4.7 Article

Electrical stimulation as a conditioning strategy for promoting and accelerating peripheral nerve regeneration

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EXPERIMENTAL NEUROLOGY
卷 302, 期 -, 页码 75-84

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ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.expneurol.2017.12.013

关键词

Nerve regeneration; Electrical stimulation; Conditioning lesion; Peripheral nerve; Axon regeneration; Microsurgical repair; Regeneration-associated genes; Growth associated protein-43; Brain derived neurotrophic factor; Glial fibrillary acidic protein

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The delivery of a nerve insult (a conditioning lesion) prior to a subsequent test lesion increases the number of regenerating axons and accelerates the speed of regeneration from the test site. A major barrier to clinical translation is the lack of an ethically acceptable and clinically feasible method of conditioning that does not further damage the nerve. Conditioning electrical stimulation (CES), a non-injurious intervention, has previously been shown to improve neurite outgrowth in vitro. In this study, we examined whether CES upregulates regeneration-associated gene (RAG) expression and promotes nerve regeneration in vivo, similar to a traditional nerve crush conditioning lesion (CCL). Adult rats were divided into four cohorts based on conditioning treatment to the common peroneal (fibular) nerve: i) CES (1 h, 20 Hz); ii) CCL (10 s crush); iii) sham CES (1 h, 0 Hz); or iv) naive (unconditioned). Immunofluorescence and qRT-PCR revealed significant RAG upregulation in the dorsal root ganglia of both CES and CCL animals, evident at 3-14 days post-conditioning. To mimic a clinical microsurgical nerve repair, all cohorts underwent a common peroneal nerve cut and coaptation one week following conditioning. Both CES and CCL animals increased the length of nerve regeneration (3.8-fold) as well as the total number of regenerating axons (2.2-fold), compared to the sham and naive-conditioned animals (p < 0.001). These data support CES as a non-injurious conditioning paradigm that is comparable to a traditional CCL and is therefore a novel means to potentially enhance peripheral nerve repair in the clinical setting.

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