A comparison of two progestins on myocardial ischemia-reperfusion injury in ovariectomized monkeys receiving estrogen therapy

Coron Artery Dis. 2005 Aug;16(5):301-8. doi: 10.1097/00019501-200508000-00007.

Abstract

Objective: It has been reported that the progestin medroxyprogesterone acetate (MPA), but not norethindrone acetate (NETA), inhibits the beneficial vascular effects of post-menopausal estrogen therapy, but their effects on the myocardium are unclear. The goal of this study is to compare the effects of these two progestins on post-ischemic myocardial damage.

Methods: Ovariectomized monkeys were fed an atherogenic diet for 18 months while receiving, or not receiving (control, n=15), the monkey equivalent to a woman's dose of 5 mug ethinyl estradiol with either 1 mg NETA daily (n=15) or 2.5 mg MPA daily (n=15). The left anterior descending coronary artery was occluded for 1 h and then released to allow myocardial reperfusion for 4 h. Infarct size was quantified using the histochemical stain triphenyl-tetrazolium chloride. Regional myocardial blood flow was measured by 15 mum neutron-activated microspheres, blood pressure and heart rates with a pneumatic cuff, stroke volume by echocardiography, coronary output by thermodilution and neutrophil accumulation in the myocardium using myeloperoxidase (MPO) activity.

Results: The infarct size (area of necrosis/area at risk) was similar between the control group (21+/-3%) and the MPA group (29+/-3%) (P<0.05) but significantly less in the NETA group (3+/-2%) than other groups (P<0.05). The hemodynamic myocardial function and regional myocardial blood values were similar among groups before, during and 4 h after reperfusion (all P-values >0.05). Similarly, there were no treatment effects on MPO activity (P>0.05).

Conclusions: NETA, but not MPA, diminished ischemia-reperfusion injury in estrogen-treated post-menopausal females. The mechanism(s) of this difference remains unclear.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Biomarkers / blood
  • Blood Flow Velocity / drug effects
  • Blood Pressure / drug effects
  • Body Weight / drug effects
  • Contraceptive Agents, Female / pharmacology
  • Coronary Circulation / drug effects
  • Disease Models, Animal
  • Drug Interactions
  • Estrogens / therapeutic use*
  • Estrogens, Conjugated (USP) / therapeutic use
  • Ethinyl Estradiol / therapeutic use
  • Female
  • Haplorhini
  • Heart Rate / drug effects
  • Lipids / blood
  • Medroxyprogesterone Acetate / pharmacology
  • Myocardial Reperfusion Injury / drug therapy*
  • Myocardial Reperfusion Injury / metabolism
  • Myocardial Reperfusion Injury / physiopathology
  • Neovascularization, Physiologic / drug effects
  • Norethindrone / analogs & derivatives
  • Norethindrone / pharmacology
  • Norethindrone Acetate
  • Ovariectomy*
  • Peroxidase / drug effects
  • Progestins / pharmacology*
  • Research Design
  • Stroke Volume / drug effects
  • Vascular Resistance / drug effects

Substances

  • Biomarkers
  • Contraceptive Agents, Female
  • Estrogens
  • Estrogens, Conjugated (USP)
  • Lipids
  • Progestins
  • Ethinyl Estradiol
  • Norethindrone Acetate
  • Medroxyprogesterone Acetate
  • Peroxidase
  • Norethindrone