AN ORALLY-ACTIVE ET(A) ET(B) RECEPTOR ANTAGONIST AMELIORATES PROTEINURIA AND GLOMERULAR-LESIONS IN RATS WITH PROLIFERATIVE NEPHRITIS/

Citation
D. Gomezgarre et al., AN ORALLY-ACTIVE ET(A) ET(B) RECEPTOR ANTAGONIST AMELIORATES PROTEINURIA AND GLOMERULAR-LESIONS IN RATS WITH PROLIFERATIVE NEPHRITIS/, Kidney international, 50(3), 1996, pp. 962-972
Citations number
44
Categorie Soggetti
Urology & Nephrology
Journal title
ISSN journal
00852538
Volume
50
Issue
3
Year of publication
1996
Pages
962 - 972
Database
ISI
SICI code
0085-2538(1996)50:3<962:AOEERA>2.0.ZU;2-D
Abstract
The proliferation of mesangial cells and the: extracellular matrix exp ansion constitute the most outstanding morphological aspects of thr ma jority of progressive glomerular diseases. In vitro, endothelin-l (ET- I) is mitogenic for mesangial cells and induces matrix protein synthes is. We studied the possible participation of ET-I in the pathogenesis of renal damage in a normotensive model oi proliferative nephritis. Co incidentally with maximal proteinuria and glomerular lesions, an incre ase was found in the glomerular mRNA expression of preproET-1 and the ET(A) receptor (10 and 6 times compared to controls, respectively), bu t not of the ET(B) receptor. and in ET-1 urinary excretion (217 +/- 33 vs. 84 +/- 4 pg ET-1/24 hr, A:= 4 to 5, P < 0.05). By in situ hybridi zation, an increase in preproET-1 mRNA expression in glomerular endoth elial, epithelial and mesangial cells, and in some tubular cells was o bserved. The administration of bosentan, an ET(A)/ET(B) receptor antag onist. had a beneficial effect on tilt: evolution of nephritis. preven ting the appearance of intense proteinuria (76 +/- 35 vs. 380 +/- 77 m g/24 kr, N = 4 to 5, P < 0.05), the morphological lesions and thr rena l function impairment (creatinine clearance 367 +/- 46 vs. 268 +/- 33 mu l/min/100 g, N = 4 to 5). Simultaneously, there was a decrease in E T-1 urinary excretion (88 +/- 14 vs. 217 +/- 33 pgET-1/24 hr, N = 4:5, P < 0.05) and in the renal preproET-1 mRNA expression. The mean systo lic blood pressures remained in the normal range in all animals. These data indicate that ET-I participates in the pathogenesis of proteinur ia and glomerular injury in a modal of proliferative nephritis. The no npeptidic orally active ET(A)/ET(B) receptor antagonists could be usef ul in the treatment of some human nephritis.