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Difference between revisions of "Krivakova 2007 Physiol Res"

From Bioblast
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{{Publication
{{Publication
|title=Krivakova P, Labajova A, Cervinkova Z, Drahota Z (2007) Inhibitory effect of t-butyl hydroperoxide on mitochondrial oxidative phosphorylation in isolated rat hepatocytes. Physiol Res 56: 137-140.
|title=Krivakova P, Labajova A, Cervinkova Z, Drahota Z (2007) Inhibitory effect of t-butyl hydroperoxide on mitochondrial oxidative phosphorylation in isolated rat hepatocytes. Physiol Res 56:137-40.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/17381246 PMID: 17381246]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/17381246 PMID: 17381246]
|authors=Krivakova P, Labajova A, Cervinkova Z, Drahota Z
|authors=Krivakova P, Labajova A, Cervinkova Z, Drahota Z
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}}
}}
{{Labeling
{{Labeling
|instruments=Oxygraph-2k
|injuries=RONS; Oxidative Stress
|organism=Rat
|organism=Rat
|tissues=Liver
|tissues=Liver
|preparations=Isolated Mitochondria
|preparations=Isolated mitochondria
|injuries=Oxidative stress;RONS
|instruments=Oxygraph-2k
|discipline=Mitochondrial Physiology
|discipline=Mitochondrial Physiology
}}
}}

Revision as of 13:30, 13 February 2015

Publications in the MiPMap
Krivakova P, Labajova A, Cervinkova Z, Drahota Z (2007) Inhibitory effect of t-butyl hydroperoxide on mitochondrial oxidative phosphorylation in isolated rat hepatocytes. Physiol Res 56:137-40.

Β» PMID: 17381246

Krivakova P, Labajova A, Cervinkova Z, Drahota Z (2007) Physiol Res

Abstract: Using high-resolution oxygraphy, we tested the changes of various parameters characterizing the mitochondrial energy provision system that were induced by peroxidative damage. In the presence of succinate as respiratory substrate, 3 mM t-butyl hydroperoxide increased respiration in the absence of ADP, which indicated partial uncoupling of oxidative phosphorylation. Low activity of coupled respiration was still maintained as indicated by the ADP-activated and oligomycin-inhibited respiration. However, during the incubation the phosphorylative capacity decreased as indicated by the continuous decrease of the mitochondrial membrane potential. Under these experimental conditions the maximum capacity of the succinate oxidase system was inhibited by 50 % in comparison with values obtained in the absence of t-butyl hydroperoxide. Our data thus indicate that the oxygraphic evaluation of mitochondrial function represents a useful tool for evaluation of changes participating in peroxidative damage of cell energy metabolism. β€’ Keywords: Hepatocytes, Oxidative phosphorylation, t-Butyl hydroperoxide

β€’ O2k-Network Lab: CZ_Hradec Kralove_Cervinkova Z


Labels:

Stress:Oxidative stress;RONS  Organism: Rat  Tissue;cell: Liver  Preparation: Isolated mitochondria 



HRR: Oxygraph-2k