4.6 Article

Acute dilatation to phytoestrogens and estrogen receptor subtypes expression in small arteries from women with coronary heart disease

期刊

ATHEROSCLEROSIS
卷 196, 期 1, 页码 49-58

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ELSEVIER IRELAND LTD
DOI: 10.1016/j.atherosclerosis.2007.01.038

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menopause; coronary heart disease (CHD); estrogen receptor; phytoestrogens; arteries

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We tested if endothelial function and estrogen receptor (ER) expression differs between resistance arteries in subcutaneous circulation from postmenopausal women with coronary heart disease (CHID, congruent to 1 year after myocardial infarction, n = 12) and aged matched controls (n = 14); and if acute effects of phytoestrogens (genistein, resveratrol) could be of relevance for vascular protection. We utilized ex vivo small artery (congruent to 350 mu m) bioassays and found no difference in bradykinin (BK)-mediated dilatation between the groups. One-hour incubation with phytoestrogens (natural ER beta agonists), propyl-pyrazole-triol-trisphenol (PPT-selective ER alpha agonist) and 17 beta-estradiol (17 beta-E-2-ER alpha/beta agonist) at 0.01 mu M/L had no effect on BK-induced responses. Concentration-response curves (0.01-30 mu M/L) to investigated compounds were also obtained and compared in separate arteries. We found that dilatation to phytoestrogens was enhanced in CHD if compared to controls (p<0.05), while responses to 17 beta-E-2 remained similar. The dilatation to phytoestrogens was also higher if compared to 17 beta-E-2 (p<0.05) in CHID. In controls, only responses to PPT, but not to phytoestrogens, were enhanced in comparison to 17 beta-E-2 (p<0.05). Inhibition of NO synthase had no effect on dilatation induced by increasing concentrations of investigated compounds. ERP expression was enhanced in the vascular wall from CHD women, while ER alpha predominated in the controls (p<0.05). We suggest that diet supplementation by phytoestrogens may provide cardiovascular benefit for postmenopausal women with CHD. The selective targeting of one of the ER subtype may have implications for women's cardiovascular health. (C) 2007 Elsevier Ireland Ltd. All rights reserved.

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