COX-2-derived prostacyclin confers atheroprotection on female mice

Science. 2004 Dec 10;306(5703):1954-7. doi: 10.1126/science.1103333. Epub 2004 Nov 18.

Abstract

Female gender affords relative protection from cardiovascular disease until the menopause. We report that estrogen acts on estrogen receptor subtype alpha to up-regulate the production of atheroprotective prostacyclin, PGI2, by activation of cyclooxygenase 2 (COX-2). This mechanism restrained both oxidant stress and platelet activation that contribute to atherogenesis in female mice. Deletion of the PGI2 receptor removed the atheroprotective effect of estrogen in ovariectomized female mice. This suggests that chronic treatment of patients with selective inhibitors of COX-2 could undermine protection from cardiovascular disease in premenopausal females.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Arteriosclerosis / metabolism
  • Arteriosclerosis / pathology
  • Arteriosclerosis / prevention & control*
  • Cardiovascular Diseases / chemically induced
  • Cells, Cultured
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / adverse effects
  • Cyclooxygenase Inhibitors / pharmacology
  • Epoprostenol / biosynthesis
  • Epoprostenol / metabolism
  • Epoprostenol / physiology*
  • Estradiol / pharmacology
  • Estrogen Receptor alpha / metabolism
  • Female
  • Hydrogen Peroxide / pharmacology
  • Isoenzymes / metabolism*
  • Lactones / adverse effects
  • Lactones / pharmacology
  • Lipid Peroxidation
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / metabolism
  • Myocytes, Smooth Muscle / cytology
  • Myocytes, Smooth Muscle / drug effects
  • Myocytes, Smooth Muscle / metabolism
  • Ovariectomy
  • Oxidative Stress
  • Platelet Activation
  • Prostaglandin-Endoperoxide Synthases / metabolism*
  • Receptors, Epoprostenol / genetics
  • Receptors, Epoprostenol / physiology
  • Receptors, LDL / genetics
  • Receptors, LDL / physiology
  • Sex Characteristics
  • Sulfones / adverse effects
  • Sulfones / pharmacology

Substances

  • Antioxidants
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Estrogen Receptor alpha
  • Isoenzymes
  • Lactones
  • Receptors, Epoprostenol
  • Receptors, LDL
  • Sulfones
  • rofecoxib
  • Estradiol
  • Hydrogen Peroxide
  • Epoprostenol
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases