Literature DB >> 1559923

Metabolic adaptations to training precede changes in muscle mitochondrial capacity.

H J Green1, R Helyar, M Ball-Burnett, N Kowalchuk, S Symon, B Farrance.   

Abstract

To determine whether increases in muscle mitochondrial capacity are necessary for the characteristic lower exercise glycogen loss and lactate concentration observed during exercise in the trained state, we have employed a short-term training model involving 2 h of cycling per day at 67% maximal O2 uptake (VO2max) for 5-7 consecutive days. Before and after training, biopsies were extracted from the vastus lateralis of nine male subjects during a continuous exercise challenge consisting of 30 min of work at 67% VO2max followed by 30 min at 76% VO2max. Analysis of samples at 0, 15, 20, and 60 min indicated a pronounced reduction (P less than 0.05) in glycogen utilization after training. Reductions in glycogen utilization were accompanied by reductions (P less than 0.05) in muscle lactate concentration (mmol/kg dry wt) at 15 min [37.4 +/- 9.3 (SE) vs. 20.2 +/- 5.3], 30 min (30.5 +/- 6.9 vs. 17.6 +/- 3.8), and 60 min (26.5 +/- 5.8 vs. 17.8 +/- 3.5) of exercise. Maximal aerobic power, VO2max (l/min) was unaffected by the training (3.99 +/- 0.21 vs. 4.05 +/- 0.26). Measurements of maximal activities of enzymes representative of the citric acid cycle (succinic dehydrogenase and citrate synthase) were similar before and after the training. It is concluded that, in the voluntary exercising human, altered metabolic events are an early adaptive response to training and need not be accompanied by changes in muscle mitochondrial capacity.

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Year:  1992        PMID: 1559923     DOI: 10.1152/jappl.1992.72.2.484

Source DB:  PubMed          Journal:  J Appl Physiol (1985)        ISSN: 0161-7567


  33 in total

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Review 2.  Training techniques to improve endurance exercise performances.

Authors:  Zuko N Kubukeli; Timothy D Noakes; Steven C Dennis
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4.  Effects of aerobic training on pyruvate dehydrogenase and pyruvate dehydrogenase kinase in human skeletal muscle.

Authors:  Paul J LeBlanc; Sandra J Peters; Rebecca J Tunstall; David Cameron-Smith; George J F Heigenhauser
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5.  Adaptations in muscle metabolic regulation require only a small dose of aerobic-based exercise.

Authors:  Howard J Green; Margaret Burnett; Ira Jacobs; Don Ranney; Ian Smith; Susan Tupling
Journal:  Eur J Appl Physiol       Date:  2012-06-17       Impact factor: 3.078

6.  PGC-1α mediates a rapid, exercise-induced downregulation of glycogenolysis in rat skeletal muscle.

Authors:  Sang Hyun Kim; Jin Ho Koh; Kazuhiko Higashida; Su Ryun Jung; John O Holloszy; Dong-Ho Han
Journal:  J Physiol       Date:  2014-12-23       Impact factor: 5.182

Review 7.  Training-Induced Changes in Mitochondrial Content and Respiratory Function in Human Skeletal Muscle.

Authors:  Cesare Granata; Nicholas A Jamnick; David J Bishop
Journal:  Sports Med       Date:  2018-08       Impact factor: 11.136

Review 8.  Control of Muscle Metabolism by the Mediator Complex.

Authors:  Leonela Amoasii; Eric N Olson; Rhonda Bassel-Duby
Journal:  Cold Spring Harb Perspect Med       Date:  2018-02-01       Impact factor: 6.915

9.  High-intensity interval training increases in vivo oxidative capacity with no effect on P(i)→ATP rate in resting human muscle.

Authors:  Ryan G Larsen; Douglas E Befroy; Jane A Kent-Braun
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2012-12-19       Impact factor: 3.619

10.  Short-term training alters the control of mitochondrial respiration rate before maximal oxidative ATP synthesis.

Authors:  G Layec; L J Haseler; J Hoff; C R Hart; X Liu; Y Le Fur; E-K Jeong; R S Richardson
Journal:  Acta Physiol (Oxf)       Date:  2013-05-02       Impact factor: 6.311

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