Azilsartan decreases renal and cardiovascular injury in the spontaneously hypertensive obese rat

Cardiovasc Drugs Ther. 2014 Aug;28(4):313-22. doi: 10.1007/s10557-014-6530-0.

Abstract

Purpose: Angiotensin II type 1 receptor blockers (ARBs) are widely used in treating hypertension. In the present study, we tested the hypothesis that a novel ARB, azilsartan medoxomil (AZL-M) will prevent renal and cardiovascular injury in the spontaneously hypertensive obese rat (SHROB), a model of cardiometabolic syndrome.

Methods: Male SHROB were treated with vehicle or AZL-M orally for 56 days. Vehicle treated normotensive Wistar-Kyoto (WKY) rats served as controls. The effects of AZL-M on kidney injury, vascular endothelial and heart functions, lipid profile, and glucose tolerance were assessed.

Results: AZL-M demonstrated anti-hypertensive effects along with markedly improved vascular endothelial function in SHROB. In these rats, AZL-M demonstrates strong kidney protective effects with lower albuminuria and nephrinuria along with reduced tubular cast formation and glomerular injury. AZL-M treatment also improved left ventricular heart function, attenuated development of left ventricular hypertrophy, and reduced cardiac fibrosis in SHROB.

Conclusion: Overall, these findings demonstrate kidney and heart protective effects of AZL-M in SHROB, and these effects were associated with its ability to lower blood pressure and improve endothelial function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antihypertensive Agents / pharmacology
  • Antihypertensive Agents / therapeutic use*
  • Benzimidazoles / pharmacology
  • Benzimidazoles / therapeutic use*
  • Blood Glucose / analysis
  • Body Weight / drug effects
  • Cholesterol / blood
  • Disease Models, Animal
  • Heart / drug effects
  • Hypertension / blood
  • Hypertension / drug therapy*
  • Hypertension / pathology
  • Hypertrophy, Left Ventricular / blood
  • Hypertrophy, Left Ventricular / drug therapy
  • Hypertrophy, Left Ventricular / pathology
  • In Vitro Techniques
  • Insulin / blood
  • Kidney / drug effects
  • Kidney / pathology
  • Male
  • Mesenteric Arteries / drug effects
  • Mesenteric Arteries / physiology
  • Myocardium / pathology
  • Obesity / blood
  • Obesity / drug therapy*
  • Obesity / pathology
  • Oxadiazoles / pharmacology
  • Oxadiazoles / therapeutic use*
  • Protective Agents / pharmacology
  • Protective Agents / therapeutic use*
  • Rats, Inbred WKY
  • Triglycerides / blood
  • Vasodilation / drug effects

Substances

  • Antihypertensive Agents
  • Benzimidazoles
  • Blood Glucose
  • Insulin
  • Oxadiazoles
  • Protective Agents
  • Triglycerides
  • Cholesterol
  • azilsartan medoxomil