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Difference between revisions of "Schneider 2007 Cell Biol Int"

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{{Publication
{{Publication
|title=Schneider N, Mouithys-Mickalad A, Lejeune JP, Duyckaerts C, Sluse F, Deby-Dupont G, Serteyn D (2007) Oxygen consumption of equine articular chondrocytes: Influence of applied oxygen tension and glucose concentration during culture. Cell. Biol. Int. 31: 878-886.
|title=Schneider N, Mouithys-Mickalad A, Lejeune JP, Duyckaerts C, Sluse F, Deby-Dupont G, Serteyn D (2007) Oxygen consumption of equine articular chondrocytes: Influence of applied oxygen tension and glucose concentration during culture. Cell Biol Int 31:878-86.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/17442596 PMID: 17442596]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/17442596 PMID: 17442596]
|authors=Schneider N, Mouithys Mickalad A, Lejeune JP, Duyckaerts C, Sluse F, Deby-Dupont G, Serteyn D
|authors=Schneider N, Mouithys-Mickalad A, Lejeune JP, Duyckaerts C, Sluse F, Deby-Dupont G, Serteyn D
|year=2007
|year=2007
|journal=Cell. Biol. Int.
|journal=Cell Biol Int
|abstract=We investigated the oxygen (O<sub>2</sub>) uptake of equine articular chondrocytes to assess their reactions to anoxia/re-oxygenation. They were cultured under 5% or 21% gas phase O<sub>2</sub> and at glucose concentrations of 0, 1.0 or 4.5g/L in the culture medium (n=3). Afterwards, the O<sub>2</sub> consumption rate of the chondrocytes was monitored (oxymetry) before and after an anoxia period of 25min. The glucose consumption and lactate release were measured at the end of the re-oxygenation period. The chondrocytes showed a minimal O<sub>2</sub> consumption rate, which was hardly changed by anoxia. Independently from the O<sub>2</sub> tension, glucose uptake by the cells was about 30% of the available culture medium glucose, thus higher for cells at 4.5g/L glucose (n=3). Lactate release was also independent from O<sub>2</sub> tension, but lower for cells at 4.5g/L glucose (n=3). Our observations indicated that O<sub>2</sub> consumption by equine chondrocytes was very low despite a functional mitochondrial respiratory chain, and nearly insensitive to anoxia/re-oxygenation. But the chondrocytes metabolism was modified by an excess of O<sub>2</sub> and glucose.
|abstract=We investigated the oxygen (O<sub>2</sub>) uptake of equine articular chondrocytes to assess their reactions to anoxia/re-oxygenation. They were cultured under 5% or 21% gas phase O<sub>2</sub> and at glucose concentrations of 0, 1.0 or 4.5g/L in the culture medium (n=3). Afterwards, the O<sub>2</sub> consumption rate of the chondrocytes was monitored (oxymetry) before and after an anoxia period of 25min. The glucose consumption and lactate release were measured at the end of the re-oxygenation period. The chondrocytes showed a minimal O<sub>2</sub> consumption rate, which was hardly changed by anoxia. Independently from the O<sub>2</sub> tension, glucose uptake by the cells was about 30% of the available culture medium glucose, thus higher for cells at 4.5g/L glucose (n=3). Lactate release was also independent from O<sub>2</sub> tension, but lower for cells at 4.5g/L glucose (n=3). Our observations indicated that O<sub>2</sub> consumption by equine chondrocytes was very low despite a functional mitochondrial respiratory chain, and nearly insensitive to anoxia/re-oxygenation. But the chondrocytes metabolism was modified by an excess of O<sub>2</sub> and glucose.
|keywords=Chondrocytes, Anoxia, Lactate, Glucose
|keywords=Chondrocytes, Anoxia, Lactate, Glucose
|mipnetlab=BE_Liege_Votion DM
|mipnetlab=BE Liege Votion DM
|discipline=Mitochondrial Physiology
|discipline=Mitochondrial Physiology
}}
}}
{{Labeling
{{Labeling
|area=Respiration
|injuries=Hypoxia
|organism=Horse
|topics=Substrate
|couplingstates=OXPHOS
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|injuries=Hypoxia, RONS; Oxidative Stress
|organism=Other Mammal
|kinetics=Oxygen
|topics=Respiration; OXPHOS; ETS Capacity, Substrate; Glucose; TCA Cycle
|discipline=Mitochondrial Physiology
|discipline=Mitochondrial Physiology
}}
}}

Latest revision as of 16:33, 4 June 2017

Publications in the MiPMap
Schneider N, Mouithys-Mickalad A, Lejeune JP, Duyckaerts C, Sluse F, Deby-Dupont G, Serteyn D (2007) Oxygen consumption of equine articular chondrocytes: Influence of applied oxygen tension and glucose concentration during culture. Cell Biol Int 31:878-86.

Β» PMID: 17442596

Schneider N, Mouithys-Mickalad A, Lejeune JP, Duyckaerts C, Sluse F, Deby-Dupont G, Serteyn D (2007) Cell Biol Int

Abstract: We investigated the oxygen (O2) uptake of equine articular chondrocytes to assess their reactions to anoxia/re-oxygenation. They were cultured under 5% or 21% gas phase O2 and at glucose concentrations of 0, 1.0 or 4.5g/L in the culture medium (n=3). Afterwards, the O2 consumption rate of the chondrocytes was monitored (oxymetry) before and after an anoxia period of 25min. The glucose consumption and lactate release were measured at the end of the re-oxygenation period. The chondrocytes showed a minimal O2 consumption rate, which was hardly changed by anoxia. Independently from the O2 tension, glucose uptake by the cells was about 30% of the available culture medium glucose, thus higher for cells at 4.5g/L glucose (n=3). Lactate release was also independent from O2 tension, but lower for cells at 4.5g/L glucose (n=3). Our observations indicated that O2 consumption by equine chondrocytes was very low despite a functional mitochondrial respiratory chain, and nearly insensitive to anoxia/re-oxygenation. But the chondrocytes metabolism was modified by an excess of O2 and glucose. β€’ Keywords: Chondrocytes, Anoxia, Lactate, Glucose

β€’ O2k-Network Lab: BE Liege Votion DM


Labels: MiParea: Respiration 

Stress:Hypoxia  Organism: Horse 


Regulation: Substrate  Coupling state: OXPHOS 

HRR: Oxygraph-2k