Prospects on Clinical Applications of Electrical Stimulation for Nerve Regeneration
Overview
Cell Biology
Authors
Affiliations
Regenerative capability is limited in higher vertebrates but present in organ systems such as skin, liver, bone, and to some extent, the nervous system. Peripheral nerves in particular have a relatively high potential for regeneration following injury. However, delay in regrowth or growth, blockage, or misdirection at the injury site, and growth to inappropriate end organs may compromise successful regeneration, leading to poor clinical results. Recent studies indicate that low-intensity electrical stimulation is equivalent to various growth factors, offering avenues to improve these outcomes. We present a review of studies using electric and electromagnetic fields that provide evidence for the enhancement of regeneration following nerve injury. Electric and electromagnetic fields (EMFs) have been used to heal fracture non-unions. This technology emerged as a consequence of basic studies [Yasuda, 1953; Fukada and Yasuda, 1957] demonstrating the piezoelectric properties of (dry) bone. The principle for using electrical stimulation for bone healing originated from the work of Bassett and Becker [1962], who described asymmetric voltage waveforms from mechanically deformed live bone. These changes were presumed to occur in bone during normal physical activity as a result of mechanical forces, and it was postulated that these forces were linked to modifications in bone structure. Endogenous currents present in normal tissue and those that occur after injury were proposed to modify bone structure [Bassett, 1989]. These investigators proposed that tissue integrity and function could be restored by applying electrical and/or mechanical energy to the area of injury. They successfully applied electrical currents to nonhealing fractures (using surgically implanted electrodes or pulsed currents using surface electrodes) to aid endogenous currents in the healing process.(ABSTRACT TRUNCATED AT 250 WORDS)
Cellular Mechanisms of Electromagnetic Field in Traumatic Brain Injury.
Siddiqi I, Marino M, Agrawal D, Baron D, Connett D, Miulli D J Biotechnol Biomed. 2023; 6(2):95-104.
PMID: 37388676 PMC: 10310312. DOI: 10.26502/jbb.2642-91280075.
Huang L, Sun X, Wang L, Pei G, Wang Y, Zhang Q MedComm (2020). 2022; 3(3):e160.
PMID: 35949547 PMC: 9350428. DOI: 10.1002/mco2.160.
Multifunctional GelMA platforms with nanomaterials for advanced tissue therapeutics.
Kurian A, Singh R, Patel K, Lee J, Kim H Bioact Mater. 2021; 8:267-295.
PMID: 34541401 PMC: 8424393. DOI: 10.1016/j.bioactmat.2021.06.027.
He S, Tripanpitak K, Yoshida Y, Takamatsu S, Huang S, Yu W J Pain Res. 2021; 14:1785-1807.
PMID: 34163235 PMC: 8215851. DOI: 10.2147/JPR.S311559.
Anti-apoptotic effect of adipose tissue-derived stromal vascular fraction in denervated rat muscle.
El-Habta R, Andersson G, Kingham P, Backman L Stem Cell Res Ther. 2021; 12(1):162.
PMID: 33663595 PMC: 7934515. DOI: 10.1186/s13287-021-02230-y.