Development and application of a novel multi-channel in vitro electrical stimulator for cellular research.

BMC biomedical engineering Pub Date : 2025-03-03 DOI:10.1186/s42490-025-00090-8

Jorge R Cibrão, Miguel Armada, Marta F Lima, André Vidinha-Mira, Jonas Campos, Tiffany S Pinho, António J Salgado, Alar Ainla, Nuna A Silva

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Abstract

Background: Exposure to electric fields affects cell membranes impacting their potential and altering cellular excitability, nerve transmission, or muscle contraction. Furthermore, electric stimulation influences cell communication, migration, proliferation, and differentiation, with potential therapeutic applications. In vitro platforms for electrical stimulation are valuable tools for studying these effects and advancing medical research. In this study, we developed and tested a novel multi-channel in vitro electrical stimulator designed for cellular applications. The device aims to facilitate research on the effects of electrical stimulation (ES) on cellular processes, providing a versatile platform that is easy to reproduce and implement in various laboratory settings.

Methods: The stimulator was designed to be simple, cost-effective, and versatile, fitting on standard 12-well plates for parallel experimentation. Extensive testing was conducted to evaluate the performance of the stimulator, including 3D finite element modelling to analyse electric field distribution. Moreover, the stimulator was evaluated in vitro using neuronal and stem cell cultures.

Results: Finite element modelling confirmed that the electric field was sufficiently homogeneous within the stimulation zone, though liquid volume affected field strength. A custom controller was developed to program stimulation protocols, ensuring precise and adjustable current delivery up to 160 V/m. ES promoted neurite outgrowth when applied to SH-SY5Y neural cells or to primary spinal cord-derived cells. In human neuronal progenitor cells (hNPCs), ES enhanced neurite growth as well as differentiation into neurons. In adipose stem cells (ASCs), ES altered the secretome, enriching it in molecules that promoted hNPC differentiation into neurons without enhancing neurite growth.

Conclusions: Our results highlight the potential of this multi-channel electrical stimulator as a valuable tool for advancing the understanding of ES mechanisms and its therapeutic applications. The simplicity and adaptability of this novel platform make it a promising addition to the toolkit of researchers studying electrical stimulation in cellular models.

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