Experimental Analysis and Modeling Study of Impedance Changes in Decellularized and Recellularized Peripheral Nerves

Peripheral nerve injuries pose a significant clinical challenge due to the limited self-repair capacity and the complexity of neural tissue architecture. Tissue engineering strategies applied to the peripheral nerve system aim to restore functional nerve constructs by combining scaffolds, cells, and biochemical cues to recreate the native microenvironment. This work aimed to propose the electrical conductivity as a functional readout of structural and biological remodeling in engineered peripheral nerve scaffolds, along with functional and molecular evaluations. To this end, bioimpedance measurements were combined with equivalent circuit modeling to track state-dependent changes across different levels of tissue organization. Murine sciatic nerves were decellularized and recellularized with neural populations to generate engineered constructs, and their electrical properties were assessed using broadband bioimpedance spectroscopy. Distinct impedance profiles were observed across control, decellularized, and recellularized samples, reflecting structural and functional changes associated with cell removal and repopulation. Furthermore, a multilayer series RC circuit model was implemented to accurately reproduce the measured spectra, enabling the extraction of layer-specific electrical parameters. Analysis of these parameters revealed that decellularization reduces compartmental resistances and increases inter-layer coupling, whereas recellularization restores outer-layer resistances and reduces coupling, consistent with functional tissue organization. Overall, the results demonstrate that bioimpedance provides a readout of the scaffold biological state and cellular integration, and that equivalent circuit modeling offers a quantitative framework to link structural remodeling to electrical function in engineered peripheral nerve tissues.