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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1996-5-14
pubmed:abstractText
Renal disease progression in the rat is associated with a time-dependent upregulation of renal endothelin-1 (ET-1) gene expression and synthesis. We have previously demonstrated that endothelin A receptor subtype (ETA) blockade in rats with remnant kidney reduced signs of disease activity, suggesting that ET-1 exerts part of its deleterious effects on the kidney through ETA. No data are available so far on the role of ETB receptor in progressive renal injury. We first studied renal ETA and ETB receptor gene expression in rats with remnant kidney on days 7, 30, and 120 after the surgical procedure. While renal expression of ETA was unaffected, ETB receptor gene was significantly upregulated with time in rats with remnant kidney, being 3.5-fold and sixfold higher than shamoperated rats at days 30 and 120. We also evaluated whether bosentan, a nonpeptidic ETA and ETB receptor antagonist, offered better protection against renal disease progression than reported for ETA-selective blockers and whether it improved survival in animals with renal ablation. Two groups of rats with renal mass reduction (n = 11 each) were given bosentan 100 mg/kg/d orally or its vehicle (carboxymethyl cellulose) beginning day 7 after the surgical procedure and were followed until the death of the vehicle-treated animals. Sham-operated animals comprised the control group. Bosentan partially prevented increases in blood pressure and proteinuria, but had a remarkable protective effect on renal function and significantly prolonged animal survival. These data suggest that blocking both renal ETA and ETB receptors might have major implications in the treatment of human progressive nephropathies.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0272-6386
pubmed:author
pubmed:issnType
Print
pubmed:volume
27
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
416-23
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed-meshheading:8604712-Analysis of Variance, pubmed-meshheading:8604712-Animals, pubmed-meshheading:8604712-Blotting, Northern, pubmed-meshheading:8604712-Disease Models, Animal, pubmed-meshheading:8604712-Disease Progression, pubmed-meshheading:8604712-Drug Evaluation, Preclinical, pubmed-meshheading:8604712-Gene Expression Regulation, pubmed-meshheading:8604712-Humans, pubmed-meshheading:8604712-Kidney, pubmed-meshheading:8604712-Kidney Diseases, pubmed-meshheading:8604712-Male, pubmed-meshheading:8604712-Nephrectomy, pubmed-meshheading:8604712-Rats, pubmed-meshheading:8604712-Rats, Sprague-Dawley, pubmed-meshheading:8604712-Receptor, Endothelin A, pubmed-meshheading:8604712-Receptor, Endothelin B, pubmed-meshheading:8604712-Receptors, Endothelin, pubmed-meshheading:8604712-Sulfonamides
pubmed:year
1996
pubmed:articleTitle
Blocking both type A and B endothelin receptors in the kidney attenuates renal injury and prolongs survival in rats with remnant kidney.
pubmed:affiliation
Mario Negri Institute for Pharmacological Research, Bergamo, Italy.
pubmed:publicationType
Journal Article