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Direct electrical stimulation impacts on neuromuscular junction morphology on both stimulated and unstimulated contralateral soleus
BACKGROUND: There is increasing evidence of crosstalk between organs. The neuromuscular junction (NMJ) is a peripheral chemical synapse whose function and morphology are sensitive to acetylcholine (ACh) release and muscle depolarization. In an attempt to improve our understanding of NMJ plasticity a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235881/ https://www.ncbi.nlm.nih.gov/pubmed/37060275 http://dx.doi.org/10.1002/jcsm.13235 |
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author | Lee, Young il Cacciani, Nicola Wen, Ya Zhang, Xiang Hedström, Yvette Thompson, Wesley Larsson, Lars |
author_facet | Lee, Young il Cacciani, Nicola Wen, Ya Zhang, Xiang Hedström, Yvette Thompson, Wesley Larsson, Lars |
author_sort | Lee, Young il |
collection | PubMed |
description | BACKGROUND: There is increasing evidence of crosstalk between organs. The neuromuscular junction (NMJ) is a peripheral chemical synapse whose function and morphology are sensitive to acetylcholine (ACh) release and muscle depolarization. In an attempt to improve our understanding of NMJ plasticity and muscle crosstalk, the effects of unilateral direct electrical stimulation of a hindlimb muscle on the NMJ were investigated in rats exposed long‐term post‐synaptic neuromuscular blockade. METHODS: Sprague Dawley rats were subjected to post‐synaptic blockade of neuromuscular transmission by systemic administration of α‐cobrotoxin and mechanically ventilated for up to 8 days and compared with untreated sham operated controls and animals exposed to unilateral chronic electrical stimulation 12 h/day for 5 or 8 days. RESULTS: NMJs produced axonal and glial sprouts (growth of processes that extend beyond the confines of the synapse defined by high‐density aggregates of acetylcholine receptors [AChRs]) in response to post‐synaptic neuromuscular blockade, but less than reported after peripheral denervation or pre‐synaptic blockade. Direct electrical soleus muscle stimulation reduced the terminal Schwann cell (tSC) and axonal sprouting in both stimulated and non‐stimulated contralateral soleus. Eight days chronic stimulation reduced (P < 0.001) the number of tSC sprouts on stimulated and non‐stimulated soleus from 6.7 ± 0.5 and 6.9 ± 0.5 sprouts per NMJ, respectively, compared with 10.3 ± 0.9 tSC per NMJ (P < 0.001) in non‐stimulated soleus from rats immobilized for 8 days. A similar reduction of axonal sprouts (P < 0.001) was observed in stimulated and non‐stimulated contralateral soleus in response to chronic electrical stimulation. RNAseq‐based gene expression analyses confirmed a restoring effect on both stimulated and unstimulated contralateral muscle. The cross‐over effect was paralleled by increased cytokine/chemokine levels in stimulated and contralateral unstimulated muscle as well as in plasma. CONCLUSIONS: Motor axon terminals and terminal Schwann cells at NMJs of rats subjected to post‐synaptic neuromuscular blockade exhibited sprouting responses. These axonal and glial responses were likely dampened by a muscle‐derived myokines released in an activity‐dependent manner with both local and systemic effects. |
format | Online Article Text |
id | pubmed-10235881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102358812023-06-03 Direct electrical stimulation impacts on neuromuscular junction morphology on both stimulated and unstimulated contralateral soleus Lee, Young il Cacciani, Nicola Wen, Ya Zhang, Xiang Hedström, Yvette Thompson, Wesley Larsson, Lars J Cachexia Sarcopenia Muscle Original Articles BACKGROUND: There is increasing evidence of crosstalk between organs. The neuromuscular junction (NMJ) is a peripheral chemical synapse whose function and morphology are sensitive to acetylcholine (ACh) release and muscle depolarization. In an attempt to improve our understanding of NMJ plasticity and muscle crosstalk, the effects of unilateral direct electrical stimulation of a hindlimb muscle on the NMJ were investigated in rats exposed long‐term post‐synaptic neuromuscular blockade. METHODS: Sprague Dawley rats were subjected to post‐synaptic blockade of neuromuscular transmission by systemic administration of α‐cobrotoxin and mechanically ventilated for up to 8 days and compared with untreated sham operated controls and animals exposed to unilateral chronic electrical stimulation 12 h/day for 5 or 8 days. RESULTS: NMJs produced axonal and glial sprouts (growth of processes that extend beyond the confines of the synapse defined by high‐density aggregates of acetylcholine receptors [AChRs]) in response to post‐synaptic neuromuscular blockade, but less than reported after peripheral denervation or pre‐synaptic blockade. Direct electrical soleus muscle stimulation reduced the terminal Schwann cell (tSC) and axonal sprouting in both stimulated and non‐stimulated contralateral soleus. Eight days chronic stimulation reduced (P < 0.001) the number of tSC sprouts on stimulated and non‐stimulated soleus from 6.7 ± 0.5 and 6.9 ± 0.5 sprouts per NMJ, respectively, compared with 10.3 ± 0.9 tSC per NMJ (P < 0.001) in non‐stimulated soleus from rats immobilized for 8 days. A similar reduction of axonal sprouts (P < 0.001) was observed in stimulated and non‐stimulated contralateral soleus in response to chronic electrical stimulation. RNAseq‐based gene expression analyses confirmed a restoring effect on both stimulated and unstimulated contralateral muscle. The cross‐over effect was paralleled by increased cytokine/chemokine levels in stimulated and contralateral unstimulated muscle as well as in plasma. CONCLUSIONS: Motor axon terminals and terminal Schwann cells at NMJs of rats subjected to post‐synaptic neuromuscular blockade exhibited sprouting responses. These axonal and glial responses were likely dampened by a muscle‐derived myokines released in an activity‐dependent manner with both local and systemic effects. John Wiley and Sons Inc. 2023-04-15 /pmc/articles/PMC10235881/ /pubmed/37060275 http://dx.doi.org/10.1002/jcsm.13235 Text en © 2023 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Lee, Young il Cacciani, Nicola Wen, Ya Zhang, Xiang Hedström, Yvette Thompson, Wesley Larsson, Lars Direct electrical stimulation impacts on neuromuscular junction morphology on both stimulated and unstimulated contralateral soleus |
title | Direct electrical stimulation impacts on neuromuscular junction morphology on both stimulated and unstimulated contralateral soleus |
title_full | Direct electrical stimulation impacts on neuromuscular junction morphology on both stimulated and unstimulated contralateral soleus |
title_fullStr | Direct electrical stimulation impacts on neuromuscular junction morphology on both stimulated and unstimulated contralateral soleus |
title_full_unstemmed | Direct electrical stimulation impacts on neuromuscular junction morphology on both stimulated and unstimulated contralateral soleus |
title_short | Direct electrical stimulation impacts on neuromuscular junction morphology on both stimulated and unstimulated contralateral soleus |
title_sort | direct electrical stimulation impacts on neuromuscular junction morphology on both stimulated and unstimulated contralateral soleus |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235881/ https://www.ncbi.nlm.nih.gov/pubmed/37060275 http://dx.doi.org/10.1002/jcsm.13235 |
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