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Does hypercholesterolaemia alter endothelium-dependent relaxation and NO synthase activity in rabbits?
Does hypercholesterolaemia alter endothelium-dependent relaxation and NO synthase activity in rabbits?
Hypercholesterolaemia in rabbits induces a ~2-fold increase in calcium-independent NO synthase activity in the lungs and depresses endothelium-dependent relaxation in the aorta.
Caution against clinical extrapolation; leaves open relevance of inducible NOS upregulation to human atherosclerosis.
Endothelium-dependent and -independent relaxation of aortic ring preparations was assessed and nitric oxide (NO) synthase activity measured in the lung, and cerebellum of cholesterol-fed and normal rabbits. Endothelium-dependent relaxation of acetylcholine and ATP was depressed while that to the calcium ionophore, A23187, was unaltered in the cholesterol-fed group. Relaxation to sodium nitroprusside was however greater in aortae from the cholesterol-fed animals. Neither Ca(2+)-dependent nor Ca(2+)-independent NO synthase activity could be detected in aortae or hearts taken from either group of animals. Activity of both enzymes was unaltered in cerebellae from both groups of animals. Activity of the Ca(2+)-independent enzyme was however significantly greater (ca. 2 fold) in lungs from the cholesterol-fed rabbits though the activity of the Ca(2+)-dependent NO synthase was not significantly altered. This finding may account for the increased production of nitrogen oxides previously observed in this model of hypercholesterolaemia.
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Lang et al. (1993) studied this question.
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