Key result
Both ilepatril and olmesartan conferred strong cardiorenal protection in rats with renal failure, but olmesartan provided better protection against the increase in albuminuria.
Why the study?
Does treatment with ilepatril or olmesartan improve left ventricular function and renal damage in rats with renal failure?
Does treatment with ilepatril or olmesartan improve left ventricular function and renal damage in rats with renal failure?
In a rat model of renal failure, both vasopeptidase inhibition and ARB therapy provided comparable cardioprotection, but the ARB offered superior protection against albuminuria.
Answers are grounded in this paper and cite their sources.
Rat model data suggest potential cardiorenal benefits but should not change practice; leaves open translation of olmesartan's albuminuria advantage to humans.
OBJECTIVE: The aim of the present study was to compare the preventive impact of treatment with a vasopeptidase inhibitor (VPI) with an angiotensin-receptor blocker (ARB) on left ventricular (LV) function and renal damage in rats with renal failure after 5/6 renal ablation (Nx). METHODS: Rats (n = 15-20, each group) underwent either sham-operation (Sham) or 5/6 renal ablation (Nx). Two additional groups of Nx-animals (groups Nx-VPI and Nx-ARB) were treated with the VPI ilepatril (AVE7688, 30 mg kg(-1) d(-1)) or with the ARB olmesartan (10 mg kg(-1 )d(-1)). Animals were followed for 4 weeks. RESULTS: Systolic blood pressure (SBP), LV hypertrophy (LVH) and LV end-diastolic pressure (LVEDP) were increased 4 weeks after Nx (p < 0.05). LV pressure rise (+dP/dt/LVPmax), LV pressure fall (-dP/dt/LVPmax), and creatinine clearance decreased, while albuminuria and renal glomerulosclerosis index (GSI) increased with Nx (p < 0.05, respectively). In comparison to Nx, treatment with both VPI and ARB normalized SBP, LVH, LVEDP, +dP/dt/LVPmax, and -dP/dt/LVPmax to Sham control levels. GSI, but not creatinine clearance, was also normalized in response to both treatments. The significant increase in albuminuria observed in Nx (+230-fold versus Sham, p < 0.0001) was partially reduced in Nx-VPI (+47-fold versus Sham, p < 0.0001) and fully abolished in Nx-ARB. CONCLUSIONS: Both ilepatril and olmesartan conferred strong cardiorenal protective effects in rats with renal failure. While cardioprotection was clearly comparable with both treatment regimens, the ARB provided a better protection against the increase in albuminuria, although renal function and structural kidney changes were similarly affected by the VIP and ARB.
No takes yet. Share an insight, caveat, or question.
Halleck et al. (2014) studied Experimental hypertension with renal failure. Ilepatril (vasopeptidase inhibitor) and Olmesartan (angiotensin-receptor blocker) vs. Untreated 5/6 renal ablation (Nx) and Sham-operation was evaluated on Left ventricular function and renal damage (p=<0.05). Both ilepatril and olmesartan conferred strong cardiorenal protection in rats with renal failure, but olmesartan provided better protection against the increase in albuminuria.
Synapse has enriched 10 related papers. Consider them for comparative context: