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      Impairment of endothelium-dependent arterial relaxation by lysolecithin in modified low-density lipoproteins.

      Nature
      Acetylcholine, pharmacology, Animals, Aorta, drug effects, physiology, Calcimycin, Cells, Cultured, Endothelium, Vascular, In Vitro Techniques, Kinetics, Lipoproteins, LDL, Lysophosphatidylcholines, Muscle, Smooth, Vascular, Nitroglycerin, Oxidation-Reduction, Phenylephrine, Rabbits, Vasodilation

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          Abstract

          Atherosclerosis in animals and humans is associated with an unresponsiveness of arteries and arterioles to endothelium-dependent vasodilators--agents acting on smooth muscle indirectly by stimulating the release from endothelial cells of a vasodilator principle (endothelium-derived relaxing factor). Altered vasomotor regulation in atherosclerosis could partly reflect an injurious action of abnormal lipoproteins on endothelium. Recently, 'cell-modified' or 'oxidized' low-density lipoprotein (EC-LDL) has received increasing attention because of its potential cytotoxic and atherogenic properties. We report here that arteries exposed to EC-LDL in vitro show an endothelium-dependent vasoregulatory impairment closely resembling that of atherosclerotic arteries. Our results indicate that transfer of lysolecithin from EC-LDL to endothelial membranes produces a selective unresponsiveness to receptor-regulated endothelium-dependent vasodilators.

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