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Modelling Skeletal Muscle Motor Unit Recruitment Contributions to Contractile Function: Part 3 - Substrate Oxidation of Phosphagen, Lipid, and Carbohydrate Metabolism

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F44555601%3A13450%2F24%3A43899206" target="_blank" >RIV/44555601:13450/24:43899206 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.qeios.com/read/C0I8U0.2" target="_blank" >https://www.qeios.com/read/C0I8U0.2</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.32388/C0I8U0.2" target="_blank" >10.32388/C0I8U0.2</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Modelling Skeletal Muscle Motor Unit Recruitment Contributions to Contractile Function: Part 3 - Substrate Oxidation of Phosphagen, Lipid, and Carbohydrate Metabolism

  • Original language description

    This study aimed to apply and expand a prior model of motor unit recruitment of the vastus lateralis muscle (VL) to explore theoretical motor unit-specific substrate oxidation. The model utilized repeated contractions of varied frequency and fraction of motor unit recruitment, and four different genetic expressions of motor unit proportions. The study applied prior modelled data of the vastus lateralis (VL) motor unit contractile power and turnover of adenosine triphosphate (ATPto) based on non-linear functions of estimated percentage contributions of different energy systems across various muscle fibre types and contraction frequencies. Using LabVIEW? programming, the model then used the prior data of ATPto and known ATPto coefficients for substrate oxidation for the energy systems of phosphagen, glycolytic, and mitochondrial respiration from fatty acid and carbohydrate to calculate total and fibre type (motor unit) specific creatine phosphate catabolism, glycogenolysis, glycolytic glucose oxidation, fatty acid oxidation in mitochondrial respiration, glucose oxidation in mitochondrial respiration, and lactate production. Results revealed that for the phosphagen system, substrate turnover was far larger than research-based expressions of decreasing concentrations of creatine phosphate and ATP. This is to be expected for modelled research involving temporal summation of metabolism. Creatine phosphate is continually broken down and partially replenished during low-intensity exercise, with such partial replenishment sustained during more intense exercise thanks to the creatine kinase shuttle. For carbohydrate oxidation, mitochondrial respiration accounted for the greatest substrate oxidation in type I and I-IIa motor units, where glycolysis accounted for most substrate oxidation in type IIa, IIab, and IIb motor units. Fatty acid oxidation was larger for lower motor unit recruitment conditions and highest for type I-IIa and IIa motor units. This result is logical based on the larger net muscle fibre recruitment for contraction conditions necessitating progression to fast twitch motor units, causing higher substrate oxidation. Such findings reinforce the need for more research on fibre type-specific substrate oxidation during different exercise intensities and durations.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>ost</sub> - Miscellaneous article in a specialist periodical

  • CEP classification

  • OECD FORD branch

    30105 - Physiology (including cytology)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Qeios

  • ISSN

    2632-3834

  • e-ISSN

    2632-3834

  • Volume of the periodical

    2024

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    19

  • Pages from-to

    1-19

  • UT code for WoS article

  • EID of the result in the Scopus database