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Neuroskeletal Effects of Chronic Bioelectric Nerve Stimulation in Health and Diabetes
BACKGROUND/AIMS: Bioelectric nerve stimulation (eStim) is an emerging clinical paradigm that can promote nerve regeneration after trauma, including within the context of diabetes. However, its ability to prevent the onset of diabetic peripheral neuropathy (DPN) has not yet been evaluated. Beyond the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080454/ https://www.ncbi.nlm.nih.gov/pubmed/33935630 http://dx.doi.org/10.3389/fnins.2021.632768 |
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author | Beeve, Alec T. Shen, Ivana Zhang, Xiao Magee, Kristann Yan, Ying MacEwan, Matthew R. Scheller, Erica L. |
author_facet | Beeve, Alec T. Shen, Ivana Zhang, Xiao Magee, Kristann Yan, Ying MacEwan, Matthew R. Scheller, Erica L. |
author_sort | Beeve, Alec T. |
collection | PubMed |
description | BACKGROUND/AIMS: Bioelectric nerve stimulation (eStim) is an emerging clinical paradigm that can promote nerve regeneration after trauma, including within the context of diabetes. However, its ability to prevent the onset of diabetic peripheral neuropathy (DPN) has not yet been evaluated. Beyond the nerve itself, DPN has emerged as a potential contributor to sarcopenia and bone disease; thus, we hypothesized that eStim could serve as a strategy to simultaneously promote neural and musculoskeletal health in diabetes. METHODS: To address this question, an eStim paradigm pre-optimized to promote nerve regeneration was applied to the sciatic nerve, which directly innervates the tibia and lower limb, for 8 weeks in control and streptozotocin-induced type 1 diabetic (T1D) rats. Metabolic, gait, nerve and bone assessments were used to evaluate the progression of diabetes and the effect of sciatic nerve eStim on neuropathy and musculoskeletal disease, while also considering the effects of cuff placement and chronic eStim in otherwise healthy animals. RESULTS: Rats with T1D exhibited increased mechanical allodynia in the hindpaw, reduced muscle mass, decreased cortical and cancellous bone volume fraction (BVF), reduced cortical bone tissue mineral density (TMD), and decreased bone marrow adiposity. Type 1 diabetes also had an independent effect on gait. Placement of the cuff electrode alone resulted in altered gait patterns and unilateral reductions in tibia length, cortical BVF, and bone marrow adiposity. Alterations in gait patterns were restored by eStim and tibial lengthening was favored unilaterally; however, eStim did not prevent T1D-induced changes in muscle, bone, marrow adiposity or mechanical sensitivity. Beyond this, chronic eStim resulted in an independent, bilateral reduction in cortical TMD. CONCLUSION: Overall, these results provide new insight into the pathogenesis of diabetic neuroskeletal disease and its regulation by eStim. Though eStim did not prevent neural or musculoskeletal complications in T1D, our results demonstrate that clinical applications of peripheral neuromodulation ought to consider the impact of device placement and eStim on long-term skeletal health in both healthy individuals and those with metabolic disease. This includes monitoring for compounded bone loss to prevent unintended consequences including decreased bone mineral density and increased fracture risk. |
format | Online Article Text |
id | pubmed-8080454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80804542021-04-29 Neuroskeletal Effects of Chronic Bioelectric Nerve Stimulation in Health and Diabetes Beeve, Alec T. Shen, Ivana Zhang, Xiao Magee, Kristann Yan, Ying MacEwan, Matthew R. Scheller, Erica L. Front Neurosci Neuroscience BACKGROUND/AIMS: Bioelectric nerve stimulation (eStim) is an emerging clinical paradigm that can promote nerve regeneration after trauma, including within the context of diabetes. However, its ability to prevent the onset of diabetic peripheral neuropathy (DPN) has not yet been evaluated. Beyond the nerve itself, DPN has emerged as a potential contributor to sarcopenia and bone disease; thus, we hypothesized that eStim could serve as a strategy to simultaneously promote neural and musculoskeletal health in diabetes. METHODS: To address this question, an eStim paradigm pre-optimized to promote nerve regeneration was applied to the sciatic nerve, which directly innervates the tibia and lower limb, for 8 weeks in control and streptozotocin-induced type 1 diabetic (T1D) rats. Metabolic, gait, nerve and bone assessments were used to evaluate the progression of diabetes and the effect of sciatic nerve eStim on neuropathy and musculoskeletal disease, while also considering the effects of cuff placement and chronic eStim in otherwise healthy animals. RESULTS: Rats with T1D exhibited increased mechanical allodynia in the hindpaw, reduced muscle mass, decreased cortical and cancellous bone volume fraction (BVF), reduced cortical bone tissue mineral density (TMD), and decreased bone marrow adiposity. Type 1 diabetes also had an independent effect on gait. Placement of the cuff electrode alone resulted in altered gait patterns and unilateral reductions in tibia length, cortical BVF, and bone marrow adiposity. Alterations in gait patterns were restored by eStim and tibial lengthening was favored unilaterally; however, eStim did not prevent T1D-induced changes in muscle, bone, marrow adiposity or mechanical sensitivity. Beyond this, chronic eStim resulted in an independent, bilateral reduction in cortical TMD. CONCLUSION: Overall, these results provide new insight into the pathogenesis of diabetic neuroskeletal disease and its regulation by eStim. Though eStim did not prevent neural or musculoskeletal complications in T1D, our results demonstrate that clinical applications of peripheral neuromodulation ought to consider the impact of device placement and eStim on long-term skeletal health in both healthy individuals and those with metabolic disease. This includes monitoring for compounded bone loss to prevent unintended consequences including decreased bone mineral density and increased fracture risk. Frontiers Media S.A. 2021-04-07 /pmc/articles/PMC8080454/ /pubmed/33935630 http://dx.doi.org/10.3389/fnins.2021.632768 Text en Copyright © 2021 Beeve, Shen, Zhang, Magee, Yan, MacEwan and Scheller. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Beeve, Alec T. Shen, Ivana Zhang, Xiao Magee, Kristann Yan, Ying MacEwan, Matthew R. Scheller, Erica L. Neuroskeletal Effects of Chronic Bioelectric Nerve Stimulation in Health and Diabetes |
title | Neuroskeletal Effects of Chronic Bioelectric Nerve Stimulation in Health and Diabetes |
title_full | Neuroskeletal Effects of Chronic Bioelectric Nerve Stimulation in Health and Diabetes |
title_fullStr | Neuroskeletal Effects of Chronic Bioelectric Nerve Stimulation in Health and Diabetes |
title_full_unstemmed | Neuroskeletal Effects of Chronic Bioelectric Nerve Stimulation in Health and Diabetes |
title_short | Neuroskeletal Effects of Chronic Bioelectric Nerve Stimulation in Health and Diabetes |
title_sort | neuroskeletal effects of chronic bioelectric nerve stimulation in health and diabetes |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080454/ https://www.ncbi.nlm.nih.gov/pubmed/33935630 http://dx.doi.org/10.3389/fnins.2021.632768 |
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