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Prolonged Administration Enhances the Renoprotective Effect of Pentoxifylline via Anti-Inflammatory Activity in Streptozotocin-Induced Diabetic Nephropathy

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dc.contributor.authorHan, Kum Hyun-
dc.contributor.authorHan, Sang Youb-
dc.contributor.authorKim, Han Seong-
dc.contributor.authorKang, Young Sun-
dc.contributor.authorCha, Dae Ryong-
dc.date.available2020-11-03T05:51:12Z-
dc.date.issued2010-06-
dc.identifier.issn0360-3997-
dc.identifier.issn1573-2576-
dc.identifier.urihttps://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/14835-
dc.description.abstractThe beneficial effects of pentoxifylline (PTX), which has an anti-inflammatory and renoprotective effect in diabetic nephropathy, are not completely understood. This study investigates whether prolonged administration of PTX (40 mg/kg, per oral) is effective in streptozotocin-induced diabetic nephropathy. The amount of urinary protein was higher in the diabetic rats than in the control rats. The amount remained unchanged after 4 weeks and decreased after 8 weeks of PTX treatment. Accumulation of monocyte chemoattractant peptide-1 (MCP-1) and mouse monoclonal anti-monocyte/macrophage antibody (ED-1) positive cells was higher in untreated diabetic rats than in the control rats. PTX administration ameliorated the urinary MCP-1 excretion and interstitial infiltration of ED-1 positive cells at 4 weeks. Further, in diabetic rats, administration of PTX for 4 weeks inhibited the renal inflammatory reaction, and when administration for 8 weeks, it prevented proteinuria. These findings support the hypothesis that prolonged administration enhances the protective effects of PTX.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherSPRINGER/PLENUM PUBLISHERS-
dc.titleProlonged Administration Enhances the Renoprotective Effect of Pentoxifylline via Anti-Inflammatory Activity in Streptozotocin-Induced Diabetic Nephropathy-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1007/s10753-009-9167-6-
dc.identifier.scopusid2-s2.0-77954691093-
dc.identifier.wosid000276870900001-
dc.identifier.bibliographicCitationINFLAMMATION, v.33, no.3, pp 137 - 143-
dc.citation.titleINFLAMMATION-
dc.citation.volume33-
dc.citation.number3-
dc.citation.startPage137-
dc.citation.endPage143-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusMONOCYTE CHEMOATTRACTANT PROTEIN-1-
dc.subject.keywordPlusCONVERTING ENZYME-INHIBITION-
dc.subject.keywordPlusTUMOR-NECROSIS-FACTOR-
dc.subject.keywordPlusURINARY PROTEIN-
dc.subject.keywordPlusGENE-THERAPY-
dc.subject.keywordPlusRENAL INJURY-
dc.subject.keywordPlusSHORT-TERM-
dc.subject.keywordPlusRATS-
dc.subject.keywordPlusPROGRESSION-
dc.subject.keywordPlusCOMPLICATIONS-
dc.subject.keywordAuthordiabetic nephropathy-
dc.subject.keywordAuthorinflammation-
dc.subject.keywordAuthorpentoxifylline-
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