神经肌肉传递和Na+通道抑制剂对离体慢速和快速抽搐肌肉力量-持续时间关系的影响。

IF 1.7 3区 生物学 Q4 CELL BIOLOGY
Mari S Matsumoto, Taku Hamada, Daiki Watanabe
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引用次数: 0

摘要

力量-持续时间(S-D)关系反映了肌肉的兴奋性,这部分决定了力量的产生。离体肌肉中含有部分神经和神经肌肉连接,表明肌肉兴奋不仅启动肌肉膜,还启动神经末梢,从而启动神经肌肉传递(NMT)。本研究旨在探讨抑制神经肌肉传递对小鼠慢肌和快肌S-D关系的影响。电刺激孤立的慢抽动比目鱼肌(SOL)和快抽动指长伸肌(EDL),并在不同持续时间内确定产生力所需的最小场强[阈值场强(ThFS)]。在SOL和EDL肌肉中存在包括泮库溴铵(Pan)和琥珀酰胆碱在内的NMT抑制剂时,ThFS显著增加。此外,与EDL相比,NMT抑制剂存在时,SOL中的ThFS更高。为了阐明溶胶和EDL之间不同ThFS的机制,研究了Na+通道的贡献。在1 μM Pan存在的情况下,河蟹毒素对Na+通道的部分抑制消除了EDL和SOL之间ThFS的差异。这些结果表明(1)NMT显著增强了肌肉的兴奋性,(2)NMT不存在时,快肌的动作电位阈值高于慢肌,(3)Na+通道可能是慢肌和快肌之间差异的原因之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of neuromuscular transmission and Na+ channel inhibitors on strength-duration relationship in isolated slow- and fast-twitch muscles.

Strength-duration (S-D) relationship reflects muscle excitability which partially determines force production. Isolated muscle contains part of nerve and neuromuscular junction, suggesting that muscle excitation initiates not only muscle membrane but also nerve terminals and hence neuromuscular transmission (NMT). This study aimed to examine the effects of inhibition of neuromuscular transmission on S-D relationship in slow- and fast-twitch muscles of mice. Isolated slow-twitch soleus (SOL) and fast-twitch extensor digitorum longus (EDL) muscles were electrically stimulated, and minimal field strength required for force generation [threshold field strength (ThFS)] was determined at various duration. ThFS significantly increased in the presence of NMT inhibitors including pancuronium (Pan) and succinylcholine in both SOL and EDL muscles. Moreover, ThFS in the presence of NMT inhibitors was higher in SOL compared to EDL. To clarify the mechanism of the different ThFS between SOL and EDL, contribution of Na+ channel was investigated. In the presence of 1 μM Pan, partial inhibition of Na+ channel by tetrodotoxin eliminated the difference in ThFS between EDL and SOL. These results suggest that (1) NMT significantly enhances muscle excitability, (2) threshold of action potential in fast-twitch muscle is greater compared with slow-twitch muscle if no existence of NMT, and (3) Na+ channel likely contribute to the difference between slow- and fast-twitch muscles.

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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
21
审稿时长
>12 weeks
期刊介绍: The Journal of Muscle Research and Cell Motility has as its main aim the publication of original research which bears on either the excitation and contraction of muscle, the analysis of any one of the processes involved therein, the processes underlying contractility and motility of animal and plant cells, the toxicology and pharmacology related to contractility, or the formation, dynamics and turnover of contractile structures in muscle and non-muscle cells. Studies describing the impact of pathogenic mutations in genes encoding components of contractile structures in humans or animals are welcome, provided they offer mechanistic insight into the disease process or the underlying gene function. The policy of the Journal is to encourage any form of novel practical study whatever its specialist interest, as long as it falls within this broad field. Theoretical essays are welcome provided that they are concise and suggest practical ways in which they may be tested. Manuscripts reporting new mutations in known disease genes without validation and mechanistic insight will not be considered. It is the policy of the journal that cells lines, hybridomas and DNA clones should be made available by the developers to any qualified investigator. Submission of a manuscript for publication constitutes an agreement of the authors to abide by this principle.
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