Published ahead of print on September 23, 2004, doi:10.1165/rcmb.2004-0202OC
American Journal of Respiratory Cell and Molecular Biology. Vol. 32, pp. 44-51, 2005
© 2005 American Thoracic Society DOI: 10.1165/rcmb.2004-0202OC
Hypoxia Decreases Cellular ATP Demand and Inhibits Mitochondrial Respiration of A549 Cells
Kristin Heerlein,
Andreas Schulze,
Lorenz Hotz,
Peter Bärtsch and
Heimo Mairbäurl
Medical Clinic VII, Sports Medicine, University of Heidelberg; and Division of Metabolic and Endocrine Diseases, Department of General Pediatrics, University Children's Hospital, Heidelberg, Germany
Correspondence and requests for reprints should be addressed to Heimo Mairbäurl, Medical Clinic VII, Sports Medicine, University of Heidelberg, INF 410, 69120 Heidelberg, Germany. E-mail: heimo.mairbaeurl{at}med.uni-heidelberg.de
Hypoxia inhibits activity and expression of transporters involved in alveolar Na reabsorption and fluid clearance. We studied whether this represents a mechanism for reducing energy consumption or whether it is the consequence of metabolic dysfunction. Oxygen consumption (JO2) of A549 cells and primary rat alveolar type II cells was measured by microrespirometry during normoxia, hypoxia (1.5% O2), and reoxygenation. In both cell types, acute and 24-h hypoxia decreased total JO2 significantly and reoxygenation restored JO2 after 5 min but not after 24 h of hypoxia in A549 cells, whereas recovery was complete in type II cells. In A549 cells under normoxia Na/K-ATPase accounted for 15% of JO2, whereas Na/K-ATPaserelated JO2 was decreased by 25% in hypoxia. Inhibition of other ion transporters did not affect JO2. Protein synthesisrelated JO2 was not affected by acute hypoxia, but decreased by 30% after 24-h hypoxia. Acute and 24-h hypoxia decreased JO2 of A549 cell mitochondrial complexes I, II, and III by 3040%. Reoxygenation restored complex I activity after acute hypoxia but not after 24-h hypoxia. ATP was decreased 30% after 24-h hypoxia, but lactate production rate was not affected. Reduced nicotinamine adenine dinucleotide was slightly elevated in acute hypoxia. Our findings indicate that inhibition of the Na/K-ATPase by hypoxia contributes little to energy preservation in hypoxia. It remains unclear to what extent hypoxic inhibition of mitochondrial metabolism affects ATP-consuming processes.
Key Words: energy metabolism hypoxia mitochondrial electron transfer chain Na-transport respirometry
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