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Gerardos, G.

Publications and source records attributed to Gerardos, G..

3 recordsLinked to original sources

Cortical Stimulation Strength and sgACC Connectivity Shape Neuro-Cardiac Responses to Prefrontal TMS

Autonomic dysregulation is a core feature of major depressive disorder and a promising physiological readout for early signs of clinical effectiveness of therapeutic TMS targeting prefrontal regions. Yet the stimulation dose and network properties required to optimally engage autonomic circuits remain elusive. Here, we applied a cortex- and circuit-centered dosing framework combining resting-state fMRI, simulations of the TMS-induced electric field, and electrocardiography acquired during repetitive TMS of six left dorsolateral prefrontal cortex (DLPFC) targets in healthy adults. Heart-brain coupling (HBC), defined as spectral power in the cardiac response locked to the TMS onset frequency, was modeled as a function of either conventional motor-threshold-based dose or cortical electric-field strength, with and without DLPFC connectivity to the subgenual anterior cingulate cortex (sgACC). Across linear and nonlinear models, cortical electric-field dose explained substantially more variance in HBC, indicating that prefrontal TMS dosing is best assessed at the cortical level. Incorporating sgACC connectivity further improved model fit and revealed site-specific electric-field-by-connectivity interactions, with the strongest and most reliable HBC modulation at DLPFC regions anticorrelated with sgACC. Voxel-wise TMS mapping identified individualized cortical hotspots spatially overlapping with sgACC-anticorrelated tissue. Notably, whereas negative connectivity showed the most robust and monotonic effects, nonlinear dose-response analyses suggested a confined stimulation range over which positively connected sites also exhibited HBC modulation. Together, these findings position HBC as a network-sensitive physiological readout of DLPFC-sgACC-vagal engagement and offer a principled answer to where and how much to stimulate, supporting an electric-field- and connectivity-informed dosing framework for refining prefrontal TMS in depression-related autonomic dysregulation.

neuroscience↗

EthoPy: Reproducible Behavioral Neuroscience Made Simple

As brain activity is tightly coupled to behavior, an accurate understanding of neural function necessitates consideration of behavioral tasks that capture the complexity and variety animals encounter. Nevertheless, animal training for behavioral experiments is often labor-intensive, costly, and difficult to standardize. To overcome these challenges, we developed EthoPy, an open-source, Python-based behavioral control framework that integrates stimulus presentation, hardware management, and data logging. EthoPy supports diverse behavioral paradigms, stimulus modalities, and experimental systems, from homecage to head-fixed configurations, while operating on affordable hardware, such as Raspberry Pi. Its modular architecture and database integration enable scalable, high-throughput automatic behavioral training with minimal experimenter involvement while ensuring reproducibility through comprehensive metadata tracking. By automating training workflows, EthoPy makes it feasible to implement sophisticated behavioral paradigms that are traditionally difficult to achieve. EthoPy thus provides an accessible, extensible framework to study behavior and the underlying neural activity.

animal behavior and cognition↗

Target-Specificity and Repeatability in Neuro-Cardiac-Guided TMS for Heart-Brain Coupling

The dorsolateral prefrontal cortex (DLPFC) is a principal target for transcranial magnetic stimulation (TMS) in treating major depressive disorder, with therapeutic effects thought to be mediated by its connectivity with the subgenual anterior cingulate cortex. As both regions are involved in autonomic regulation, short-term heart rate changes following DLPFC stimulation may serve as physiological markers to identify stimulation targets. We employed neuro-cardiac guided TMS in a cohort of healthy participants to examine the effects of stimulation intensity and DLPFC target specificity on heart-brain coupling (HBC). We used generalized additive models to assess nonlinear effects of stimulation intensity and target location on HBC, while accounting for pain ratings and other side effects. Intra-subject repeatability across three sessions was evaluated using intraclass correlation coefficients. We observed a non-linear modulation of HBC depending on stimulation intensity and target location, with greater effects at the F3 lateral and F3 posterior targets compared to sham. By evaluating these effects across sessions within participants, we demonstrate the robustness of our results beyond the influence of pain and other side effects on HBC modulation. Exploratory analyses of the directionality show a consistent decrease in HR only at the F3 lateral target with suprathreshold stimulation. These results demonstrate that HBC is modulated in a target- and intensity-specific manner, with particularly consistent effects at F3 lateral sites within the DLPFC. The findings enhance the understanding of TMS-modulated heart-brain interactions, offering a potential framework for optimizing individualized rTMS treatment protocols for depression.

neuroscience↗