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Characteristics of alpha-glycerophosphate-evoked H2O2 generation in brain mitochondria.
- Source :
-
Journal of neurochemistry [J Neurochem] 2007 Feb; Vol. 100 (3), pp. 650-63. - Publication Year :
- 2007
-
Abstract
- Characteristics of reactive oxygen species (ROS) production in isolated guinea-pig brain mitochondria respiring on alpha-glycerophosphate (alpha-GP) were investigated and compared with those supported by succinate. Mitochondria established a membrane potential (DeltaPsi(m)) and released H(2)O(2) in parallel with an increase in NAD(P)H fluorescence in the presence of alpha-GP (5-40 mm). H(2)O(2) formation and the increase in NAD(P)H level were inhibited by rotenone, ADP or FCCP, respectively, being consistent with a reverse electron transfer (RET). The residual H(2)O(2) formation in the presence of FCCP was stimulated by myxothiazol in mitochondria supported by alpha-GP, but not by succinate. ROS under these conditions are most likely to be derived from alpha-GP-dehydrogenase. In addition, huge ROS formation could be provoked by antimycin in alpha-GP-supported mitochondria, which was prevented by myxothiazol, pointing to the generation of ROS at the quinol-oxidizing center (Q(o)) site of complex III. FCCP further stimulated the production of ROS to the highest rate that we observed in this study. We suggest that the metabolism of alpha-GP leads to ROS generation primarily by complex I in RET, and in addition a significant ROS formation could be ascribed to alpha-GP-dehydrogenase in mammalian brain mitochondria. ROS generation by alpha-GP at complex III is evident only when this complex is inhibited by antimycin.
- Subjects :
- Animals
Antifungal Agents pharmacology
Antimycin A analogs & derivatives
Antimycin A pharmacology
Cell Respiration drug effects
Electron Transport drug effects
Electron Transport physiology
Electron Transport Complex I drug effects
Electron Transport Complex I metabolism
Electron Transport Complex III drug effects
Electron Transport Complex III metabolism
Glycerolphosphate Dehydrogenase drug effects
Glycerolphosphate Dehydrogenase metabolism
Guinea Pigs
Membrane Potential, Mitochondrial drug effects
Membrane Potential, Mitochondrial physiology
Methacrylates pharmacology
Mitochondria drug effects
NADP drug effects
NADP metabolism
Reactive Oxygen Species metabolism
Subcellular Fractions
Succinic Acid metabolism
Thiazoles pharmacology
Uncoupling Agents pharmacology
Brain metabolism
Cell Respiration physiology
Glycerophosphates metabolism
Hydrogen Peroxide metabolism
Mitochondria metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0022-3042
- Volume :
- 100
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of neurochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 17263793
- Full Text :
- https://doi.org/10.1111/j.1471-4159.2006.04223.x