RENOPROTECTIVE EFFECT OF CONTEMPORARY BLOCKING OF ANGIOTENSIN-II AND ENDOTHELIN-1 IN RATS WITH MEMBRANOUS NEPHROPATHY

Background. We previously showed that chronic administration of an ang iotensin converting enzyme (ACE) inhibitor to rats with passive Heyman n nephritis (PHN), a model of membranous nephropathy with proteinuria and increased renal synthesis of endothelin-l (ET-1), reduces urinary proteins and partially limits the exaggerated ET-1 renal synthesis. He re we compared the effect of an ET, receptor antagonist and an ACE-inh ibitor given as single therapies with a combination of the two drugs i n uninephrectomized PHN rats. Methods. PHN was induced with a single i .v. injection of rabbit anti-Fx1A antibody in 40 male Sprague Dawley r ats. To accelerate the onset of renal damage rats underwent uninephrec tomy seven days later and were subsequently treated until eight months with the ET, receptor antagonist LU-135252 (50 mg/kg b.i.d. p.o.) or the ACE-inhibitor trandolapril (1 mg/kg in the drinking water) or the combination of the two drugs. Results. Either LU-135252 or trandolapri l given alone prevented the increase in systolic blood pressure (SBP). Combined therapy was even more effective than single drugs. While LU1 35252 and trandolapril reduced proteinuria by 23 to 25%, the drug comb ination resulted in 45% lowering of urinary proteins. Serum creatinine was significantly decreased by the combination, but not by the single drugs. Glomerulosclerosis and tubulointerstitial damage were more red uced by combined therapy than by LU-135252 or trandolapril alone. Conc lusions. These data suggest that contemporary blocking angiotensin II (Ang II) and ET-1 in an accelerated model of PHN had an additive renop rotective effect than single blocking Ang II or ET-1 and would represe nt a therapeutic advantage for renal disease patients who do not compl etely respond to ACE inhibitors.