Atherosclerosis Impairs Endothelium-Dependent Vascular Relaxation to Acetylcholine and Thrombin in Primates

Freiman, Paul C.
Mitchell, Gordon G.
Heistad, Donald D.
Armstrong, Mark L.
Harrison, David G.

Cardiovascular Center and Department of Internal Medicine, University of Iowa College of Medicine, Iowa City, Iowa

Address for reprints David G. Harrison, MD, Cardiovascular Division, Department of Internal Medicine, University of Iowa Hospitals, Iowa City, lowa 52242

This manuscript from the University of Iowa was sent to Robert M Berne, Consulting Editor, for review by expert referees, for editorial decision, and final disposition

We gratefully acknowledge the technical assistance of Kristen Orgren, Tony Abboud, and Nancy Gagnon The authors also thank Marlene Blakley for secretarial assistance.

Published as an abstract in Fed Proc. 44:523, 1985

Dr. Freiman is a recipient of NHLB1 NRSA (HL07176) Dr Harrison is a recipient of an NHLBI Clinical Investigator Award (HL01046) Supported by American Heart Association Grant-in-Atd 831069, NIH Grants HL27633, HL20827, and HL 14388, lschemic SCOR HL32295, and Atherosclerosis SCOR HL 14230

Received October 30, 1985, accepted for publication February 14, 1986

Circulation Research 58(6):p 783-789, June 1986.

SUMMARY

To test the hypothesis that atherosclerosis impairs endothelium-dependent vascular relaxation, we examined the effect of the endothelium-dependent vasodilators acetylcholine and thrombin and the endothelium-independent vasodilator nitroglycerin on iliac arteries from normal cynomolgus monkeys and cynomolgus monkeys with diet-induced atherosclerosis. Rings of iliac artery were suspended in organ chambers at their optimal length for generating tension. After preconstriction with prostaglandin F2, cumulative concentration-response curves to acetylcholine, thrombin, and nitroglycerin were examined The presence of endothehum was confirmed in each vessel by scanning electron microscopy. Atherosclerotic vessels showed morpholigic evidence of moderate to severe atherosclerosis. Acetylcholine produced a maximal relaxation of 65 ± 10% in the normal group and 27 ± 10% in atherosclerotic vessels (P < 0 05). Thrombin (10 0 U/ml) produced relaxation of 39 ± 9% in the normal group and 13 ± 7% in atherosclerotic iliac arteries (P < 0.05). Nitroglycerin relaxed both normal and atherosclerotic blood vessels to an equal extentmaximal relaxation was 92 ± 4% in normal vessels and 98 ± 2% in atherosclerotic vessels To determine if hypercholesterolemia alone produces an abnormality in endothelium-dependent relaxation, we performed two additional studies First, because veins are exposed to hypercholesterolemia, but do not develop atherosclerosis, we studied relaxation responses to acetylcholine and thrombin in veins from normal monkeys and monkeys with diet-induced atherosclerosis. Veins from normal and atherosclerotic monkeys relaxed to a similar extent upon exposure to the endothelium-dependent vasodilators acetylcholine and thrombin Second, we studied relaxation responses to acetylcholine, thrombin, and nitroglycerin in left circumflex coronary arteries from normal dogs and dogs fed a hypercholesterolemic diet for 4–5 weeks when serum cholesterol levels were elevated (serum cholesterol 442 ± 14 mg/dl), but before the onset of atherosclerosis. The endothelium-dependent vasodilators acetylcholine and thrombin produced equivalent degrees of relaxation in arteries removed from normal and hypercholesterolemic dogs These studies demonstrate that atherosclerosis impairs endothelium-dependent relaxation in primate iliac arteries, and that this impairment is not due to a generalized defect in the endothelium caused by hypercholesterolemia, but requires the presence of atherosclerosis