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Research Article Free access | 10.1172/JCI117971
A. I. Virtanen Institute, University of Kuopio, Finland.
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A. I. Virtanen Institute, University of Kuopio, Finland.
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A. I. Virtanen Institute, University of Kuopio, Finland.
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A. I. Virtanen Institute, University of Kuopio, Finland.
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A. I. Virtanen Institute, University of Kuopio, Finland.
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A. I. Virtanen Institute, University of Kuopio, Finland.
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Published June 1, 1995 - More info
Oxidized low density lipoprotein (LDL) possesses several atherogenic properties. The mechanisms by which LDL becomes oxidized in vivo remain unknown, but previous studies have suggested that 15-lipoxygenase may be one of the factors involved in the initiation of LDL oxidation in the arterial wall. 3 wk after a retrovirus-mediated 15-lipoxygenase gene transfer into iliac arteries of normocholesterolemic rabbits there was a threefold increase in 15-lipoxygenase activity but no signs of LDL oxidation. However, when animals were made moderately hypercholesterolemic by feeding a 0.13% cholesterol diet for 2-3 wk starting from day 4 after the gene transfer, oxidation-specific lipid-protein adducts characteristic of oxidized LDL were detected in 15-lipoxygenase-transduced arteries. Control experiments in which contralateral iliac arteries were transduced with beta-galactosidase-containing retroviruses showed only occasional signs of the presence of oxidation-specific adducts. The results support the hypothesis that products derived from the 15-lipoxygenase activity are involved in the induction of LDL oxidation within the arterial wall, provided that sufficient concentrations of lipoproteins are present in the artery.
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