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Article type: Research Article
Authors: Owen, Alice J.; ; | Abbey, Mavis
Affiliations: Department of Physiology, University of Adelaide, Australia | CSIRO Health Sciences and Nutrition, Adelaide, Australia | Smart Foods Centre, University of Wollongong, Australia
Abstract: The present study examined the effect of estrogens and compounds with estrogenic activity on the uptake of atherogenic lipoproteins into macrophages, thought to be the initiating step in the development of atherosclerotic lesions. Isolated low density lipoprotein (LDL) and lipoprotein(a) (Lp(a)) were radiolabelled with ^{3}H-cholesterol linoleate, and incubated with J774 macrophages for 24 hours in the presence of pharmacological doses of estrogens and phytoestrogens. At a concentration of 0.1 μM, the estrogen 17β-estradiol significantly reduced LDL uptake by macrophages by 14% (p < 0.05), but estrone did not have any effect. At 10 μM, both estrogens significantly reduced macrophage LDL uptake, but the phytoestrogenic-lignans enterodiol and enterolactone had no effect on LDL uptake. Lp(a) uptake into cells was significantly reduced by both estrone and estradiol, and by enterolactone and enterodiol at concentrations of 10 μM (p < 0.01), with enterodiol being most effective. The results of this study suggest that the uptake of these structurally similar lipoproteins is regulated differently. Macrophage Lp(a) uptake appears more phytoestrogen sensitive than does LDL uptake.
Keywords: LDL, Lp(a), macrophage, estrogens, phytoestrogens
Journal: BioFactors, vol. 20, no. 3, pp. 119-127, 2004
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