Impact of antihypertensive therapy on the skeleton: effects of enalapril and AT1 receptor antagonist losartan in female rats

Physiol Res. 2001;50(4):353-8.

Abstract

No data are available about the effects of AT1 receptor antagonist losartan on the skeleton and there is also little information on the activity of an ACE inhibitor enalapril on bone metabolism. It is widely believed that the vasculature plays an important role in bone remodeling under normal and pathological conditions. We treated 14-week-old female Wistar rats with losartan, enalapril or saline. Administration of the ACE inhibitor enalapril and angiotensin II antagonist losartan had no effect on total malondialdehyde (MDA) in the blood and on urinary excretion of some eicosanoids and their metabolites. The administration of enalapril and losartan in a dose recommended for the treatment of hypertension did not cause significant changes in bone density, the ash and mineral content or morphometric parameters of the femur compared to the values found in control female rats.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 6-Ketoprostaglandin F1 alpha / urine
  • Angiotensin Receptor Antagonists
  • Animals
  • Antihypertensive Agents / pharmacology*
  • Bone Density / drug effects*
  • Dinoprost* / analogs & derivatives*
  • Dinoprostone / urine
  • Enalapril / pharmacology*
  • F2-Isoprostanes / urine
  • Female
  • Femur / drug effects
  • Femur / metabolism
  • Losartan / pharmacology*
  • Proteinuria / metabolism
  • Rats
  • Rats, Wistar
  • Receptor, Angiotensin, Type 1
  • Thromboxane B2 / urine

Substances

  • Angiotensin Receptor Antagonists
  • Antihypertensive Agents
  • F2-Isoprostanes
  • Receptor, Angiotensin, Type 1
  • 8-epi-prostaglandin F2alpha
  • Thromboxane B2
  • 6-Ketoprostaglandin F1 alpha
  • Enalapril
  • Dinoprost
  • Losartan
  • Dinoprostone