Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Larsen 2014 Biochim Biophys Acta

From Bioblast
Revision as of 16:53, 10 February 2015 by Marte Verena (talk | contribs)
Publications in the MiPMap
Larsen S, Díez-Sánchez C, Rabøl R, Royo IA, Dela F, Helge JW (2013) Increased intrinsic mitochondrial function in humans with mitochondrial haplogroup H. Biochim Biophys Acta [Epub ahead of print]

» PMID: 24184346

Larsen S, Diez-Sanchez C, Raboel R, Royo IA, Dela F, Helge JW (2013) Biochim Biophys Acta

Abstract: It has been suggested that human mitochondrial variants influence maximal oxygen uptake (VO2max). Whether mitochondrial respiratory capacity per mitochondrion (intrinsic activity) in human skeletal muscle is affected by differences in mitochondrial variants is not known. We recruited 54 males and determined their mitochondrial haplogroup, mitochondrial oxidative phosphorylation capacity (OXPHOS), mitochondrial content (citrate synthase (CS)) and VO2max. Intrinsic mitochondrial function is calculated as mitochondrial OXPHOS capacity divided by mitochondrial content (CS). Haplogroup H showed a 30% higher intrinsic mitochondrial function compared with the other haplo group U. There was no relationship between haplogroups and VO2max. In skeletal muscle from men with mitochondrial haplogroup H, an increased intrinsic mitochondrial function is present. Keywords: Caucasian mitochondrial haplogroup, Intrinsic mitochondrial function, Mitochondrial OXPHOS capacity

O2k-Network Lab: DK Copenhagen Dela F


Labels: MiParea: Respiration, mtDNA;mt-genetics, Comparative MiP;environmental MiP 


Organism: Human  Tissue;cell: Skeletal muscle  Preparation: Permeabilized tissue  Enzyme: TCA cycle and matrix dehydrogenases 

Coupling state: LEAK, OXPHOS 

HRR: Oxygraph-2k 

[Epub ahead of print]