Difference between revisions of "Neufer 2014 Abstract MiP2014"
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{{Abstract | {{Abstract | ||
|title=Assessing ATP production and oxygen consumption simultaneously in permeabilized fibers: ATP/O. | |title=Assessing ATP production and oxygen consumption simultaneously in permeabilized fibers: ATP/O. | ||
|info=[[File: | |info=[[File:Neufer_PD.jpg|150px|right|Neufer DP]] [[Laner 2014 Mitochondr Physiol Network MiP2014|Mitochondr Physiol Network 19.13]] - [http://www.mitophysiology.org/index.php?mip2014 MiP2014] | ||
|authors=Lark DS, Ryan | |authors=Lark DS, Ryan TE, Anderson EJ, Neufer PD | ||
|year=2014 | |year=2014 | ||
|event=MiP2014 | |event=MiP2014 | ||
|abstract=The biochemical efficiency of oxidative phosphorylation (OXPHOS), quantified as the amount of ATP produced per oxygen atom consumed (ATP/O or ~P/O), is vital to maintaining proper myocyte energetics. However, despite its central importance, it is difficult to experimentally determine the ~P/O ratio as a function of metabolic demand, and therefore, the relationship between OXPHOS efficiency and metabolic demand is poorly understood. O<sub>2</sub> consumption (high-resolution respirometry) and ATP production (determined fluorometrically using a 2-deoxyglucose – hexokinase – glucose-6-phosphate dehydrogenase – NADP<sup>+</sup> respiratory clamp system [1]), rates were measured simultaneously in permeabilized mouse oxidative and glycolytic skeletal muscle fiber bundles using a customized Oroboros Oxygraph-2k. | |||
With pyruvate+malate (5+2 mM) as substrate, at low [ADP] (5-20 µM), the ~P/O ratio increased as a function of [ADP], independent of an increase in O<sub>2</sub> consumption. Maximal ~P/O peaked at ~2.0 and was not different between oxidative and glycolytic muscle. Pharmacological inhibition of adenylate kinase decreased ATP production rate but did not alter ADP-dependent increases in OXPHOS efficiency. | |||
These findings suggest that mitochondria respond to low levels of metabolic demand by initially increasing OXPHOS efficiency. | |||
|mipnetlab=US NC Greenville Neufer PD, US NC Greenville Anderson EJ | |||
}} | }} | ||
{{Labeling | {{Labeling | ||
| Line 11: | Line 18: | ||
|tissues=Skeletal muscle | |tissues=Skeletal muscle | ||
|preparations=Permeabilized tissue | |preparations=Permeabilized tissue | ||
|topics=ADP, ATP production | |topics=ADP, ATP production, Coupling efficiency;uncoupling | ||
|couplingstates=OXPHOS | |couplingstates=OXPHOS | ||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
|event=A4, Oral | |||
|additional=MiP2014 | |additional=MiP2014 | ||
}} | }} | ||
== Affiliation == | == Affiliation == | ||
1-East Carolina Diabetes Obesity Inst; 2-Dep Kinesiolog; 3-Dep Physiol; 4-Dep Pharmacolog Toxicolog; East Carolina Univ, Greenville, NC, USA. – [email protected] | 1-East Carolina Diabetes Obesity Inst; 2-Dep Kinesiolog; 3-Dep Physiol; 4-Dep Pharmacolog Toxicolog; East Carolina Univ, Greenville, NC, USA. – [email protected] | ||
== References and acknowledgements == | |||
Supported by: National Institute of Health R01 DK096907 (USA). | |||
# Gouspillou G, Rouland R, Calmettes G, Deschodt-Arsac V, Franconi J-M, Bourdel-Marchasson I, Diolez P (2011) Accurate determination of the oxidative phosphorylation affinity for ADP in isolated mitochondria. PloS One 6:e20709. | |||
Latest revision as of 13:04, 23 January 2019
| Assessing ATP production and oxygen consumption simultaneously in permeabilized fibers: ATP/O. |
Link:
Mitochondr Physiol Network 19.13 - MiP2014
Lark DS, Ryan TE, Anderson EJ, Neufer PD (2014)
Event: MiP2014
The biochemical efficiency of oxidative phosphorylation (OXPHOS), quantified as the amount of ATP produced per oxygen atom consumed (ATP/O or ~P/O), is vital to maintaining proper myocyte energetics. However, despite its central importance, it is difficult to experimentally determine the ~P/O ratio as a function of metabolic demand, and therefore, the relationship between OXPHOS efficiency and metabolic demand is poorly understood. O2 consumption (high-resolution respirometry) and ATP production (determined fluorometrically using a 2-deoxyglucose – hexokinase – glucose-6-phosphate dehydrogenase – NADP+ respiratory clamp system [1]), rates were measured simultaneously in permeabilized mouse oxidative and glycolytic skeletal muscle fiber bundles using a customized Oroboros Oxygraph-2k.
With pyruvate+malate (5+2 mM) as substrate, at low [ADP] (5-20 µM), the ~P/O ratio increased as a function of [ADP], independent of an increase in O2 consumption. Maximal ~P/O peaked at ~2.0 and was not different between oxidative and glycolytic muscle. Pharmacological inhibition of adenylate kinase decreased ATP production rate but did not alter ADP-dependent increases in OXPHOS efficiency.
These findings suggest that mitochondria respond to low levels of metabolic demand by initially increasing OXPHOS efficiency.
• O2k-Network Lab: US NC Greenville Neufer PD, US NC Greenville Anderson EJ
Labels: MiParea: Respiration
Organism: Mouse
Tissue;cell: Skeletal muscle
Preparation: Permeabilized tissue
Regulation: ADP, ATP production, Coupling efficiency;uncoupling Coupling state: OXPHOS
HRR: Oxygraph-2k Event: A4, Oral MiP2014
Affiliation
1-East Carolina Diabetes Obesity Inst; 2-Dep Kinesiolog; 3-Dep Physiol; 4-Dep Pharmacolog Toxicolog; East Carolina Univ, Greenville, NC, USA. – [email protected]
References and acknowledgements
Supported by: National Institute of Health R01 DK096907 (USA).
- Gouspillou G, Rouland R, Calmettes G, Deschodt-Arsac V, Franconi J-M, Bourdel-Marchasson I, Diolez P (2011) Accurate determination of the oxidative phosphorylation affinity for ADP in isolated mitochondria. PloS One 6:e20709.
