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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...

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Autores principales: Lee, Young il, Cacciani, Nicola, Wen, Ya, Zhang, Xiang, Hedström, Yvette, Thompson, Wesley, Larsson, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
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.
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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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