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GDNF content and NMJ morphology are altered in recruited muscles following high‐speed and resistance wheel training

Glial cell line‐derived neurotrophic factor (GDNF) may play a role in delaying the onset of aging and help compress morbidity by preventing motor unit degeneration. Exercise has been shown to alter GDNF expression differently in slow‐ and fast‐twitch myofibers. The aim was to examine the effects of...

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Autores principales: Gyorkos, Amy Morrison, Spitsbergen, John M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966253/
https://www.ncbi.nlm.nih.gov/pubmed/24744904
http://dx.doi.org/10.1002/phy2.235
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author Gyorkos, Amy Morrison
Spitsbergen, John M.
author_facet Gyorkos, Amy Morrison
Spitsbergen, John M.
author_sort Gyorkos, Amy Morrison
collection PubMed
description Glial cell line‐derived neurotrophic factor (GDNF) may play a role in delaying the onset of aging and help compress morbidity by preventing motor unit degeneration. Exercise has been shown to alter GDNF expression differently in slow‐ and fast‐twitch myofibers. The aim was to examine the effects of different intensities (10, 20, ~30, and ~40 m·min(−1)) of wheel running on GDNF expression and neuromuscular junction (NMJ) plasticity in slow‐ and fast‐twitch myofibers. Male Sprague‐Dawley Rats (4 weeks old) were divided into two sedentary control groups (CON4 week, n = 5 and CON6 week, n = 5), two involuntary running groups, one at a low velocity; 10 m/min (INVOL‐low, n = 5), and one at a higher velocity; 20 m/min (INVOL‐high, n = 5), and two voluntary running groups with resistance (VOL‐R, n = 5, 120 g), and without resistance (VOL‐NR, n = 5, 4.5 g). GDNF protein content, determined by enzyme‐linked immunosorbent assay (ELISA), increased significantly in the recruited muscles. Plantaris (PLA) GDNF protein content increased 174% (P <0.05) and 161% (P <0.05) and end plate‐stained area increased 123% (P <0.05) and 72% (P <0.05) following VOL‐R, and VOL‐NR training, respectively, when compared to age‐matched controls. A relationship exists between GDNF protein content and end plate area (r = 0.880, P < 0.01, n = 15). VOL‐R training also resulted in more dispersed synapses in the PLA muscle when compared to age‐matched controls (P <0.05). Higher intensity exercise (>30 m/min) can increase GDNF protein content in fast‐twitch myofibers as well as induce changes in the NMJ morphology. These findings help to inform exercise prescription to preserve the integrity of the neuromuscular system through aging and disease.
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spelling pubmed-39662532014-03-31 GDNF content and NMJ morphology are altered in recruited muscles following high‐speed and resistance wheel training Gyorkos, Amy Morrison Spitsbergen, John M. Physiol Rep Original Research Glial cell line‐derived neurotrophic factor (GDNF) may play a role in delaying the onset of aging and help compress morbidity by preventing motor unit degeneration. Exercise has been shown to alter GDNF expression differently in slow‐ and fast‐twitch myofibers. The aim was to examine the effects of different intensities (10, 20, ~30, and ~40 m·min(−1)) of wheel running on GDNF expression and neuromuscular junction (NMJ) plasticity in slow‐ and fast‐twitch myofibers. Male Sprague‐Dawley Rats (4 weeks old) were divided into two sedentary control groups (CON4 week, n = 5 and CON6 week, n = 5), two involuntary running groups, one at a low velocity; 10 m/min (INVOL‐low, n = 5), and one at a higher velocity; 20 m/min (INVOL‐high, n = 5), and two voluntary running groups with resistance (VOL‐R, n = 5, 120 g), and without resistance (VOL‐NR, n = 5, 4.5 g). GDNF protein content, determined by enzyme‐linked immunosorbent assay (ELISA), increased significantly in the recruited muscles. Plantaris (PLA) GDNF protein content increased 174% (P <0.05) and 161% (P <0.05) and end plate‐stained area increased 123% (P <0.05) and 72% (P <0.05) following VOL‐R, and VOL‐NR training, respectively, when compared to age‐matched controls. A relationship exists between GDNF protein content and end plate area (r = 0.880, P < 0.01, n = 15). VOL‐R training also resulted in more dispersed synapses in the PLA muscle when compared to age‐matched controls (P <0.05). Higher intensity exercise (>30 m/min) can increase GDNF protein content in fast‐twitch myofibers as well as induce changes in the NMJ morphology. These findings help to inform exercise prescription to preserve the integrity of the neuromuscular system through aging and disease. Wiley Periodicals, Inc. 2014-02-25 /pmc/articles/PMC3966253/ /pubmed/24744904 http://dx.doi.org/10.1002/phy2.235 Text en © 2014 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Gyorkos, Amy Morrison
Spitsbergen, John M.
GDNF content and NMJ morphology are altered in recruited muscles following high‐speed and resistance wheel training
title GDNF content and NMJ morphology are altered in recruited muscles following high‐speed and resistance wheel training
title_full GDNF content and NMJ morphology are altered in recruited muscles following high‐speed and resistance wheel training
title_fullStr GDNF content and NMJ morphology are altered in recruited muscles following high‐speed and resistance wheel training
title_full_unstemmed GDNF content and NMJ morphology are altered in recruited muscles following high‐speed and resistance wheel training
title_short GDNF content and NMJ morphology are altered in recruited muscles following high‐speed and resistance wheel training
title_sort gdnf content and nmj morphology are altered in recruited muscles following high‐speed and resistance wheel training
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966253/
https://www.ncbi.nlm.nih.gov/pubmed/24744904
http://dx.doi.org/10.1002/phy2.235
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