, supporting the development of principled approaches to targeted neuromodulation. Author summaryIn this work, we explore how external rhythmic stimulation interacts with the brains own rhythms. We use a physics-based model that represents the brain as a network of interconnected oscillators, linked according to the human connectome. Through this model, we show that stimulation effects are not limited to the targeted region but spread across the network, depending on the stimulation frequency, its spatial location and the underlying network dynamics. Our results reveal that low-frequency rhythms promote large-scale synchrony, while high-frequency rhythms engage more localized areas, all emerging from the brains structural connections and communication delays. The simulated cortical activation exhibits a frequency-selective profile that aligns strongly with that estimated from sensory-evoked electroencephalographic activity. This agreement suggests that differences between individuals in how their brain networks operate may explain why stimulation affects each person differently. Our findings offer a mechanistic framework for designing personalized stimulation protocols, illustrating how computational modeling can guide the optimization of noninvasive brain stimulation in both research and clinical contexts.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Otero, M., Poo, E., Torres, F., Mendoza, C., Lea-Carnall, C. A., Weinstein, A., Guevara, P., Prado, P., Cabral, J., EL-DEREDY, W.. 2025-05-04. Frequency-Dependent Neurostimulation in Whole Brain Network models. https://doi.org/10.1101/2025.04.30.651283

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Synergy-informed bilevel optimization reveals joint-specific benefits for realistic exoskeleton torque prediction

Simulation-driven optimization can guide exoskeleton control design, but its utility is limited by the accuracy with which muscle coordination is predicted. Strict effort-minimization formulations predict non-physiological muscle shutdown under high exoskeleton assistance, leading to peak assistive torques that exceed values reported in human-in-the-loop experiments. We evaluated the accuracy of synergy-informed simulations at predicting assistance across four single-joint exoskeleton configurations: ankle plantarflexion, knee extension, hip flexion, and hip abduction. We implemented a bilevel optimization to predict a parameterized assistive torque that minimizes metabolic cost, with assisted muscle dynamics estimated via either effort-minimization simulations (minimizing muscle effort only) or synergy-informed simulations (minimizing muscle effort constrained to a synergy structure). We used experimental data from five unimpaired adults walking at their preferred speed and compared results descriptively between the two formulations within each subject. Assistance based on effort-minimization simulations shut down agonist muscle activations and overestimated peak assistive torque compared with experimental values. In contrast, constraining muscle controls to a synergy structure prevented non-physiological muscle shutdown and yielded assistive torques closer to those measured in human-in-the-loop experiments. This benefit was not observed equally across all assisted degrees of freedom or subjects, emerging only where no single synergy could be suppressed to unload the assisted muscles. Synergy weights can therefore be interpreted as joint-specific predictors of when simulations can reliably inform wearable robot design.

bioengineering↗

Engineered microvessel networks -- Longitudinal transcriptomic profiling validates chip-grown tissues as a robust model for studying vasculature

Vascularised Organ-on-Chip (OoC) models are promising New Approach Methodologies (NAMs), but their translation requires validation for defined Contexts of Use (CoU). Here, we combine microfluidic microvessel networks (MVNs) with longitudinal bulk and single-cell RNA sequencing to determine how cell provenance influences engineered vascular phenotype. Stromal cell identity produced distinct network architectures and transcriptional trajectories, demonstrating that support cells, commonly treated as interchangeable, represent an important CoU variable. Primary human pancreatic microvascular endothelial cells failed to form stable perfusable networks, but supplementation with 10% Human Umbilical Vein Endothelial Cells (HUVECs) or Blood Outgrowth Endothelial Cells (BOECs) rescued self-assembly. Single-cell transcriptomics identified specialised endothelial populations associated with vascular morphogenesis, including tip, stalk, phalanx, endothelial to mesenchymal transition (EndMT) and pericyte-like endothelial cells. Failed networks lacked coherent endothelial specialisation, whereas rescued networks restored stabilising cell states and revealed FLRT2--UNC5B signalling within pericyte-like HUVECs, recapitulating a pathway implicated in angiogenic development in vivo. These findings establish cell provenance as a critical determinant of microvascular NAM performance and demonstrate how transcriptomic validation can define and strengthen the biological relevance of microvessel-on-chip models for specific CoUs.

bioengineering↗

Benchmarking foundation models for resting-state functional magnetic resonance imaging time series in cognitive aging research

Foundation models trained on large neuroimaging datasets could help smaller studies investigate cognition from brain recordings. However, whether the foundation model-derived representations improve assessment of current cognition, prediction of follow-up cognition, or characterization of cognitive change remains unclear. We evaluated nine configurations from five model families that process regional resting-state functional magnetic resonance imaging time series, using 3,103 scans from 1,653 participants across two observational and five intervention aging cohorts. Primary frozen representations showed no consistent superiority over conventional functional connectivity for concurrent cognitive associations or diagnostic classification. Changing the readout improved selected concurrent cognitive associations without updating model weights, indicating that performance depended partly on how representations were extracted. Additional post-training and embedding alignment yielded gains in selected settings but did not consistently improve performance across outcomes. In the primary longitudinal analyses, imaging representations did not establish added value beyond baseline clinical measures. These findings show that readout choice influences concurrent cognitive associations, while the added value of these representations for longitudinal outcomes remains unestablished.

bioengineering↗