Forelimb Resistance Exercise Protects Against Neuromuscular Junction Denervation in the SOD1-G93A Rat Model of ALS.

Degenerative Neurological and Neuromuscular Disease Pub Date : 2022-11-22 eCollection Date: 2022-01-01 DOI:10.2147/DNND.S388455
Hiroshi Nishimune, Kimberly G Stanford, Jie Chen, James D Odum, Alexander D Rorie, Robert S Rogers, Joshua L Wheatley, Paige C Geiger, John A Stanford
{"title":"Forelimb Resistance Exercise Protects Against Neuromuscular Junction Denervation in the SOD1-G93A Rat Model of ALS.","authors":"Hiroshi Nishimune,&nbsp;Kimberly G Stanford,&nbsp;Jie Chen,&nbsp;James D Odum,&nbsp;Alexander D Rorie,&nbsp;Robert S Rogers,&nbsp;Joshua L Wheatley,&nbsp;Paige C Geiger,&nbsp;John A Stanford","doi":"10.2147/DNND.S388455","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>The symptoms of Amyotrophic Lateral Sclerosis (ALS) include muscle weakness and eventual paralysis. These symptoms result from denervation of the neuromuscular junction (NMJ) and motor neuron cell death in the brain and spinal cord. Due to the \"dying back\" pattern of motor neuron degeneration, protecting NMJs should be a therapeutic priority. Although exercise has the potential to protect against NMJ denervation, its use in ALS has been controversial. Most preclinical studies have focused on aerobic exercise, which report that exercise can be beneficial at moderate intensities. The effects of resistance exercise on NMJ preservation in limb muscles have not been explored.</p><p><strong>Methods: </strong>We trained male SOD1-G93A rats, which model ALS, to perform a unilateral isometric forelimb resistance exercise task. This task allows within-animal comparisons of trained and untrained forelimbs. We then determined the effects of isometric resistance exercise on NMJ denervation and AMP kinase (AMPK) activation in forelimb muscles.</p><p><strong>Results: </strong>Our results revealed that SOD1-G93A rats were able to learn and perform the task similarly to wildtype rats, even after loss of body weight. SOD1-G93A rats exhibited significantly greater NMJ innervation in their trained vs their untrained forelimb biceps muscles. Measures of activated (phosphorylated) AMPK (pAMPK) were also greater in the trained vs untrained forelimb triceps muscles.</p><p><strong>Discussion: </strong>These results demonstrate that isometric resistance exercise may protect against NMJ denervation in ALS. Future studies are required to determine the extent to which our findings generalize to female SOD1-G93A rats and to other subtypes of ALS.</p>","PeriodicalId":11147,"journal":{"name":"Degenerative Neurological and Neuromuscular Disease","volume":" ","pages":"145-155"},"PeriodicalIF":0.0000,"publicationDate":"2022-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/89/6d/dnnd-12-145.PMC9700444.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Degenerative Neurological and Neuromuscular Disease","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/DNND.S388455","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: The symptoms of Amyotrophic Lateral Sclerosis (ALS) include muscle weakness and eventual paralysis. These symptoms result from denervation of the neuromuscular junction (NMJ) and motor neuron cell death in the brain and spinal cord. Due to the "dying back" pattern of motor neuron degeneration, protecting NMJs should be a therapeutic priority. Although exercise has the potential to protect against NMJ denervation, its use in ALS has been controversial. Most preclinical studies have focused on aerobic exercise, which report that exercise can be beneficial at moderate intensities. The effects of resistance exercise on NMJ preservation in limb muscles have not been explored.

Methods: We trained male SOD1-G93A rats, which model ALS, to perform a unilateral isometric forelimb resistance exercise task. This task allows within-animal comparisons of trained and untrained forelimbs. We then determined the effects of isometric resistance exercise on NMJ denervation and AMP kinase (AMPK) activation in forelimb muscles.

Results: Our results revealed that SOD1-G93A rats were able to learn and perform the task similarly to wildtype rats, even after loss of body weight. SOD1-G93A rats exhibited significantly greater NMJ innervation in their trained vs their untrained forelimb biceps muscles. Measures of activated (phosphorylated) AMPK (pAMPK) were also greater in the trained vs untrained forelimb triceps muscles.

Discussion: These results demonstrate that isometric resistance exercise may protect against NMJ denervation in ALS. Future studies are required to determine the extent to which our findings generalize to female SOD1-G93A rats and to other subtypes of ALS.

Abstract Image

Abstract Image

Abstract Image

前肢阻力运动对SOD1-G93A肌萎缩侧索硬化症大鼠神经肌肉连接处失神经的保护作用。
简介:肌萎缩性侧索硬化症(ALS)的症状包括肌肉无力和最终瘫痪。这些症状是由神经肌肉连接处(NMJ)的失神经支配和脑和脊髓的运动神经元细胞死亡引起的。由于运动神经元退化的“死后”模式,保护NMJs应该是治疗的优先事项。尽管运动有可能防止NMJ失神经支配,但它在ALS中的应用一直存在争议。大多数临床前研究都集中在有氧运动上,这些研究报告称,中等强度的运动是有益的。阻力运动对肢体肌肉NMJ保存的影响尚未被研究。方法:对雄性SOD1-G93A大鼠进行单侧等长前肢阻力训练。这项任务允许在动物内部比较训练和未训练的前肢。然后,我们确定了等长阻力运动对前肢肌肉NMJ去神经支配和AMP激酶(AMPK)激活的影响。结果:我们的研究结果显示,即使在体重减轻后,SOD1-G93A大鼠的学习和执行任务的能力与野生型大鼠相似。SOD1-G93A大鼠训练后的前肢二头肌的NMJ神经支配明显大于未训练的大鼠。激活的(磷酸化的)AMPK (pAMPK)在训练的前肢三头肌中也比未训练的大。讨论:这些结果表明,等长阻力运动可以防止肌萎缩侧索硬化症的NMJ失神经支配。未来的研究需要确定我们的发现在多大程度上推广到雌性SOD1-G93A大鼠和其他ALS亚型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信