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Difference between revisions of "Heerlein 2005 Am J Respir Cell Mol Biol"

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{{Publication
{{Publication
|title=Heerlein K, Schulze A, Hotz L, Bartsch P, Mairbäurl H (2005) Hypoxia decreases cellular ATP demand and inhibits mitochondrial respiration of a549 cells. Am. J. Respir. Cell. Mol. Biol. 32: 44-51.
|title=Heerlein K, Schulze A, Hotz L, Bartsch P, Mairbäurl H (2005) Hypoxia decreases cellular ATP demand and inhibits mitochondrial respiration of a549 cells. Am. J. Respir. Cell. Mol. Biol. 32: 44-51.
|authors=Heerlein K, Schulze A, Hotz L, Bartsch P, Mairbaeurl H  
|authors=Heerlein K, Schulze A, Hotz L, Bartsch P, Mairbaeurl H
|year=2005
|year=2005
|journal=Am. J. Respir. Cell. Mol. Biol.
|journal=Am. J. Respir. Cell. Mol. Biol.
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|topics=Respiration; OXPHOS; ETS Capacity, ATP; ADP; AMP; PCr
|topics=Respiration; OXPHOS; ETS Capacity, ATP; ADP; AMP; PCr
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|articletype=Protocol; Manual
}}
}}

Revision as of 11:51, 20 October 2010

Publications in the MiPMap
Heerlein K, Schulze A, Hotz L, Bartsch P, Mairbäurl H (2005) Hypoxia decreases cellular ATP demand and inhibits mitochondrial respiration of a549 cells. Am. J. Respir. Cell. Mol. Biol. 32: 44-51.

» PMID: 15388515

Heerlein K, Schulze A, Hotz L, Bartsch P, Mairbaeurl H (2005) Am. J. Respir. Cell. Mol. Biol.

Abstract: 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-ATPase–related JO2 was decreased by ~ 25% in hypoxia. Inhibition of other ion transporters did not affect JO2. Protein synthesis–related 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 30–40%. 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. Keywords: Energy metabolism, Hypoxia, Mitochondrial electron transfer chain, Na-transport, respirometry

O2k-Network Lab: DE_Heidelberg_MaierbaeuerlH


Labels:

Stress:Hypoxia, Mitochondrial Disease; Degenerative Disease and Defect"Mitochondrial Disease; Degenerative Disease and Defect" is not in the list (Cell death, Cryopreservation, Ischemia-reperfusion, Permeability transition, Oxidative stress;RONS, Temperature, Hypoxia, Mitochondrial disease) of allowed values for the "Stress" property.  Organism: Rat  Tissue;cell: Blood Cell; Suspension Culture"Blood Cell; Suspension Culture" is not in the list (Heart, Skeletal muscle, Nervous system, Liver, Kidney, Lung;gill, Islet cell;pancreas;thymus, Endothelial;epithelial;mesothelial cell, Blood cells, Fat, ...) of allowed values for the "Tissue and cell" property. 


Regulation: Respiration; OXPHOS; ETS Capacity"Respiration; OXPHOS; ETS Capacity" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property., ATP; ADP; AMP; PCr"ATP; ADP; AMP; PCr" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property. 


HRR: Oxygraph-2k