Source:http://linkedlifedata.com/resource/pubmed/id/19895808
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-3
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pubmed:dateCreated |
2010-1-27
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pubmed:abstractText |
Advanced glycation end products (AGE) have been implicated in the pathogenesis of diabetic complications. The purpose of this study was to examine the novel coumarin-aspirin compound XLF-III-43 in the inhibition of AGE formation in diabetic nephropathy. In vitro analysis showed XLF-III-43 in a dose-dependent manner decreased glucose induced formation of glycation adducts on albumin and inhibited AGE-lysozyme crosslinking. The streptozotocin-induced diabetic rats were used to investigate the beneficial effects of XLF-III-43 treatment on diabetic nephropathy. Administration of XLF-III-43 significantly decreased (P<0.05) blood urea nitrogen and urinary albumin excretion. Moreover, XLF-III-43 ameliorated kidney hypertrophy, mesangial expansion and glomerulosclerosis in diabetic rats relative to untreated model group. These data correlated with decreased both AGE and downstream markers of AGE stress (TGF-beta1, CTGF, fibronectin and collagen IV fibrolysis) in kidneys of diabetic rats. These data support further development of XLF-III-43 for prevention of nephropathy via inhibition of AGE formation consequent to chronic hyperglycemia.
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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 |
Feb
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pubmed:issn |
1879-0712
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pubmed:author | |
pubmed:copyrightInfo |
Crown Copyright (c) 2009. Published by Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
10
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pubmed:volume |
627
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
340-7
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pubmed:meshHeading |
pubmed-meshheading:19895808-Animals,
pubmed-meshheading:19895808-Body Weight,
pubmed-meshheading:19895808-Coumarins,
pubmed-meshheading:19895808-Diabetes Mellitus, Experimental,
pubmed-meshheading:19895808-Diabetic Nephropathies,
pubmed-meshheading:19895808-Female,
pubmed-meshheading:19895808-Gene Expression Regulation,
pubmed-meshheading:19895808-Glycosylation End Products, Advanced,
pubmed-meshheading:19895808-Hyperglycemia,
pubmed-meshheading:19895808-Hypertension,
pubmed-meshheading:19895808-Kidney,
pubmed-meshheading:19895808-Rats,
pubmed-meshheading:19895808-Rats, Sprague-Dawley,
pubmed-meshheading:19895808-Salicylic Acids
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pubmed:year |
2010
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pubmed:articleTitle |
XLF-III-43, a novel coumarin-aspirin compound, prevents diabetic nephropathy in rats via inhibiting advanced glycation end products.
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pubmed:affiliation |
Department of Pharmacology, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, 1 Xian Nong Tan Street, Beijing 100050, China. lhy2116@gmail.com
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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