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
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.