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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1995-9-19
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pubmed:abstractText |
Studies were undertaken to investigate the hypothesis that infiltrating glomerular macrophages in experimental glomerulonephritis are activated to produce oxygen-free radicals that are capable of enhancing oxidation of low-density lipoprotein (LDL). Low-density lipoprotein oxidation was assessed by increased electrophoretic mobility on agarose gel electrophoresis and by the generation of thiobarbituric acid-reactive substances. Lipoprotein uptake, degradation, and re-esterification by macrophages were assessed by measuring 14C-oleic acid incorporation into cholesteryl oleate. Both peritoneal and glomerular macrophages have the ability to oxidize LDL to a form showing increased mobility on agarose gel electrophoresis. However, LDL incubated with glomerular macrophages underwent greater oxidation, resulting in increased generation of thiobarbituric acid-reactive substances (15.1 +/- 1.2 nmol malondialdehyde/mg LDL protein v 7.2 +/- 2.1 nmol malondialdehyde/mg LDL protein; P < 0.01). In addition, glomerular macrophages modified LDL to a form that greatly enhanced cellular synthesis of cholesteryl oleate compared with peritoneal macrophage-modified LDL (30 +/- 11 pmol/10(6) cells/hr v 10 +/- 4 pmol/10(6) cells/hr; P < 0.01). Superoxide dismutase, a scavenger of superoxide anion, inhibited macrophage-mediated oxidation of LDL. These results suggest that glomerular macrophages from nephritic rats are activated to modify LDL to a form avidly taken up by macrophage scavenger receptors. Thus, enhanced formation of oxidized LDL by infiltrating glomerular macrophages may contribute to glomerular injury in nephrotoxic serum nephritis.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol Esters,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoproteins, LDL,
http://linkedlifedata.com/resource/pubmed/chemical/Oleic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Oleic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Thiobarbituric Acid Reactive...,
http://linkedlifedata.com/resource/pubmed/chemical/cholesteryl oleate
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0272-6386
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
362-7
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:7645542-Animals,
pubmed-meshheading:7645542-Cholesterol Esters,
pubmed-meshheading:7645542-Electrophoresis, Agar Gel,
pubmed-meshheading:7645542-Glomerulonephritis,
pubmed-meshheading:7645542-Kidney Glomerulus,
pubmed-meshheading:7645542-Lipoproteins, LDL,
pubmed-meshheading:7645542-Macrophage Activation,
pubmed-meshheading:7645542-Macrophages,
pubmed-meshheading:7645542-Macrophages, Peritoneal,
pubmed-meshheading:7645542-Male,
pubmed-meshheading:7645542-Oleic Acid,
pubmed-meshheading:7645542-Oleic Acids,
pubmed-meshheading:7645542-Oxidation-Reduction,
pubmed-meshheading:7645542-Rats,
pubmed-meshheading:7645542-Rats, Sprague-Dawley,
pubmed-meshheading:7645542-Thiobarbituric Acid Reactive Substances
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pubmed:year |
1995
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pubmed:articleTitle |
Glomerular macrophages in nephrotoxic serum nephritis are activated to oxidize low-density lipoprotein.
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pubmed:affiliation |
Department of Medicine, Montefiore Medical Center, Bronx, NY, USA.
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pubmed:publicationType |
Journal Article
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