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Updated: Jun 30, 2025

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Dorsal Root Ganglion Injection and Dorsal Root Crush Injury as a Model for Sensory Axon Regeneration
Published on: May 3, 2017
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Computational modeling of dorsal root ganglion stimulation using an Injectrode.
Sauradeep Bhowmick1,2, Robert D Graham1,2, Nishant Verma3,4
1Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States of America.
Journal of Neural Engineering
|March 19, 2024
Summary
The Injectrode device shows promise for dorsal root ganglion (DRG) stimulation. Larger Injectrode surface areas improve therapeutic margins by selectively activating Aβ-fibers while avoiding Aδ-fiber pain responses.
Area of Science:
- Neuromodulation
- Biomedical Engineering
- Computational Neuroscience
Background:
- Minimally invasive neuromodulation offers a low-risk approach for electrical stimulation.
- The Injectrode, a flexible microcoil electrode, is designed for dorsal root ganglion (DRG) stimulation.
- Transcutaneous electrical stimulation (TES) effectiveness depends on system geometry.
Purpose of the Study:
- To investigate how Injectrode system design parameters influence charge delivery and neural activation.
- To analyze the impact of Injectrode size and orientation on neural activation thresholds.
- To determine optimal configurations for effective DRG stimulation.
Main Methods:
- Hybrid computational modeling using finite element method (FEM) for DRG stimulation.
- Multi-compartment models of DRG neurons to simulate neural responses.
- Analysis of potential distribution and neural activation thresholds under various stimulation parameters.
Main Results:
- Injectrode system predominantly activates large-diameter afferents (Aβ-fibers).
- Activation thresholds are dependent on Injectrode surface area.
- Increased surface area expands the therapeutic margin by reducing charge density and delaying Aδ-fiber activation.
Conclusions:
- The Injectrode is a viable technology for minimally invasive DRG neuromodulation.
- Larger Injectrode surface areas enhance the therapeutic window for selective Aβ-fiber activation.
- Design optimization is crucial for maximizing therapeutic benefit and minimizing off-target effects.

