膳食植物雌激素对人子宫内膜基质细胞芳香化酶活性的影响。

Katie M Edmunds, Alison C Holloway, Denis J Crankshaw, Sanjay K Agarwal, Warren G Foster
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引用次数: 53

摘要

据报道,膳食植物雌激素可抑制胎盘微粒体中的芳香化酶活性,但对人类子宫内膜的影响尚不清楚。芳香化酶是雄激素转化为雌激素的限速酶,最近已被证明在子宫内膜异位症女性的子宫内膜中表达,并被认为在该疾病的病理生理学中发挥作用。因此,本研究的目的是筛选膳食植物雌激素抑制人子宫内膜基质细胞(ESC)芳香化酶活性的能力,并确定治疗子宫内膜异位症的潜在新药物。通过与膳食植物雌激素染料木素、大豆苷元、菊花素和柚皮素的直接相互作用,在无细胞试验中测试了芳香酶活性的抑制。此外,还研究了对ESC培养中芳香酶活性的复合效应。染料木素和大豆苷元对重组人芳香酶活性无抑制作用,而柚皮素和菊花素对重组人芳香酶活性有抑制作用。然而,染料木素(1 nM至1 mM)刺激ESC的芳香酶活性,而其他植物雌激素没有影响。免疫阳性的芳香酶细胞在染料木黄酮处理的ESC中被证实,但在未处理的对照培养中没有。综上所述,我们的数据表明染料木素可能通过增加酶表达来增加ESC的芳香酶活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effects of dietary phytoestrogens on aromatase activity in human endometrial stromal cells.

Dietary phytoestrogens have been reported to inhibit aromatase activity in placental microsomes, but the effects in the human endometrium are unknown. Aromatase, the rate-limiting enzyme in the conversion of androgens to estrogens, has recently been shown to be expressed in the endometrium of women with endometriosis and is thought to play a role in the pathophysiology of this disease. Therefore, the objective of this study was to screen dietary phytoestrogens for their ability to inhibit aromatase activity in human endometrial stromal cells (ESC) and identify potential novel therapeutic agents for the treatment of endometriosis. The inhibition of aromatase activity by direct interaction with the dietary phytoestrogens genistein, daidzein, chrysin, and naringenin was tested in a cell free assay. Furthermore, test compound effects on aromatase activity in ESC cultures were also examined. Genistein and daidzein were inactive in the human recombinant aromatase assay whereas naringenin and chrysin inhibited aromatase activity. However, genistein (1 nM to 1 mM) stimulated aromatase activity in ESC whereas other phytoestrogens had no effect. Immunopositive aromatase cells were demonstrated in genistein-treated ESC but not in untreated control cultures. Taken together, our data suggest that genistein can increase aromatase activity in ESC likely via increased enzyme expression.

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