Inhibition of soluble epoxide hydrolase improves the impaired pressure-natriuresis relationship and attenuates the development of hypertension and hypertension-associated end-organ damage in Cyp1a1-Ren-2 transgenic rats

J Hypertens. 2011 Aug;29(8):1590-601. doi: 10.1097/HJH.0b013e328349062f.

Abstract

Objective: In the present study, we compared the effects of treatment with the novel soluble epoxide hydrolase (sEH) inhibitor (c-AUCB) with those of the AT1 receptor antagonist losartan on blood pressure (BP), autoregulation of renal blood flow (RBF) and on glomerular filtration rate (GFR) and the pressure-natriuresis relationship in response to stepwise reduction in renal arterial pressure (RAP) in Cyp1a1-Ren-2 transgenic rats.

Methods: Hypertension was induced in Cyp1a1-Ren-2 rats through dietary administration for 11 days of the natural xenobiotic indole-3-carbinol (I3C) which activates the renin gene. Treatment with c-AUCB and losartan was started 48 h before initiating administration of the diet containing I3C. Rats were prepared for renal functional studies to evaluate in-vivo renal autoregulatory efficiency when RAP was gradually decreased by an aortic clamp.

Results: I3C administration resulted in the development of severe hypertension which was associated with markedly lower basal RBF and GFR and substantially impaired autoregulatory efficiency as well as a suppression of the pressure-natriuresis relationship when compared with noninduced rats. Treatment with c-AUCB significantly decreased BP, improved autoregulatory efficiency of RBF and GFR and the slope of pressure-natriuresis relationship. Treatment with losartan completely prevented the impaired autoregulation and pressure-natriuresis relationship as well as the development of hypertension in I3C-induced rats.

Conclusion: Our present findings indicate that chronic treatment with the sEH inhibitor c-AUCB substantially attenuates the development of malignant hypertension in I3C-induced rats likely via improvement of the renal autoregulatory efficiency and the pressure-natriuresis relationship.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin II Type 1 Receptor Blockers / pharmacology
  • Animals
  • Blood Pressure / drug effects*
  • Blood Pressure / physiology
  • Cytochrome P-450 CYP1A1 / genetics*
  • Disease Models, Animal
  • Enzyme Inhibitors / pharmacology*
  • Epoxide Hydrolases / antagonists & inhibitors*
  • Glomerular Filtration Rate / drug effects
  • Glomerular Filtration Rate / physiology
  • Hypertension, Malignant / chemically induced
  • Hypertension, Malignant / physiopathology
  • Hypertension, Malignant / prevention & control*
  • Indoles / adverse effects
  • Kidney / blood supply
  • Kidney / pathology
  • Kidney / physiopathology
  • Kidney Diseases / physiopathology
  • Kidney Diseases / prevention & control*
  • Losartan / pharmacology
  • Natriuresis / drug effects*
  • Natriuresis / physiology
  • Rats
  • Rats, Transgenic
  • Regional Blood Flow / drug effects
  • Regional Blood Flow / physiology
  • Renin / genetics*

Substances

  • Angiotensin II Type 1 Receptor Blockers
  • Enzyme Inhibitors
  • Indoles
  • Ren2 protein, rat
  • indole-3-carbinol
  • Cytochrome P-450 CYP1A1
  • Epoxide Hydrolases
  • Renin
  • Losartan