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Mechanisms of cell injury by activated oxygen species.

Current evidence suggests that O2- and H2O2 injure cells as a result of the generation of a more potent oxidizing species. In addition to O2- and H2O2, the third essential component of the complex that mediates the lethal cell injury is a cellular source of ferric iron. The hypothesis most consisten...

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Detalles Bibliográficos
Autor principal: Farber, J L
Formato: Texto
Lenguaje:English
Publicado: 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566984/
https://www.ncbi.nlm.nih.gov/pubmed/7705293
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author Farber, J L
author_facet Farber, J L
author_sort Farber, J L
collection PubMed
description Current evidence suggests that O2- and H2O2 injure cells as a result of the generation of a more potent oxidizing species. In addition to O2- and H2O2, the third essential component of the complex that mediates the lethal cell injury is a cellular source of ferric iron. The hypothesis most consistent with all the available data suggests that O2- reduces a cellular source of ferric to ferrous iron, and the latter then reacts with H2O2 to produce a more potent oxidizing species, like the .OH or an equivalently reactive species. In turn, .OH initiates the peroxidative decomposition of the phospholipids of cellular membranes. .OH also damages the inner mitochondrial membrane. Upon mitochondrial deenergization, a sequence of events is initiated that similarly leads to the loss of viability of the cell. DNA represents a third cellular target of .OH. Depending on the cell type, oxidative DNA damage can be coupled to cell killing through a mechanism related to the activation of poly (ADP-ribose) polymerase.
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spelling pubmed-15669842006-09-19 Mechanisms of cell injury by activated oxygen species. Farber, J L Environ Health Perspect Research Article Current evidence suggests that O2- and H2O2 injure cells as a result of the generation of a more potent oxidizing species. In addition to O2- and H2O2, the third essential component of the complex that mediates the lethal cell injury is a cellular source of ferric iron. The hypothesis most consistent with all the available data suggests that O2- reduces a cellular source of ferric to ferrous iron, and the latter then reacts with H2O2 to produce a more potent oxidizing species, like the .OH or an equivalently reactive species. In turn, .OH initiates the peroxidative decomposition of the phospholipids of cellular membranes. .OH also damages the inner mitochondrial membrane. Upon mitochondrial deenergization, a sequence of events is initiated that similarly leads to the loss of viability of the cell. DNA represents a third cellular target of .OH. Depending on the cell type, oxidative DNA damage can be coupled to cell killing through a mechanism related to the activation of poly (ADP-ribose) polymerase. 1994-12 /pmc/articles/PMC1566984/ /pubmed/7705293 Text en
spellingShingle Research Article
Farber, J L
Mechanisms of cell injury by activated oxygen species.
title Mechanisms of cell injury by activated oxygen species.
title_full Mechanisms of cell injury by activated oxygen species.
title_fullStr Mechanisms of cell injury by activated oxygen species.
title_full_unstemmed Mechanisms of cell injury by activated oxygen species.
title_short Mechanisms of cell injury by activated oxygen species.
title_sort mechanisms of cell injury by activated oxygen species.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566984/
https://www.ncbi.nlm.nih.gov/pubmed/7705293
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