TY - JOUR
T1 - Biomarkers of mitochondrial content in skeletal muscle of healthy young human subjects
AU - Larsen, Steen
AU - Nielsen, Joachim
AU - Hansen, Christina Neigaard
AU - Nielsen, Lars Bo
AU - Wibrand, Flemming
AU - Stride, Nis Ottesen
AU - Schroder, Henrik Daa
AU - Boushel, Robert Christopher
AU - Helge, Jørn Wulff
AU - Dela, Flemming
AU - Hey-Mogensen, Martin
N1 - Published online before print May 14
PY - 2012
Y1 - 2012
N2 - Key points Several biochemical measures of mitochondrial components are used as biomarkers of mitochondrial content and muscle oxidative capacity. However, no studies have validated these surrogates against a morphological measure of mitochondrial content in human subjects. The most commonly used markers (citrate synthase activity, cardiolipin content, mitochondrial DNA content (mtDNA), complex I-V protein, and complex I-IV activity) were correlated with a measure of mitochondrial content (transmission electron microscopy) and muscle oxidative capacity (respiration in permeabilized fibres). Cardiolipin content followed by citrate synthase activity and complex I activity were the biomarkers showing the strongest association with mitochondrial content. mtDNA was found to be a poor biomarker of mitochondrial content. Complex IV activity was closely associated with mitochondrial oxidative phosphorylation capacity.
AB - Key points Several biochemical measures of mitochondrial components are used as biomarkers of mitochondrial content and muscle oxidative capacity. However, no studies have validated these surrogates against a morphological measure of mitochondrial content in human subjects. The most commonly used markers (citrate synthase activity, cardiolipin content, mitochondrial DNA content (mtDNA), complex I-V protein, and complex I-IV activity) were correlated with a measure of mitochondrial content (transmission electron microscopy) and muscle oxidative capacity (respiration in permeabilized fibres). Cardiolipin content followed by citrate synthase activity and complex I activity were the biomarkers showing the strongest association with mitochondrial content. mtDNA was found to be a poor biomarker of mitochondrial content. Complex IV activity was closely associated with mitochondrial oxidative phosphorylation capacity.
U2 - 10.1113/jphysiol.2012.230185
DO - 10.1113/jphysiol.2012.230185
M3 - Journal article
C2 - 22586215
SN - 0022-3751
VL - 590
SP - 3349
EP - 3360
JO - Journal of Physiology
JF - Journal of Physiology
IS - Pt 14
ER -