Source:http://linkedlifedata.com/resource/pubmed/id/11779401
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
18
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pubmed:dateCreated |
2002-1-7
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pubmed:abstractText |
The purpose of this study was to investigate the effectiveness of superoxide dismutase (SOD) overexpression in an acute model of hepatic oxidative stress. Oxidative stress was established using a warm ischemia-reperfusion model, where nearly 70% of the liver was made hypoxic by clamping the hepatic artery and a branch of the portal vein for 1 hr followed by restoration of blood flow. Animals were infected i.v. with 1 x 10(9) plaque-forming units (PFU) of adenovirus containing the transgene for cytosolic Cu/Zn-SOD (Ad.SOD1), mitochondrial Mn-SOD (Ad.SOD2), extracellular Cu/Zn-SOD (Ad.SOD3), or the bacterial reporter gene for beta-galactosidase (Ad.lacZ) 3 days prior to experiments. Ad.SOD1 and Ad.SOD2 caused a three-fold increase in SOD expression and activity in liver compared to Ad.lacZ-treated control animals. Intravenous administration of Ad.SOD3 increased SOD activity slightly in serum but not in liver. Increases in serum transaminases and pathology due to ischemia-reperfusion were blunted by Ad.SOD1 and Ad.SOD2; however, extracellular SOD had no significant effect. Moreover, lipid-derived free radical adducts (a(N) = 15.65 G and a(H)(beta) = 2.78 G) were increased by ischemia-reperfusion. This effect was blunted by about 60% in Ad.SOD1- and Ad.SOD2-infected animals, but was unaffected by Ad.SOD3. However, when high doses of Ad.SOD3 (3 x 10(10) PFU) were administered. serum SOD activity was elevated three-fold and was protective against hepatic ischemia-reperfusion injury under these conditions. These data demonstrate that adenoviral delivery of superoxide dismutase can effectively reduce hepatic oxidative stress.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1043-0342
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
10
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2167-77
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11779401-Adenoviruses, Human,
pubmed-meshheading:11779401-Animals,
pubmed-meshheading:11779401-Free Radicals,
pubmed-meshheading:11779401-Gene Expression,
pubmed-meshheading:11779401-Gene Transfer Techniques,
pubmed-meshheading:11779401-Genetic Vectors,
pubmed-meshheading:11779401-Humans,
pubmed-meshheading:11779401-Isoenzymes,
pubmed-meshheading:11779401-Liver,
pubmed-meshheading:11779401-Oxidative Stress,
pubmed-meshheading:11779401-Rats,
pubmed-meshheading:11779401-Rats, Sprague-Dawley,
pubmed-meshheading:11779401-Reperfusion Injury,
pubmed-meshheading:11779401-Superoxide Dismutase
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pubmed:year |
2001
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pubmed:articleTitle |
Comparison of the effect of adenoviral delivery of three superoxide dismutase genes against hepatic ischemia-reperfusion injury.
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pubmed:affiliation |
Department of Pharmacology and Center for Alcohol Studies, CB #7365 Mary Ellen Jones Bldg., University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. wheelmi@med.unc.edu
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.
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