Hyperoxia decreases glycolytic capacity, glycolytic reserve and oxidative phosphorylation in MLE-12 cells and inhibits complex I and II function, but not complex IV in isolated mouse lung mitochondria.

PloS one

Volumn 8, Issue 9, 2013, Pages

  Das, Kumuda C ^a  

^a TEXAS TECH UNIVERSITY HEALTH SCIENCES CENTER SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; OXYGEN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); SUCCINATE DEHYDROGENASE (UBIQUINONE);

ANIMAL; CELL LINE; CYTOLOGY; ELECTRON TRANSPORT; ENERGY METABOLISM; EXTRACELLULAR SPACE; FEMALE; GLYCOLYSIS; LUNG; MALE; METABOLISM; MITOCHONDRION; MOUSE; OXIDATIVE PHOSPHORYLATION;

ANIMALS; CELL LINE; ELECTRON TRANSPORT; ELECTRON TRANSPORT COMPLEX I; ELECTRON TRANSPORT COMPLEX II; ELECTRON TRANSPORT COMPLEX IV; ENERGY METABOLISM; EXTRACELLULAR SPACE; FEMALE; GLYCOLYSIS; LUNG; MALE; MICE; MITOCHONDRIA; OXIDATIVE PHOSPHORYLATION; OXYGEN;

EID: 84890357795     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0073358     Document Type: Article

References (0)