Enhanced coronary vasoconstriction to oxidative stress product, 8-epi-prostaglandinF2 alpha, in experimental hypercholesterolemia

Cardiovasc Res. 1999 Dec;44(3):601-7. doi: 10.1016/s0008-6363(99)00225-4.

Abstract

Objectives: The F2-isoprostanes are a family of novel prostaglandin isomers and a stable product of in vivo oxidative stress. 8-epi-prostaglandinF2 alpha, a member of this isoprostane family, is a vasoconstrictor and its local release may contribute to the abnormal vasomotor tone associated with hypercholesterolemia. We therefore aimed to outline the role of 8-epi-prostaglandinF2 alpha as a coronary vasoconstrictor in experimental hypercholesterolemia.

Methods and results: Pigs were randomized to two experimental groups (each n = 9): normal (N) and high cholesterol (HC) diet. To determine the vasoconstrictive effects of 8-epi-prostaglandinF2 alpha in vitro, doses from 10(-9) to 10(-5) M were used to constrict coronary epicardial rings. Plasma total and LDL cholesterol levels were significantly higher in the HC group compared with the N group (P < 0.005) as were plasma 8-epi-prostaglandinF2 alpha levels (P < 0.001). 8-epi-prostaglandinF2 alpha immunoreactivity was present in the vessel wall in both groups. Normal vessels with intact endothelium (n = 8 rings) contracted to 8-epi-prostaglandinF2 alpha (maximal contraction 15.5 +/- 8.74%). In the HC group, rings with intact endothelium had a greater contractile response to 8-epi-prostaglandinF2 alpha compared to normals (72.3 +/- 7.9%; n = 8; P < 0.0001). This was reversed by preincubation with NOR-3, a NO donor (maximal contraction 6.7 +/- 1.56%; n = 5; P < 0.0001). Enhanced contraction in normal vessels occurred with endothelial denudation (98.4 +/- 3.56%; n = 6; P < 0.0001) and with preincubation of the endothelium-intact rings with L-NMMA (N-monomethyl-L-arginine), an NO synthase inhibitor (85.5 +/- 10.3%, n = 6, P < 0.001). The enhanced contraction seen with hypercholesterolemia did not occur with other prostanoid vasoconstrictors.

Conclusion: Experimental hypercholesterolemia leads to a significant increase in 8-epi-prostaglandinF2 alpha levels in addition to enhanced 8-epi-prostaglandinF2 alpha-induced coronary vasoconstriction, in vitro. These findings support a role for the F2-isoprostanes in the regulation of coronary vasomotor tone in pathophysiologic states.

Publication types

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

MeSH terms

  • 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid / pharmacology
  • Analysis of Variance
  • Animals
  • Arginine / pharmacology
  • Arteries / chemistry
  • Bridged Bicyclo Compounds, Heterocyclic
  • Cholesterol / blood
  • Cholesterol, HDL / blood
  • Cholesterol, LDL / blood
  • Coronary Vessels / drug effects*
  • Dinoprost / analogs & derivatives*
  • Dinoprost / analysis
  • Dinoprost / pharmacology
  • Dinoprostone / analogs & derivatives
  • Dinoprostone / pharmacology
  • Endothelium, Vascular / drug effects
  • Enzyme Inhibitors / pharmacology
  • Fatty Acids, Unsaturated
  • Female
  • Hydrazines / pharmacology
  • Hypercholesterolemia / metabolism*
  • Immunohistochemistry
  • In Vitro Techniques
  • Muscle, Smooth, Vascular / drug effects
  • Nitric Oxide / metabolism
  • Nitric Oxide Donors / pharmacology
  • Nitric Oxide Synthase / antagonists & inhibitors
  • Nitro Compounds / pharmacology
  • Oxidative Stress*
  • Random Allocation
  • Swine
  • Thromboxane A2 / antagonists & inhibitors
  • Vasoconstriction / drug effects*
  • Vasoconstrictor Agents / pharmacology
  • omega-N-Methylarginine / pharmacology

Substances

  • Bridged Bicyclo Compounds, Heterocyclic
  • Cholesterol, HDL
  • Cholesterol, LDL
  • Enzyme Inhibitors
  • Fatty Acids, Unsaturated
  • Hydrazines
  • Nitric Oxide Donors
  • Nitro Compounds
  • Vasoconstrictor Agents
  • 8-epi-prostaglandin F2alpha
  • omega-N-Methylarginine
  • Nitric Oxide
  • Thromboxane A2
  • 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid
  • SQ 29548
  • FK 409
  • Arginine
  • Cholesterol
  • Dinoprost
  • Nitric Oxide Synthase
  • Dinoprostone