Tretter 2012 Free Radic Biol Med: Difference between revisions

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{{Publication
{{Publication
|title=Tretter L, Adam-Vizi V. (2012) High Ca2+ load promotes hydrogen peroxide generation via activation of ฮฑ-glycerophosphate dehydrogenase in brain mitochondria.. Free Radic Biol Med 53(11):2119-30. ย 
|title=Tretter L, Adam-Vizi V. (2012) High Ca2+ load promotes hydrogen peroxide generation via activation of ฮฑ-glycerophosphate dehydrogenase in brain mitochondria.. Free Radic Biol Med 53(11):2119-30.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/23022874]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/23022874 PMID: 23022874]
|authors=Tretter L, Adam-Vizi V.
|authors=Tretter L, Adam-Vizi V.
|year=2012
|year=2012

Revision as of 14:06, 19 February 2013

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Tretter L, Adam-Vizi V. (2012) High Ca2+ load promotes hydrogen peroxide generation via activation of ฮฑ-glycerophosphate dehydrogenase in brain mitochondria.. Free Radic Biol Med 53(11):2119-30.

ยป PMID: 23022874

Tretter L, Adam-Vizi V. (2012) Free Radic Biol Med

Abstract: H(2)O(2) generation associated with ฮฑ-glycerophosphate (ฮฑ-GP) oxidation was addressed in guinea pig brain mitochondria challenged with high Ca(2+) load (10 ฮผM). Exposure to 10 ฮผM Ca(2+) induced an abrupt 2.5-fold increase in H(2)O(2) release compared to that measured in the presence of a physiological cytosolic Ca(2+) concentration (100 nM) from mitochondria respiring on 5 mM ฮฑ-GP in the presence of ADP (2 mM). The Ca(2+)-induced stimulation of H(2)O(2) generation was reversible and unaltered by the uniporter blocker Ru 360, indicating that it did not require Ca(2+) uptake into mitochondria. Enhanced H(2)O(2) generation by Ca(2+) was also observed in the absence of ADP when mitochondria exhibited permeability transition pore opening with a decrease in the NAD(P)H level, dissipation of membrane potential, and mitochondrial swelling. Furthermore, mitochondria treated with the pore-forming peptide alamethicin also responded with an elevated H(2)O(2) generation to a challenge with 10 ฮผM Ca(2+). Ca(2+)-induced promotion of H(2)O(2) formation was further enhanced by the complex III inhibitor myxothiazol. With 20 mM ฮฑ-GP concentration, stimulation of H(2)O(2) formation by Ca(2+) was detected only in the presence, not in the absence, of ADP. It is concluded that ฮฑ-glycerophosphate dehydrogenase, which is accessible to and could be activated by a rise in the level of cytosolic Ca(2+), makes a major contribution to Ca(2+)-stimulated H(2)O(2) generation. This work highlights a unique high-Ca(2+)-stimulated reactive oxygen species-forming mechanism in association with oxidation of ฮฑ-GP, which is largely independent of the bioenergetic state and can proceed even in damaged, functionally incompetent mitochondria. โ€ข Keywords: Mitochondria; Reactive oxygen species; Calcium; Hydrogen peroxide; ฮฑ-Glycerophosphate dehydrogenase; Reverse electron transport; Permeability transition pore; Myxothiazol; ฮฑ-Glycerophosphate shuttle; Free radicals

โ€ข O2k-Network Lab: HU_Budapest_Tretter L, HU Budapest Semmelweis Univ


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