Renin-angiotensin system blockade alone or combined with ETA receptor blockade: effects on the course of chronic kidney disease in 5/6 nephrectomized Ren-2 transgenic hypertensive rats

Clin Exp Hypertens. 2017;39(2):183-195. doi: 10.1080/10641963.2016.1235184. Epub 2017 Mar 1.

Abstract

Background: Early addition of endothelin (ET) type A (ETA) receptor blockade to complex renin-angiotensin system (RAS) blockade has previously been shown to provide better renoprotection against progression of chronic kidney disease (CKD) in Ren-2 transgenic hypertensive rats (TGR) after 5/6 renal ablation (5/6 NX). In this study, we examined if additional protection is provided when ETA blockade is applied in rats with already developed CKD.

Methods: For complex RAS inhibition, an angiotensin-converting enzyme inhibitor along with angiotensin II type 1 receptor blocker was used. Alternatively, ETA receptor blocker was added to the RAS blockade. The treatments were initiated 6 weeks after 5/6 NX and the follow-up period was 50 weeks.

Results: When applied in established CKD, addition of ETA receptor blockade to the complex RAS blockade brought no further improvement of the survival rate (30% in both groups); surprisingly, aggravated albuminuria (588 ± 47 vs. 245 ± 38 mg/24 h, p < 0.05) did not reduce renal glomerular injury index (1.25 ± 0.29 vs. 1.44 ± 0.26), did not prevent the decrease in creatinine clearance (203 ± 21 vs. 253 ± 17 µl/min/100 g body weight), and did not attenuate cardiac hypertrophy to a greater extent than observed in 5/6 NX TGR treated with complex RAS blockade alone.

Conclusions: When applied in the advanced phase of CKD, addition of ETA receptor blockade to the complex RAS blockade brings no further beneficial renoprotective effects on the CKD progression in 5/6 NX TGR, in addition to those seen with RAS blockade alone.

Keywords: 5/6 nephrectomy; Chronic kidney disease; endothelin system; hypertension; renin–angiotensin system.

MeSH terms

  • Albuminuria
  • Angiotensin II Type 1 Receptor Blockers / pharmacology*
  • Angiotensin-Converting Enzyme Inhibitors / pharmacology*
  • Angiotensins / drug effects
  • Angiotensins / metabolism
  • Animals
  • Atrasentan
  • Blood Pressure / drug effects*
  • Cardiomegaly
  • Creatinine / metabolism
  • Disease Progression
  • Drug Therapy, Combination
  • Endothelin A Receptor Antagonists / pharmacology*
  • Glomerular Filtration Rate / drug effects*
  • Hypertension
  • Indoles / pharmacology
  • Kidney / drug effects*
  • Kidney / metabolism
  • Losartan / pharmacology
  • Male
  • Nephrectomy
  • Pyrrolidines / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Transgenic
  • Receptor, Endothelin A / drug effects
  • Receptor, Endothelin A / metabolism
  • Receptor, Endothelin B / drug effects
  • Receptor, Endothelin B / metabolism
  • Renal Insufficiency, Chronic / metabolism*
  • Renin / drug effects
  • Renin / metabolism
  • Renin-Angiotensin System / drug effects*
  • Survival Rate

Substances

  • Angiotensin II Type 1 Receptor Blockers
  • Angiotensin-Converting Enzyme Inhibitors
  • Angiotensins
  • Endothelin A Receptor Antagonists
  • Indoles
  • Pyrrolidines
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • trandolapril
  • Creatinine
  • Renin
  • Losartan
  • Atrasentan