pubmed-article:9717976 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C0025926 | lld:lifeskim |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C1704256 | lld:lifeskim |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C0022663 | lld:lifeskim |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C0178664 | lld:lifeskim |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C1533698 | lld:lifeskim |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C0205216 | lld:lifeskim |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C1515406 | lld:lifeskim |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C1515670 | lld:lifeskim |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C0392756 | lld:lifeskim |
pubmed-article:9717976 | lifeskim:mentions | umls-concept:C0282774 | lld:lifeskim |
pubmed-article:9717976 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:9717976 | pubmed:dateCreated | 1998-9-9 | lld:pubmed |
pubmed-article:9717976 | pubmed:abstractText | Over-expression of iNOS is implicated in the pathogenesis of glomerulonephritis in animal models of systemic lupus erythematosus. The aim of this study was to evaluate the effect of aminoguanidine, a selective inhibitor of iNOS, for the protection from glomerulosclerosis in NZB/W F1 mice. Female NZB/W F1 mice (n = 8) were treated with aminoguanidine (1 g/l) in drinking water for 4 months starting at age 2 months before the onset of glomerulonephritis. Controls were age- and sex-matched mice (n = 10) without aminoguanidine treatment. By glomerular microdissection and reverse-transcription competitive polymerase chain reaction, we found that glomerular iNOS/beta-actin and TGF-beta1/beta-actin mRNA ratios were reduced 15.1% (P<0.05) and 61.3% (P<0.01), respectively, in aminoguanidine-treated mice. Aminoguanidine significantly reduced the glomerular iNOS staining, urinary nitrite production and degree of glomerulosclerosis. In addition, the glomerular volume and mean glomerular cell number were reduced 33.2% (P<0.01) and 32.8% (P<0.01), respectively. Likewise, the urinary proteinuria was also significantly reduced by aminoguanidine. These results indicate that administration of aminoguanidine may reduce the progression of glomerulosclerosis in NZB/W F1 mice, possibly through inhibition of glomerular nitric oxide production. | lld:pubmed |
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pubmed-article:9717976 | pubmed:language | eng | lld:pubmed |
pubmed-article:9717976 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9717976 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:9717976 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9717976 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:9717976 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9717976 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9717976 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:9717976 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9717976 | pubmed:month | Aug | lld:pubmed |
pubmed-article:9717976 | pubmed:issn | 0009-9104 | lld:pubmed |
pubmed-article:9717976 | pubmed:author | pubmed-author:YuC CCC | lld:pubmed |
pubmed-article:9717976 | pubmed:author | pubmed-author:HuangC CCC | lld:pubmed |
pubmed-article:9717976 | pubmed:author | pubmed-author:OhY HYH | lld:pubmed |
pubmed-article:9717976 | pubmed:author | pubmed-author:YangC WCW | lld:pubmed |
pubmed-article:9717976 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9717976 | pubmed:volume | 113 | lld:pubmed |
pubmed-article:9717976 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9717976 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9717976 | pubmed:pagination | 258-64 | lld:pubmed |
pubmed-article:9717976 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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