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白藜芦醇与子宫内膜:利用体内和体外模型深入研究红酒中的一种活性成分

Resveratrol and endometrium: a closer look at an active ingredient of red wine using in vivo and in vitro models.

作者信息

Amaya S C, Savaris R F, Filipovic C J, Wise J D, Hestermann E, Young S L, Lessey B A

机构信息

Department of Obstetrics and Gynecology, Greenville Health System, Greenville, SC, USA.

Departmento de Ginecologia e Obstetrícia, Universidade Federal do Rio Grande do Sul, Brazil Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, NC, USA.

出版信息

Reprod Sci. 2014 Nov;21(11):1362-9. doi: 10.1177/1933719114525271. Epub 2014 Mar 6.

Abstract

Resveratrol is a natural phytoestrogen with antiproliferative properties present in red wine, grapes, and berries. Published reports on the effects of resveratrol in human endometrial function are limited. The objective of this study was to investigate the expression of estrogen receptor α (ESR1), Ki-67 (a proliferative marker), aryl hydrocarbon receptor (AhR), and members of the cytochrome P450 superfamily of enzymes (CYP1A1 and CYP1B1) in an in vitro and vivo assay. Alkaline phosphatase assay of estrogenicity was used to compare estrogen activity of different concentrations of resveratrol to estradiol (E2) and diethylstilbestrol (DES), using Ishikawa cell culture. Immunohistochemical expression of ESR1 and Ki67, and reverse transcriptase polymerase chain reaction of AhR, CYP1A1, and CYP1B1 were analyzed from xenograft implants of human endometrial tissue in ovariectomized immunodeficient RAG-2-γ(c) mice, after 30 days of treatment with subcutaneous pellets of E2, E2 plus progesterone (P4), or E2 plus resveratrol (6, 30, or 60 mg) for 30 days. Compared to E2, resveratrol acted as an agonist and antagonist of estrogen in low and high concentrations, respectively, when combined with E2. Xenografts of human endometrial tissues in RAG-2 mice exhibited reduced expression of ESR1 and proliferative activity (Ki67) with 60 mg of resveratrol. This study suggests that resveratrol, at high doses, has the potential benefit to reduce proliferation of human endometrium through ESR1.

摘要

白藜芦醇是一种天然植物雌激素,具有抗增殖特性,存在于红酒、葡萄和浆果中。关于白藜芦醇对人体子宫内膜功能影响的已发表报告有限。本研究的目的是在体外和体内试验中研究雌激素受体α(ESR1)、Ki-67(一种增殖标志物)、芳烃受体(AhR)以及细胞色素P450酶超家族成员(CYP1A1和CYP1B1)的表达。使用Ishikawa细胞培养,通过碱性磷酸酶雌激素活性测定法比较不同浓度白藜芦醇与雌二醇(E2)和己烯雌酚(DES)的雌激素活性。在用E2、E2加孕酮(P4)或E2加白藜芦醇(6、30或60毫克)皮下植入丸剂处理30天后,从去卵巢免疫缺陷RAG-2-γ(c)小鼠的人子宫内膜组织异种移植植入物中分析ESR1和Ki67的免疫组化表达以及AhR、CYP1A1和CYP1B1的逆转录聚合酶链反应。与E2相比,白藜芦醇与E2联合使用时,在低浓度和高浓度下分别作为雌激素的激动剂和拮抗剂。在RAG-2小鼠中,人子宫内膜组织异种移植物在使用60毫克白藜芦醇时表现出ESR1表达降低和增殖活性(Ki67)降低。本研究表明,高剂量的白藜芦醇有可能通过ESR1减少人子宫内膜的增殖。

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