Source:http://linkedlifedata.com/resource/pubmed/id/21291499
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2011-4-5
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pubmed:abstractText |
Epigallocatechin-3-gallate (EGCG) shows diverse chemical and biological activities. We investigated the effects of EGCG in a rat renal ischemia reperfusion (I/R) injury model. Sprague-Dawley rats received intraperitoneal injection of 50 mg/kg EGCG 48 h, 24 h, and 30 min prior to I/R injury. The animals were subjected to left renal occlusion for 45 min. EGCG treatment suppressed the peak in serum creatinine. EGCG-treated kidneys showed significantly less tubular damage and a decreased number of apoptotic cells. The I/R-induced elevation in the renal MDA level was significantly decreased in the EGCG group. Reverse-transcriptase polymerase chain reaction showed that EGCG significantly decreased the expression of MHC class II, TLR2, TLR4, MCP-1, IL-18, TGF-?1, procollagen Ia1, TIMP-1, and Kim-1. ED-1 staining showed reduced macrophage infiltration and ?-SMA staining revealed less interstitial expression. Heme oxygenase-1 (HO-1) expression in I/R kidneys was upregulated in the EGCG group based on the results of both RT-PCR and Western blotting analysis. Blockade of HO-1 gene induction by SnPP increased renal tubular damage and macrophage infiltration. These findings suggest that EGCG protects the kidneys against I/R injury by reducing macrophage infiltration and decreasing renal fibrosis. These beneficial effects may be mediated, in part, by augmentation of the HO-1 gene.
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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/Actins,
http://linkedlifedata.com/resource/pubmed/chemical/Catechin,
http://linkedlifedata.com/resource/pubmed/chemical/Heme Oxygenase (Decyclizing),
http://linkedlifedata.com/resource/pubmed/chemical/Hmox1 protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Malondialdehyde,
http://linkedlifedata.com/resource/pubmed/chemical/Organic Chemicals,
http://linkedlifedata.com/resource/pubmed/chemical/SYBR Green I,
http://linkedlifedata.com/resource/pubmed/chemical/epigallocatechin gallate
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1432-2277
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pubmed:author |
pubmed-author:AbeToyofumiT,
pubmed-author:HyonSuong-HyuSH,
pubmed-author:IchimaruNaotsuguN,
pubmed-author:IsakaYoshitakaY,
pubmed-author:KakutaYoichiY,
pubmed-author:MatsumuraKazuakiK,
pubmed-author:NonomuraNorioN,
pubmed-author:OkumiMasayoshiM,
pubmed-author:TakaharaShiroS,
pubmed-author:TsutaharaKoichiK,
pubmed-author:YazawaKojiK
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pubmed:copyrightInfo |
© 2011 The Authors. Transplant International © 2011 European Society for Organ Transplantation.
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pubmed:issnType |
Electronic
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
514-22
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pubmed:meshHeading |
pubmed-meshheading:21291499-Actins,
pubmed-meshheading:21291499-Animals,
pubmed-meshheading:21291499-Apoptosis,
pubmed-meshheading:21291499-Catechin,
pubmed-meshheading:21291499-Heme Oxygenase (Decyclizing),
pubmed-meshheading:21291499-Kidney,
pubmed-meshheading:21291499-Lipid Peroxidation,
pubmed-meshheading:21291499-Macrophages,
pubmed-meshheading:21291499-Malondialdehyde,
pubmed-meshheading:21291499-Muscle, Smooth,
pubmed-meshheading:21291499-Organic Chemicals,
pubmed-meshheading:21291499-Rats,
pubmed-meshheading:21291499-Rats, Sprague-Dawley,
pubmed-meshheading:21291499-Reperfusion Injury,
pubmed-meshheading:21291499-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:21291499-Up-Regulation
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pubmed:year |
2011
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pubmed:articleTitle |
Epigallocatechin-3-gallate protects kidneys from ischemia reperfusion injury by HO-1 upregulation and inhibition of macrophage infiltration.
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pubmed:affiliation |
Department of Urology, Osaka University Graduate School of Medicine, Osaka, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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