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Difference between revisions of "Gnaiger 2001 Respir Physiol"

From Bioblast
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|keywords=Energy: Oxidative phosphorylation, Adenosine diphosphate kinetics, Adenosine diphosphate/O<sub>2</sub> ratio; Hypoxia: Mitochondrial O<sub>2</sub> kinetics, Mammals: Rat, Membrane permeability, Mitochondria: Heart, Liver
|keywords=Energy: Oxidative phosphorylation, Adenosine diphosphate kinetics, Adenosine diphosphate/O<sub>2</sub> ratio; Hypoxia: Mitochondrial O<sub>2</sub> kinetics, Mammals: Rat, Membrane permeability, Mitochondria: Heart, Liver
|mipnetlab=AT Innsbruck Gnaiger E
|mipnetlab=AT Innsbruck Gnaiger E
|articletype=Protocol; Manual
|discipline=Mitochondrial Physiology
}}
}}
[[File:Gnaiger 2001 Respir Physiol New Fig10.jpg|255px|left|thumb|link=]]
'''Fig. 10''' (modified): Opposite effects of ADP limitation and oxygen limitation on mitochondrial membrane potential, and [[LEAK respiration|LEAK oxygen flux]], ''J''<sub>O2,''L''</sub>. The LEAK state is obtained when total oxygen flux equals LEAK respiration. In all other [[respiratory state]]s, total oxygen flux is the sum of LEAK oxygen flux and mechanistically coupled oxygen flux. '''A''': ADP limitation of respiration at high oxygen levels in the transition from the [[OXPHOS]] state (''P'', saturating ADP) or active [[State 3]] (high ADP) to the resting LEAK state, ''L'' (compare [[State 4]]), leads to an increase of membrane potential and exponential acceleration of the proton leak (heavy line). Because LEAK oxygen flux increases while total oxygen flux is reduced, the [[ATP yield]] (ADP/O<sub>2</sub> flux ratio) declines to zero. Turnover-dependent proton leak increases the LEAK oxygen flux in the OXPHOS state but declines towards the LEAK state ([[Garlid_1993_BTK|Garlid et al 1993]]). Mitochondrial production of reactive oxygen species (ROS) increases with membrane potential towards the LEAK state, and ROS-linked electron bypass (electron leak) contributes minimally to LEAK oxygen flux at high oxygen ([[Gnaiger 2000 Proc Natl Acad Sci U S A|Gnaiger et al 2000]]). On the right, the decline of ~P/O<sub>2</sub> flux ratios is shown in the transition from OXPHOS to LEAK.Β  '''B''': Oxygen limitation of respiration causes a reduction of membrane potential in the transition from ADP limitation at high oxygen, to intracellular conditions of low oxygen and low ADP, to finally severe oxygen limitation under hypoxia and anoxia. Potentially synergistic with the well documented membrane potential effect on LEAK flux, are the hypothetical effects of decreasing membrane permeability and suppression of ROS production under severe hypoxia, whereas intermediary levels of hypoxia may increase ROS production (modified from Gnaiger 2001; see original publication for further references).
* Discussion: [[Permeabilized_muscle_fibers#Oxygen_dependence_of_ROS_production_-_are_permeabilized_fibers_a_valid_model.3F|'''Oxygen dependence of ROS production - are permeabilized fibers a valid model?''']].
{{Labeling
{{Labeling
|area=Respiration, Instruments;methods, Comparative MiP;environmental MiP
|area=Respiration, Instruments;methods, Comparative MiP;environmental MiP
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|topics=ADP, Coupling efficiency;uncoupling, Oxygen kinetics, Threshold;excess capacity
|topics=ADP, Coupling efficiency;uncoupling, Oxygen kinetics, Threshold;excess capacity
|couplingstates=OXPHOS
|couplingstates=OXPHOS
|instruments=Oxygraph-2k, TIP2k
|instruments=Oxygraph-2k, TIP2k, ADP, ATP
|articletype=Protocol; Manual
|discipline=Mitochondrial Physiology
}}
}}
[[File:Gnaiger 2001 Respir Physiol New Fig10.jpg|255px|left|thumb|link=]]
'''Fig. 10''' (modified): Opposite effects of ADP limitation and oxygen limitation on mitochondrial membrane potential, and [[LEAK respiration|LEAK oxygen flux]], ''J''<sub>O2,''L''</sub>. The LEAK state is obtained when total oxygen flux equals LEAK respiration. In all other [[respiratory state]]s, total oxygen flux is the sum of LEAK oxygen flux and mechanistically coupled oxygen flux. '''A''': ADP limitation of respiration at high oxygen levels in the transition from the [[OXPHOS]] state (''P'', saturating ADP) or active [[State 3]] (high ADP) to the resting LEAK state, ''L'' (compare [[State 4]]), leads to an increase of membrane potential and exponential acceleration of the proton leak (heavy line). Because LEAK oxygen flux increases while total oxygen flux is reduced, the [[ATP yield]] (ADP/O<sub>2</sub> flux ratio) declines to zero. Turnover-dependent proton leak increases the LEAK oxygen flux in the OXPHOS state but declines towards the LEAK state ([[Garlid_1993_BTK|Garlid et al 1993]]). Mitochondrial production of reactive oxygen species (ROS) increases with membrane potential towards the LEAK state, and ROS-linked electron bypass (electron leak) contributes minimally to LEAK oxygen flux at high oxygen ([[Gnaiger 2000 Proc Natl Acad Sci U S A|Gnaiger et al 2000]]). On the right, the decline of ~P/O<sub>2</sub> flux ratios is shown in the transition from OXPHOS to LEAK.Β  '''B''': Oxygen limitation of respiration causes a reduction of membrane potential in the transition from ADP limitation at high oxygen, to intracellular conditions of low oxygen and low ADP, to finally severe oxygen limitation under hypoxia and anoxia. Potentially synergistic with the well documented membrane potential effect on LEAK flux, are the hypothetical effects of decreasing membrane permeability and suppression of ROS production under severe hypoxia, whereas intermediary levels of hypoxia may increase ROS production (modified from Gnaiger 2001; see original publication for further references).
* Discussion: [[Permeabilized_muscle_fibers#Oxygen_dependence_of_ROS_production_-_are_permeabilized_fibers_a_valid_model.3F|'''Oxygen dependence of ROS production - are permeabilized fibers a valid model?''']].

Revision as of 14:20, 27 May 2020

Publications in the MiPMap
Gnaiger E (2001) Bioenergetics at low oxygen: dependence of respiration and phosphorylation on oxygen and adenosine diphosphate supply. Respir Physiol 128:277-97.

Β» PMID: 11718759, Bioblast pdf

Gnaiger E (2001) Respir Physiol

Abstract: Oxygen limitation is generally considered as impairment of mitochondrial respiration under hypoxia and ischemia. Low intracellular oxygen levels under normoxia, however, imply mild oxygen limitation, provide protection from oxidative stress, and result from economical strategies for oxygen transport through the respiratory cascade to cytochrome c oxidase. Both perspectives relate to the critical oxygen pressure which inhibits mitochondrial respiration. Based on methodological considerations of oxygen kinetics and a presentation of high-resolution respirometry, mitochondrial oxygen affinities (1/p50) are reviewed with particular emphasis on the turnover effect under control of ADP, which increases the p2 in active states. ~P/O2 flux ratios are high even under severe oxygen limitation, as demonstrated by calorespirometry. Oxygen limitation reduces the uncoupled respiration observed under control by ADP, as shown by relationships derived between ~P/O2 flux ratios, respiratory control ratios, and ADP kinetics. Bioenergetics at low oxygen versus oxidative stress must be considered in the context of limitation of maximum aerobic activity, ischemia-reperfusion injury, mitochondrial signalling to apoptosis, and mitochondrial theories of ageing. β€’ Keywords: Energy: Oxidative phosphorylation, Adenosine diphosphate kinetics, Adenosine diphosphate/O2 ratio; Hypoxia: Mitochondrial O2 kinetics, Mammals: Rat, Membrane permeability, Mitochondria: Heart, Liver

β€’ O2k-Network Lab: AT Innsbruck Gnaiger E

Gnaiger 2001 Respir Physiol New Fig10.jpg

Fig. 10 (modified): Opposite effects of ADP limitation and oxygen limitation on mitochondrial membrane potential, and LEAK oxygen flux, JO2,L. The LEAK state is obtained when total oxygen flux equals LEAK respiration. In all other respiratory states, total oxygen flux is the sum of LEAK oxygen flux and mechanistically coupled oxygen flux. A: ADP limitation of respiration at high oxygen levels in the transition from the OXPHOS state (P, saturating ADP) or active State 3 (high ADP) to the resting LEAK state, L (compare State 4), leads to an increase of membrane potential and exponential acceleration of the proton leak (heavy line). Because LEAK oxygen flux increases while total oxygen flux is reduced, the ATP yield (ADP/O2 flux ratio) declines to zero. Turnover-dependent proton leak increases the LEAK oxygen flux in the OXPHOS state but declines towards the LEAK state (Garlid et al 1993). Mitochondrial production of reactive oxygen species (ROS) increases with membrane potential towards the LEAK state, and ROS-linked electron bypass (electron leak) contributes minimally to LEAK oxygen flux at high oxygen (Gnaiger et al 2000). On the right, the decline of ~P/O2 flux ratios is shown in the transition from OXPHOS to LEAK. B: Oxygen limitation of respiration causes a reduction of membrane potential in the transition from ADP limitation at high oxygen, to intracellular conditions of low oxygen and low ADP, to finally severe oxygen limitation under hypoxia and anoxia. Potentially synergistic with the well documented membrane potential effect on LEAK flux, are the hypothetical effects of decreasing membrane permeability and suppression of ROS production under severe hypoxia, whereas intermediary levels of hypoxia may increase ROS production (modified from Gnaiger 2001; see original publication for further references).

* Discussion: Oxygen dependence of ROS production - are permeabilized fibers a valid model?.


Labels: MiParea: Respiration, Instruments;methods, Comparative MiP;environmental MiP 

Stress:Oxidative stress;RONS  Organism: Human, Rat  Tissue;cell: Heart, Liver, Endothelial;epithelial;mesothelial cell, HUVEC  Preparation: Intact cells, Isolated mitochondria 

Regulation: ADP, Coupling efficiency;uncoupling, Oxygen kinetics, Threshold;excess capacity  Coupling state: OXPHOS 

HRR: Oxygraph-2k, TIP2k, ADP"ADP" is not in the list (Oxygraph-2k, TIP2k, O2k-Fluorometer, pH, NO, TPP, Ca, O2k-Spectrophotometer, O2k-Manual, O2k-Protocol, ...) of allowed values for the "Instrument and method" property., ATP"ATP" is not in the list (Oxygraph-2k, TIP2k, O2k-Fluorometer, pH, NO, TPP, Ca, O2k-Spectrophotometer, O2k-Manual, O2k-Protocol, ...) of allowed values for the "Instrument and method" property.