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Influence of Nitric Oxide on Cellular and Mitochondrial Integrity in Oxidatively Stressed Astrocytes
Astrocytes provide protection and trophic support to neurons, but like neurons are vulnerable to oxidative stress. Decreased function of astrocytes resulting from oxidative stress could contribute to neurodegeneration. Our goal is to understand the intracellular events associated with oxidative stre...
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Published in: | Journal of neuroscience research 1999-04, Vol.56 (2), p.166-176 |
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container_title | Journal of neuroscience research |
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creator | Robb, S J Gaspers, L D Wright, K J Thomas, AP Connor, J R |
description | Astrocytes provide protection and trophic support to neurons, but like neurons are vulnerable to oxidative stress. Decreased function of astrocytes resulting from oxidative stress could contribute to neurodegeneration. Our goal is to understand the intracellular events associated with oxidative stress in astrocytes. Because nitric oxide (NO super(.)) has been implicated as a contributor to oxidative stress in the brain, we examined in this study whether NO super(.) contributed to oxidative stress in astrocytes. Stimulation of NO super(.) decreases superoxide levels, preserves mitochondrial membrane potential, and decreases mitochondrial swelling in astrocytes treated with peroxide. Chelation of NO super(.) is associated with increased cell death, mitochondrial swelling, and loss of mitochondrial membrane potential, in response to peroxide treatment. Peroxide treatment increased intracellular calcium and the peroxide-induced changes in intracellular calcium were not altered in response to NO super(.). Iron-loading increases peroxide-induced oxidative stress in astrocytes, but induction of NO super(.) limited the iron effect, suggesting an interaction between iron and NO super(.). These data suggest endogenously produced NO super(.) protects astrocytes from oxidative stress, perhaps by preserving mitochondrial function. |
doi_str_mv | 10.1002/(SICI)1097-4547(19990415)56:2<166::AID-JNR6>3.3.CO;2-J |
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Decreased function of astrocytes resulting from oxidative stress could contribute to neurodegeneration. Our goal is to understand the intracellular events associated with oxidative stress in astrocytes. Because nitric oxide (NO super(.)) has been implicated as a contributor to oxidative stress in the brain, we examined in this study whether NO super(.) contributed to oxidative stress in astrocytes. Stimulation of NO super(.) decreases superoxide levels, preserves mitochondrial membrane potential, and decreases mitochondrial swelling in astrocytes treated with peroxide. Chelation of NO super(.) is associated with increased cell death, mitochondrial swelling, and loss of mitochondrial membrane potential, in response to peroxide treatment. Peroxide treatment increased intracellular calcium and the peroxide-induced changes in intracellular calcium were not altered in response to NO super(.). Iron-loading increases peroxide-induced oxidative stress in astrocytes, but induction of NO super(.) limited the iron effect, suggesting an interaction between iron and NO super(.). 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Decreased function of astrocytes resulting from oxidative stress could contribute to neurodegeneration. Our goal is to understand the intracellular events associated with oxidative stress in astrocytes. Because nitric oxide (NO super(.)) has been implicated as a contributor to oxidative stress in the brain, we examined in this study whether NO super(.) contributed to oxidative stress in astrocytes. Stimulation of NO super(.) decreases superoxide levels, preserves mitochondrial membrane potential, and decreases mitochondrial swelling in astrocytes treated with peroxide. Chelation of NO super(.) is associated with increased cell death, mitochondrial swelling, and loss of mitochondrial membrane potential, in response to peroxide treatment. Peroxide treatment increased intracellular calcium and the peroxide-induced changes in intracellular calcium were not altered in response to NO super(.). Iron-loading increases peroxide-induced oxidative stress in astrocytes, but induction of NO super(.) limited the iron effect, suggesting an interaction between iron and NO super(.). 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Iron-loading increases peroxide-induced oxidative stress in astrocytes, but induction of NO super(.) limited the iron effect, suggesting an interaction between iron and NO super(.). These data suggest endogenously produced NO super(.) protects astrocytes from oxidative stress, perhaps by preserving mitochondrial function.</abstract><doi>10.1002/(SICI)1097-4547(19990415)56:2<166::AID-JNR6>3.3.CO;2-J</doi><tpages>11</tpages></addata></record> |
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title | Influence of Nitric Oxide on Cellular and Mitochondrial Integrity in Oxidatively Stressed Astrocytes |
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