Journal Article Ppublish 1 citation
PubMed: 40285367 DOI: 10.1002/jcsm.13775
Mitochondrial Sensitivity to Submaximal [ADP] Following Bed Rest: A Novel Two-Phase Approach Associated With Fibre Types.
J Cachexia Sarcopenia Muscle 16(3):e13775
Authors: Lucrezia Zuccarelli, Maria De Martino, Antonio Filippi, Alice E Knapton, Benjamin D Thackray, Giovanni Baldassarre, Boštjan Šimunič, Rado Pišot, Giuseppe Sirago, Elena Monti, Marco Narici, Miriam Isola, Andrew J Murray, Giovanna Lippe, Bruno Grassi
Affiliations
- Department of Medicine, University of Udine, Udine, Italy.
- Department of Physiology, Neuroscience and Development, University of Cambridge, Cambridge, UK.
- Institute of Kinesiology Research, Science and Research Centre, Koper, Slovenia.
- Department of Biomedical Sciences, University of Padova, Padova, Italy.
- Institute of Sport Sciences and Department of Biomedical Sciences, University of Lausanne, Lausanne, Switzerland.
Abstract
BACKGROUND
We recently demonstrated that following a 10-day exposure to inactivity/simulated microgravity impairments of oxidative metabolism were located 'upstream' of mitochondrial function, as evaluated by maximal ADP-stimulated mitochondrial respiration (JO) determined ex vivo. The aim of this study was to evaluate mitochondrial sensitivity to submaximal [ADP] by an alternative approach aimed at identifying responses associated with fibre type composition.
METHODS
Isolated permeabilized vastus lateralis fibres were analysed by high-resolution respirometry in 9 young males before and after a 10-day horizontal bed rest. Eleven submaximal titrations of ADP (from 12.5 to 10 000 μM) were utilized to assess complex I + II-linked ADP sensitivity. We applied to JO versus [ADP] data a traditional Michaelis-Menten kinetics equation, with the calculation of the apparent K and maximal respiration (V), and two 'sequential' hyperbolic equations, yielding two K and V values. The two-hyperbolic equations were solved and the [ADP] value corresponding to 50% of JO was calculated. Isoform expression of myosin heavy chains (MyHC) 1, 2A and 2X was also determined. Control experiments were also carried out on rat skeletal muscle samples with different percentages of MyHC isoforms.
RESULTS
The two hyperbolic equations provided an alternative fitting of data and identified two distinct phases of the JO versus [ADP] response: a first phase characterized by low V (V, 28 ± 10 pmol s mg) and apparent K (K, 62 ± 54 μM) and a second phase characterized by higher V (V, 61 ± 16 pmol s mg) and K (K, 1784 ± 833 μM). Data were confirmed in control experiments carried out in rat muscle samples with different percentages of MyHC isoforms. Correlation and receiver operating characteristics analyses suggest that the two phases of the response were related to the % of MyHC isoforms.
CONCLUSIONS
A novel mathematical approach (two sequential hyperbolic functions) for the fitting of JO versus [ADP] data obtained by high-resolution respirometry on permeabilized skeletal muscle fibres, obtained in humans and rats, provided an alternative fitting of the experimental data compared to the traditional Michaelis-Menten kinetics equation. This alternative model allowed the identification of two distinct phases in the responses, which were related to fibre type composition. A first phase, characterized by low apparent K and V values, was correlated with the percentage of less oxidative (Type 2A + 2X) MyHC isoforms. A second phase, characterized by high apparent K and V, was related to more oxidative (Type 1) MyHC isoforms.
MeSH
Myosin Heavy Chains, Muscles, Respiration, Protein Isoforms, Bed Rest, Beds, Muscle, Skeletal, Cachexia, Sarcopenia