Mitochondrial Function in an In Vitro Model of Skeletal Muscle of Patients With Protracted Critical Illness and Intensive Care Unit-Acquired Weakness
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
27358332
DOI
10.1177/0148607116657649
PII: 0148607116657649
Knihovny.cz E-zdroje
- Klíčová slova
- ICU-acquired weakness, extracellular flux analysis, fatty acid oxidation, human skeletal muscle, mitochondrial function, protracted critical illness,
- MeSH
- čtyřhlavý sval stehenní MeSH
- energetický metabolismus * MeSH
- fyziologická adaptace MeSH
- inzulin krev MeSH
- inzulinová rezistence MeSH
- jednotky intenzivní péče * MeSH
- kosterní svalová vlákna MeSH
- kosterní svaly cytologie patofyziologie MeSH
- krevní glukóza metabolismus MeSH
- kritický stav * MeSH
- kyseliny mastné neesterifikované metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- lipolýza MeSH
- respirační komplex II metabolismus MeSH
- senioři MeSH
- svalová slabost etiologie metabolismus patofyziologie MeSH
- svalové mitochondrie fyziologie MeSH
- transport elektronů MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- inzulin MeSH
- krevní glukóza MeSH
- kyseliny mastné neesterifikované MeSH
- respirační komplex II MeSH
- respiratory complex II MeSH Prohlížeč
BACKGROUND: Functional mitochondria in skeletal muscle of patients with protracted critical illness and intensive care unit-acquired weakness are depleted, but remaining mitochondria have increased functional capacities of respiratory complexes II and III. This can be an adaptation to relative abundancy of fatty acid over glucose caused by insulin resistance. We hypothesized that the capacity of muscle mitochondria to oxidize fatty acid is increased in protracted critical illness. METHODS: We assessed fatty acid oxidation (FAO) and mitochondrial functional indices in vitro by using extracellular flux analysis in cultured myotubes obtained by isolating and culturing satellite cells from vastus lateralis muscle biopsy samples from patients with ICU-acquired weakness (n = 6) and age-matched healthy controls (n = 7). Bioenergetic measurements were performed at baseline and after 6 days of exposure to free fatty acids (FFAs). RESULTS: Mitochondrial density in myotubes from ICU patients was 69% of healthy controls ( P = .051). After adjustment to mitochondrial content, there were no differences in adenosine triphosphate (ATP) synthesis or the capacity and coupling of the respiratory chain. FAO capacity in ICU patients was 157% of FAO capacity in controls ( P = .015). In myotubes of ICU patients, unlike healthy controls, the exposure to FFA significantly ( P = .009) increased maximum respiratory chain capacity. CONCLUSION: In an in vitro model of skeletal muscle of patients with protracted critical illness, we have shown signs of adaptation to increased FAO. Even in the presence of glucose and insulin, elevation of FFAs in the extracellular environment increased maximal capacity of the respiratory chain.
Department of Cell Biology Faculty of Science Charles University Prague Prague Czech Republic
Department of Internal Medicine 2 Kralovske Vinohrady University Hospital Prague Czech Republic
Department of Orthopaedic Surgeries Kralovske Vinohrady University Hospital Prague Czech Republic
Laboratory of Bioenergetics 3rd Faculty of Medicine Charles University Prague Prague Czech Republic
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