The soyabean isoflavone genistein modulates endothelial cell behaviour
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چکیده
منابع مشابه
Isoflavone genistein protected high glucose-induced human aortic endothelial cell apoptosis through estrogen receptor-mediated pathway
Objective The aim of this study was to determine if isoflavone genistien had protective effects against high glucose-induced cell apoptosis in human aortic endlthelial cells, and investigate the possible mechanism for this protection. Methods Human aortic endothelial cells subjected to normal (5mM) or high glucose (25mM) were treated with genistein at 0, 50, 100nM. Parallel experiments were per...
متن کاملThe soy isoflavone genistein decreases adipose deposition in mice.
Adipose tissue is responsive to estrogen and expresses both estrogen receptor alpha and beta. To test the hypothesis that the estrogenic soy isoflavone genistein can have effects on adipose tissue, juvenile or adult C57/BL6 mice were ovariectomized and given daily injections of vehicle, 17beta-estradiol (5 microg/kg.d) or genistein (8-200 mg/kg.d) sc for 21-28 d. To test effects of dietary geni...
متن کاملMolecular action of isoflavone genistein in the human epithelial cell line HaCaT
Due to its strong proliferation-reducing effects on keratinocytes, and also anti-inflammatory properties, the isoflavone genistein has already been proposed as a possible antipsoriatic compound. As there is still no detailed information on this topic, we examined the effects of genistein by using an in vitro model of both, normal and "psoriasis-like" keratinocytes at this stage of our work exha...
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BACKGROUND CD39 is the dominant vascular nucleoside triphosphate diphosphohydrolase (NTPDase) that exerts major effects on platelet reactivity by the regulated hydrolysis of extracellular adenine nucleotides. The effects of NTPDases on endothelial cell (EC) activation and apoptosis remain unexplored. MATERIAL AND METHODS Recombinant replication-deficient adenoviruses were constructed with hum...
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ژورنال
عنوان ژورنال: British Journal of Nutrition
سال: 2010
ISSN: 0007-1145,1475-2662
DOI: 10.1017/s0007114510000413