不同骨骼肌和肌纤维的能量代谢:对损伤和膳食补充的影响。

IF 2.9 4区 医学 Q2 PHYSIOLOGY
Andrey V Kuznetsov, Raimund Margreiter, Judith Hagenbuchner, Michael J Ausserlechner
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引用次数: 0

摘要

骨骼肌所需的能量供应是基于糖酵解或线粒体氧化磷酸化(OxPhos)。这两种生物能量途径是平衡互补的。糖酵解比OxPhos更快,而OxPhos效率更高。这两种途径的一个共同特征是高能磷酸盐的区隔及其代谢通道。糖酵解肌更宽,而氧化肌有更多的线粒体。重要的是,氧化(慢抽搐)与糖酵解(快抽搐)肌肉和肌纤维的生物能量机制有显著差异。其优点是,最佳的纤维多样性可以提供最佳的肌肉功能。各种肌酸激酶异构体和磷酸肌酸在糖酵解和氧化肌肉能量代谢中起重要作用,但它们的作用因肌肉类型而异。在糖酵解肌肉中,磷酸肌酸由肌酸和ATP通过胞质肌酸激酶产生,通常被认为是快速递送ATP的细胞能量储存,而在氧化肌肉中,磷酸肌酸和线粒体肌酸激酶是细胞内能量运输的主要参与者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Energy metabolism in different skeletal muscles and muscle fibers: implications for injury and dietary supplementation.

The necessary energy supply in skeletal muscles is based on either glycolysis or mitochondrial oxidative phosphorylation (OxPhos). These two bioenergetic pathways are in balanced complementation. Glycolysis is faster than OxPhos, whereas OxPhos is much more efficient. One common feature of both pathways is the compartmentation of high-energy phosphates and their metabolic channeling. The glycolytic muscles are wider, whereas oxidative muscles have significantly more mitochondria. Importantly, a striking difference in bioenergetic mechanisms in oxidative (slow-twitch) versus glycolytic (fast-twitch) muscles and muscle fibers has been clearly shown. The advantage is that the optimal fiber diversity can provide the best muscle function. Various creatine kinase isoforms and phosphocreatine play an important role in glycolytic and oxidative muscles energy metabolism, but their roles are very different, depending on the muscle type. In the glycolytic muscles, phosphocreatine, produced from creatine and ATP by cytosolic creatine kinase, is mostly considered a cellular energy store for fast ATP delivery, whereas in the oxidative muscles, phosphocreatine and mitochondrial creatine kinase are the main players in the intracellular energy transport.

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来源期刊
CiteScore
8.80
自引率
2.20%
发文量
121
审稿时长
4-8 weeks
期刊介绍: Pflügers Archiv European Journal of Physiology publishes those results of original research that are seen as advancing the physiological sciences, especially those providing mechanistic insights into physiological functions at the molecular and cellular level, and clearly conveying a physiological message. Submissions are encouraged that deal with the evaluation of molecular and cellular mechanisms of disease, ideally resulting in translational research. Purely descriptive papers covering applied physiology or clinical papers will be excluded. Papers on methodological topics will be considered if they contribute to the development of novel tools for further investigation of (patho)physiological mechanisms.
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