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Difference between revisions of "Gnaiger 2011 Abstract-MonteVerita"

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|year=2011
|year=2011
|event=Monte Verita
|event=Monte Verita
|abstract='''Mitochondrial capacity''': [[OXPHOS]] capacity is evaluated in isolated mitochondria (mt) and permeabilized cells with physiological substrate cocktails to reconstitute tricarboxylic acid cycle function. As a consequence, convergent electron flow from Complexes CI+II of the electron transfer system ([[ETS]]) to the [[Q-junction]] exerts an additive effect on flux [1].
|abstract='''Mitochondrial capacity''': [[OXPHOS]] capacity is evaluated in isolated mitochondria (mt) and permeabilized cells with physiological substrate cocktails to reconstitute tricarboxylic acid cycle function. As a consequence, convergent electron flow from Complexes CI+II of the electron transfer-pathway ([[ET-pathway]]) to the [[Q-junction]] exerts an additive effect on flux [1].


'''Oxygen kinetics of mt-respiration''': The apparent ''K''<sub>m,O2</sub> or ''c''<sub>50</sub> [µM] (''p''<sub>50</sub> [kPa]) of mt-respiration increases linearly with respiratory capacity controlled by metabolic state, from 0.2 to 1.6 µM determined by [[high-resolution respirometry]]. O<sub>2</sub> gradients are significant only in large cells including cardiomyocytes. The apparent ''p''<sub>50</sub> increases 100-fold in permeabilized muscle fibers due to diffusion gradients [2].
'''Oxygen kinetics of mt-respiration''': The apparent ''K''<sub>m,O2</sub> or ''c''<sub>50</sub> [µM] (''p''<sub>50</sub> [kPa]) of mt-respiration increases linearly with respiratory capacity controlled by metabolic state, from 0.2 to 1.6 µM determined by [[high-resolution respirometry]]. O<sub>2</sub> gradients are significant only in large cells including cardiomyocytes. The apparent ''p''<sub>50</sub> increases 100-fold in permeabilized muscle fibers due to diffusion gradients [2].
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'''mt-function at ''V''<sub>O2max</sub>''': Aerobic capacity of the human leg muscle exceeds maximum O<sub>2</sub> uptake of isolated mitochondria [3] and v. lateralis during ''V''<sub>O2max</sub> [4]. Therefore, oxygen supply limits aerobic performance, proportional to the apparent mt-excess capacity [5]. mt-respiration is more sensitive to average ''p''<sub>O2</sub> in heterogenous tissues than under homogenous conditions in vitro. Tissue heterogeneity increases the kinetic dependence of flux on average intracellular ''p''<sub>O2</sub>. High mt-density reinforces the steepness of oxygen gradients and oxygen heterogeneity in the tissue, contributing to the O<sub>2</sub> limitation in athletic vs sedentary individuals at ''V''<sub>O2max</sub> [6]. This provides a functional rationale for the observation that hypoxia does not specifically trigger mt-biogenesis [7].
'''mt-function at ''V''<sub>O2max</sub>''': Aerobic capacity of the human leg muscle exceeds maximum O<sub>2</sub> uptake of isolated mitochondria [3] and v. lateralis during ''V''<sub>O2max</sub> [4]. Therefore, oxygen supply limits aerobic performance, proportional to the apparent mt-excess capacity [5]. mt-respiration is more sensitive to average ''p''<sub>O2</sub> in heterogenous tissues than under homogenous conditions in vitro. Tissue heterogeneity increases the kinetic dependence of flux on average intracellular ''p''<sub>O2</sub>. High mt-density reinforces the steepness of oxygen gradients and oxygen heterogeneity in the tissue, contributing to the O<sub>2</sub> limitation in athletic vs sedentary individuals at ''V''<sub>O2max</sub> [6]. This provides a functional rationale for the observation that hypoxia does not specifically trigger mt-biogenesis [7].


[[MitoCom#Acknowledgment|Contribution to K-Regio]] ''[[MitoCom_K-Regio|MitoCom Tyrol]]''.
Contribution to K-Regio ''[[MitoCom_O2k-Fluorometer|MitoCom Tyrol]]''.


[1] [[Gnaiger 2009 Int J Biochem Cell Biol|Gnaiger 2009]]; [[Lemieux_2011_Int J Biochem Cell Biol|Lemieux et al 2011 Int J Biochem Cell Biol]]  
[1] [[Gnaiger 2009 Int J Biochem Cell Biol|Gnaiger 2009]]; [[Lemieux_2011_Int J Biochem Cell Biol|Lemieux et al 2011 Int J Biochem Cell Biol]]  
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|area=Respiration
|area=Respiration
|organism=Human
|organism=Human
|injuries=Hypoxia
|topics=Oxygen kinetics, Substrate
|topics=O2, Substrate
|couplingstates=OXPHOS
|couplingstates=OXPHOS
|substratestates=CI, CII, CI&II
|pathways=N, S, NS
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|journal=Abstract
|journal=Abstract
}}
}}

Revision as of 10:15, 8 June 2020

Gnaiger E (2011) Mitochondrial respiratory capacity at maximum aerobic exercise levels: Are intracellular oxygen levels limiting? Abstract Monte Verita.

Link: The impact of hypoxia on cells, mice and men

Gnaiger E (2011)

Event: Monte Verita

Mitochondrial capacity: OXPHOS capacity is evaluated in isolated mitochondria (mt) and permeabilized cells with physiological substrate cocktails to reconstitute tricarboxylic acid cycle function. As a consequence, convergent electron flow from Complexes CI+II of the electron transfer-pathway (ET-pathway) to the Q-junction exerts an additive effect on flux [1].

Oxygen kinetics of mt-respiration: The apparent Km,O2 or c50 [µM] (p50 [kPa]) of mt-respiration increases linearly with respiratory capacity controlled by metabolic state, from 0.2 to 1.6 µM determined by high-resolution respirometry. O2 gradients are significant only in large cells including cardiomyocytes. The apparent p50 increases 100-fold in permeabilized muscle fibers due to diffusion gradients [2].

mt-function at VO2max: Aerobic capacity of the human leg muscle exceeds maximum O2 uptake of isolated mitochondria [3] and v. lateralis during VO2max [4]. Therefore, oxygen supply limits aerobic performance, proportional to the apparent mt-excess capacity [5]. mt-respiration is more sensitive to average pO2 in heterogenous tissues than under homogenous conditions in vitro. Tissue heterogeneity increases the kinetic dependence of flux on average intracellular pO2. High mt-density reinforces the steepness of oxygen gradients and oxygen heterogeneity in the tissue, contributing to the O2 limitation in athletic vs sedentary individuals at VO2max [6]. This provides a functional rationale for the observation that hypoxia does not specifically trigger mt-biogenesis [7].

Contribution to K-Regio MitoCom Tyrol.

[1] Gnaiger 2009; Lemieux et al 2011 Int J Biochem Cell Biol

[2] Gnaiger 2003; Scandurra, Gnaiger 2010 Adv Exp Med Biol.

[3] Rasmussen et al 2001 AJP.

[4] Boushel et al 2011 Mitochondrion.

[5] Gnaiger et al 1998 JEB.

[6] Richardson et al; Haseler et al JAP.

[7] Pesta et al 2011 AJP; Jacobs et al 2011 JAP.


O2k-Network Lab: AT Innsbruck Gnaiger E


Labels: MiParea: Respiration 


Organism: Human 


Regulation: Oxygen kinetics, Substrate  Coupling state: OXPHOS  Pathway: N, S, NS  HRR: Oxygraph-2k