Malinska 2010 Biochim Biophys Acta: Difference between revisions
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{{Publication | {{Publication | ||
|title=Malinska D, Kulawiak B, Kudin AP, Kovacs R, Huchzermeyer C, Kann O, Szewczyk A, Kunz WS (2010) Complex III-dependent superoxide production of brain mitochondria contributes to seizure-related ROS formation. Biochim Biophys Acta 1797: 1163- | |title=Malinska D, Kulawiak B, Kudin AP, Kovacs R, Huchzermeyer C, Kann O, Szewczyk A, Kunz WS (2010) Complex III-dependent superoxide production of brain mitochondria contributes to seizure-related ROS formation. Biochim Biophys Acta 1797:1163-70. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed/20211146 PMID:20211146] | |info=[http://www.ncbi.nlm.nih.gov/pubmed/20211146 PMID: 20211146 Open Access] | ||
|authors=Malinska D, Kulawiak B, Kudin AP, Kovacs R, Huchzermeyer C, Kann O, Szewczyk A, Kunz WS | |authors=Malinska D, Kulawiak B, Kudin AP, Kovacs R, Huchzermeyer C, Kann O, Szewczyk A, Kunz WS | ||
|year=2010 | |year=2010 | ||
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is the direct electron donor for oxygen reduction in complex III-dependent superoxide production. Therefore, we conclude that under conditions of increased energy load the complex III site can contribute to superoxide | is the direct electron donor for oxygen reduction in complex III-dependent superoxide production. Therefore, we conclude that under conditions of increased energy load the complex III site can contribute to superoxide | ||
production of brain mitochondria, which might be relevant for epilepsy-related seizure activity. | production of brain mitochondria, which might be relevant for epilepsy-related seizure activity. | ||
|keywords= | |keywords=Reactive oxygen species, Brain mitochondria, Epilepsy | ||
|mipnetlab= | |mipnetlab=PL Warsaw Szewczyk A | ||
}} | }} | ||
{{Labeling | {{Labeling | ||
|organism=Mouse, Rat | |||
|tissues=Nervous system | |||
|preparations=Isolated mitochondria | |||
|injuries=Oxidative stress;RONS | |||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
}} | }} |
Latest revision as of 16:43, 19 March 2015
Malinska D, Kulawiak B, Kudin AP, Kovacs R, Huchzermeyer C, Kann O, Szewczyk A, Kunz WS (2010) Complex III-dependent superoxide production of brain mitochondria contributes to seizure-related ROS formation. Biochim Biophys Acta 1797:1163-70. |
Malinska D, Kulawiak B, Kudin AP, Kovacs R, Huchzermeyer C, Kann O, Szewczyk A, Kunz WS (2010) Biochim Biophys Acta
Abstract: Brain seizure activity is characterised by intense activation of mitochondrial oxidative phosphorylation. This stimulation of oxidative phosphorylation is in the low magnesium model of seizure-like events accompanied by substantial increase in formation of reactive oxygen species (ROS). However, it has remained unclearwhich ROSgenerating sites can be attributed to this phenomenon. Here, we report stimulatory effects of calcium ions and uncouplers, mimickingmitochondrial activation, on ROS generation of isolated rat andmouse brainmitochondria. Since these stimulatory effectswere visiblewith superoxide sensitive dyes, butwith hydrogen peroxide sensitive dyes only in the additional presence of SOD, we conclude that the complex redox properties of the โQoโ center at respiratory chain complex III are very likely responsible for these observations. In accordancewith this hypothesis redox titrations of the superoxide production of antimycin-inhibited submitochondrial particles with the succinate/fumarate redox couple confirmed for brain tissue a bell-shapeddependencywith amaximal superoxide production rate at+10 mV(pH=7.4). This reflects the complex redox properties of a semiquinone specieswhich is the direct electron donor for oxygen reduction in complex III-dependent superoxide production. Therefore, we conclude that under conditions of increased energy load the complex III site can contribute to superoxide production of brain mitochondria, which might be relevant for epilepsy-related seizure activity. โข Keywords: Reactive oxygen species, Brain mitochondria, Epilepsy
โข O2k-Network Lab: PL Warsaw Szewczyk A
Labels:
Stress:Oxidative stress;RONS Organism: Mouse, Rat Tissue;cell: Nervous system Preparation: Isolated mitochondria
HRR: Oxygraph-2k