Huetter 2002 Mol Biol Rep: Difference between revisions

From Bioblast
No edit summary
Β 
(18 intermediate revisions by 7 users not shown)
Line 1: Line 1:
{{Publication
{{Publication
|title=HΓΌtter E, Renner K, Jansen-DΓΌrr P, Gnaiger E (2002) Biphasic oxygen kinetics of cellular respiration and linear oxygen dependence of antimycin A inhibited oxygen consumption. Mol Biol Rep 29: 83-87.
|title=HΓΌtter E, Renner K, Jansen-DΓΌrr P, Gnaiger E (2002) Biphasic oxygen kinetics of cellular respiration and linear oxygen dependence of antimycin A inhibited oxygen consumption. Mol Biol Rep 29:83-7.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/12241081 PMID: 12241081]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/12241081 PMID: 12241081]
|authors=Huetter E, Renner K, Jansen-Duerr P, Gnaiger E
|authors=Huetter E, Renner K, Jansen-Duerr P, Gnaiger Erich
|year=2002
|year=2002
|journal=Mol Biol Rep
|journal=Mol Biol Rep
|abstract=Oxygen kinetics in fibroblasts was biphasic. This was quantitatively explained by a major mitochondrial hyperbolic component in the low-oxygen range and a linear increase of rotenone- and antimycin A- inhibited oxygen consumption in the high-oxygen range. This suggest an increased production of reactive oxygen species and oxidative stress at elevated, air-level oxygen concentrations. The high oxygen activity of mitochondrial respiration provides the basis for the maintenance of a high aerobic scope at physiological low-oxygen levels, whereas further pronounced depression induces energetic stress under hypoxia.
|abstract=Oxygen kinetics in fibroblasts was biphasic. This was quantitatively explained by a major mitochondrial hyperbolic component in the low-oxygen range and a linear increase of rotenone- and antimycin A- inhibited oxygen consumption in the high-oxygen range. This suggest an increased production of reactive oxygen species and oxidative stress at elevated, air-level oxygen concentrations. The high oxygen activity of mitochondrial respiration provides the basis for the maintenance of a high aerobic scope at physiological low-oxygen levels, whereas further pronounced depression induces energetic stress under hypoxia.
|mipnetlab=AT_Innsbruck_Gnaiger E, AT_Innsbruck_Jansen-Duerr P, AT Innsbruck MitoCom
|mipnetlab=AT Innsbruck Gnaiger E, AT Innsbruck Jansen-Duerr P, AT Innsbruck Oroboros , DE Regensburg Renner-Sattler K
|discipline=Mitochondrial Physiology
}}
}}
== Cited by ==
::* 8 articles in PubMed (2024-01-11) https://pubmed.ncbi.nlm.nih.gov/12241081/
{{Template:Cited by Komlodi 2021 MitoFit AmR}}
{{Labeling
{{Labeling
|area=Respiration
|organism=Human
|tissues=Fibroblast
|preparations=Intact cells
|topics=Oxygen kinetics
|couplingstates=ROUTINE
|pathways=ROX
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|injuries=Hypoxia
|additional=MitoFit 2021 AmR
|organism=Human
|model cell lines=Fibroblast
|preparations=Intact Cell; Cultured; Primary
|couplingstates=OXPHOS
|kinetics=Oxygen
|discipline=Mitochondrial Physiology
}}
}}

Latest revision as of 08:12, 11 January 2024

Publications in the MiPMap
HΓΌtter E, Renner K, Jansen-DΓΌrr P, Gnaiger E (2002) Biphasic oxygen kinetics of cellular respiration and linear oxygen dependence of antimycin A inhibited oxygen consumption. Mol Biol Rep 29:83-7.

Β» PMID: 12241081

Huetter E, Renner K, Jansen-Duerr P, Gnaiger Erich (2002) Mol Biol Rep

Abstract: Oxygen kinetics in fibroblasts was biphasic. This was quantitatively explained by a major mitochondrial hyperbolic component in the low-oxygen range and a linear increase of rotenone- and antimycin A- inhibited oxygen consumption in the high-oxygen range. This suggest an increased production of reactive oxygen species and oxidative stress at elevated, air-level oxygen concentrations. The high oxygen activity of mitochondrial respiration provides the basis for the maintenance of a high aerobic scope at physiological low-oxygen levels, whereas further pronounced depression induces energetic stress under hypoxia.


β€’ O2k-Network Lab: AT Innsbruck Gnaiger E, AT Innsbruck Jansen-Duerr P, AT Innsbruck Oroboros, DE Regensburg Renner-Sattler K

Cited by

  • KomlΓ³di T, Schmitt S, Zdrazilova L, Donnelly C, Zischka H, Gnaiger E. Oxygen dependence of hydrogen peroxide production in isolated mitochondria and permeabilized cells. MitoFit Preprints (in prep).

Labels: MiParea: Respiration 


Organism: Human  Tissue;cell: Fibroblast  Preparation: Intact cells 

Regulation: Oxygen kinetics  Coupling state: ROUTINE  Pathway: ROX  HRR: Oxygraph-2k 

MitoFit 2021 AmR 

Cookies help us deliver our services. By using our services, you agree to our use of cookies.