Source:http://linkedlifedata.com/resource/pubmed/id/11078391
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5 Suppl 1
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pubmed:dateCreated |
2001-2-20
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pubmed:abstractText |
Endothelin-1 (ET-1) has been implicated in many chronic renal glomerular diseases. The purpose of this study was to investigate whether the levels of mRNA expression of endothelin-converting enzyme-1 (ECE-1) and endothelin-A- and -B- (ET(A) and ET(B)) receptors are altered during the progression of interstitial fibrosis following ureter ligation. Rats were subjected to left ureter ligation or a sham operation and euthanized 5 days afterward. Kidneys were fixed in Carnoy's fixative, embedded in paraffin, and sectioned for assessment of interstitial fibrosis by staining for collagen III using immunofluorescence techniques. The area occupied by collagen staining was quantified by image analysis. Kidneys from obstructed rats showed a 54% increase in the area occupied by collagen III staining compared to the contralateral kidney, and an 89% increase compared to sham-operated kidneys. The mRNA levels of ECE-1, as well as ET(A)- and ET(B)-receptors in the kidney were analyzed by Northern blots. It was found that the ECE-1 and ET(A)-receptor mRNA levels in kidneys subjected to ureter ligation increased by 92% and 71%, respectively, when compared with those obtained from the contralateral kidneys. In contrast, mRNA levels of ET(B)-receptors were not significantly different between the two groups. These results suggest that ET-1, through interaction with the ET(A)-receptors, may play a role in the progression of interstitial fibrosis following ureter ligation.
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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/Aspartic Acid Endopeptidases,
http://linkedlifedata.com/resource/pubmed/chemical/Collagen,
http://linkedlifedata.com/resource/pubmed/chemical/Metalloendopeptidases,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Endothelin A,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Endothelin,
http://linkedlifedata.com/resource/pubmed/chemical/endothelin-converting enzyme
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0160-2446
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
36
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
S255-9
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:11078391-Animals,
pubmed-meshheading:11078391-Aspartic Acid Endopeptidases,
pubmed-meshheading:11078391-Blotting, Northern,
pubmed-meshheading:11078391-Collagen,
pubmed-meshheading:11078391-Fibrosis,
pubmed-meshheading:11078391-Fluorescent Antibody Technique,
pubmed-meshheading:11078391-Kidney,
pubmed-meshheading:11078391-Male,
pubmed-meshheading:11078391-Metalloendopeptidases,
pubmed-meshheading:11078391-RNA, Messenger,
pubmed-meshheading:11078391-Rats,
pubmed-meshheading:11078391-Rats, Sprague-Dawley,
pubmed-meshheading:11078391-Receptor, Endothelin A,
pubmed-meshheading:11078391-Receptors, Endothelin,
pubmed-meshheading:11078391-Ureteral Obstruction
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pubmed:year |
2000
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pubmed:articleTitle |
Enhanced expression of renal endothelin-converting enzyme-1 and endothelin-A-receptor mRNA in rats with interstitial fibrosis following ureter ligation.
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pubmed:affiliation |
Metabolic and Cardiovascular Diseases, Novartis Institute for Biomedical Research, Summit, NJ, USA. david.feldman@pharma.novartis.com
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pubmed:publicationType |
Journal Article
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