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Difference between revisions of "Krivakova 2007 Physiol Res"

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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.
|authors=Krivakova P, Labajova A, Cervinkova Z, Drahota Z
|info=[http://www.ncbi.nlm.nih.gov/pubmed/17381246 PMID: 17381246 Open Access]
|authors=Stankova Pavla, Labajova Anna, Cervinkova Zuzana, Drahota Zdenek
|year=2007
|year=2007
|journal=Physiological Research
|journal=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
|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
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
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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
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.
represents a useful tool for evaluation of changes participating in peroxidative damage of cell energy metabolism.
|keywords=Hepatocytes, Oxidative phosphorylation, t-Butyl hydroperoxide Β 
|keywords=Hepatocytes, Oxidative phosphorylation, t-Butyl hydroperoxide
|info=[http://www.ncbi.nlm.nih.gov/pubmed/17381246 PMID: 17381246]
|mipnetlab=CZ Hradec Kralove Cervinkova Z
|discipline=Mitochondrial Physiology
}}
}}
{{Labeling
{{Labeling
|discipline=Mitochondrial Physiology
|organism=Rat
|organism=Rat
|enzymes=Complex I, Complex II; Succinate Dehydrogenase, Uncoupler Protein
|tissues=Liver
|kinetics=ADP; Pi, Oxygen, Reduced Substrate; Cytochrome c
|preparations=Isolated mitochondria
|topics=Respiration; OXPHOS; ETS Capacity, Coupling; Membrane Potential, Ion Homeostasis
|injuries=Oxidative stress;RONS
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|articletype=Protocol; Manual
|discipline=Mitochondrial Physiology
}}
}}

Latest revision as of 10:13, 18 March 2020

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 Open Access

Stankova Pavla, Labajova Anna, Cervinkova Zuzana, Drahota Zdenek (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