Enterprise AI Analysis
Intensity-dependent tACS entrainment effects in a cortical microcircuit: a computational study
This computational study investigates how transcranial alternating current stimulation (tACS) influences neural activity in a cortical microcircuit, integrating realistic neuronal morphologies and synaptic connectivity. Our model reveals that tACS primarily modulates spike timing, rather than firing rates, and that pyramidal neurons are more sensitive to external electric fields than interneurons due to their distinct morphologies. The study highlights a dual effect: low-intensity tACS can disrupt endogenous oscillations, while higher intensities enhance neural entrainment, leading to stable phase locking. This complex interplay between intrinsic neuronal properties, network dynamics, and stimulation intensity underscores the importance of optimized tACS parameters for precise neuromodulation in clinical and research settings. The findings provide critical insights into the cellular and network-level mechanisms of tACS-induced entrainment.
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Transcranial alternating current stimulation (tACS) is a promising noninvasive technique for modulating neural oscillations, enhancing cognitive functions, and alleviating symptoms of psychiatric disorders. However, its efficacy is debated due to the critical influence of neuronal morphology and microscopic factors on responses to external electric fields. This study developed a cortical microcircuit model to investigate cellular- and network-level mechanisms of tACS-induced neural entrainment.
Key Finding
15 Second duration sufficient for immediate entrainment effectsComputational Modeling Process
Pyramidal Cells vs. Interneurons to tACS
| Feature | Pyramidal Cells | Interneurons |
|---|---|---|
| Morphology | Elongated, directionally oriented dendritic trees | Lack elongated dendritic trees |
| EF Sensitivity | High sensitivity, align to rising anodic phase | Lower and less consistent entrainment |
| PLV Response (Alpha Band) | Linear relation with tACS intensity (R² > 0.9) | Weak linearity (R² < 0.1, except L4 LBC) |
| Phase Stability | Stabilize preferred phases at ≥ 1 mA | Greater variability in preferred phases |
| Primary Influence | Direct EF effects and synaptic inputs | Synaptic interactions more dominant than direct EF |
The study found that tACS primarily modulates spike timing without significantly altering overall firing rates, consistent with experimental and computational studies. Pyramidal neurons, due to their distinct morphologies, exhibited a clearer and more linear relationship between phase-locking value (PLV) and tACS intensity compared to interneurons. This highlights dendritic morphology as a critical determinant of a neuron's sensitivity to external electric fields.
Key Finding
~0.1 PLV increase linked to enhanced working memory (rodent studies)tACS effects on neural entrainment are mediated by a complex interplay between intrinsic neuronal properties and network dynamics. Synchronization in LFPs increased with higher tACS amplitudes. When intrinsic firing rates were matched (theta oscillations), LFP synchronization increased rapidly, whereas with heterogeneous intrinsic rates (alpha band), synchronization emerged more gradually. This suggests that the degree and speed of tACS-induced entrainment depend on endogenous network dynamics.
Optimizing tACS for Therapeutic Outcomes
The dual effect of tACS—where low intensity can disrupt endogenous oscillations, and higher intensity leads to stable entrainment—is crucial for therapeutic optimization. For conditions like Parkinson's disease, characterized by excessive synchrony (PLVs up to 0.36), tACS could be configured to disrupt pathological rhythms. Conversely, for cognitive enhancement (e.g., working memory, linked to ~0.1 PLV increase), tACS would aim to enhance beneficial synchrony. Understanding this intensity-dependent response is key to designing precise neuromodulation protocols tailored to specific clinical goals.
The findings underscore the importance of neuronal morphology and network interactions in determining tACS responses, providing insights that may help optimize stimulation parameters for precise neuromodulation in both clinical and research settings. Future work should focus on developing multi-scale models that connect cellular, network, and whole-brain dynamics to optimize electrode montages and stimulation protocols for improved efficacy.
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