“…Nevertheless, the combined treatment displayed marked additional beneficial actions on albuminuria and important renoprotective effects, such as alleviation of the renal glomerular and cortical tubulointerstitial injury. Increased albuminuria is a strong and independent predictor for all-cause mortality in CKD as well as in CHF [3][4][5]7,8,53,55], hence with the prolonged treatment the additive beneficial actions on the course of CKD-and CHF-related mortality could occur. Such reasoning is supported by the favourable actions on renal glomerular and tubulointerstitial morphology: 5/6 + ACF HanSD rats treated within the late treatment protocol with either ET A antagonist alone or ACEi alone showed marked renal glomerular damage, similar as observed in untreated animals.…”