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首页> 外文期刊>Chemical research in toxicology >Differential Effects of Glycyrrhiza Species on Genotoxic Estrogen Metabolism: Licochalcone A Downregulates P450 1B1, whereas Isoliquiritigenin Stimulates It
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Differential Effects of Glycyrrhiza Species on Genotoxic Estrogen Metabolism: Licochalcone A Downregulates P450 1B1, whereas Isoliquiritigenin Stimulates It

机译:甘草种类对遗传毒性雌激素代谢的不同影响:利考查酮A下调P450 1B1,而异黄体生成素则刺激它。

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摘要

Estrogen chemical carcinogenesis involves 4-hydroxylation of estrone/estradiol (E-1/E-2) by P450 1B1, generating catechol and quinone genotoxic metabolites that cause DNA mutations and initiate/promote breast cancer. Inflammation enhances this effect by upreguIating P450 1B1. The present study tested the three authenticated medicinal species of licorice [Glycyrrhiza glabra (GG), G. uralensis (GU), and G. inflata (GI)] used by women as dietary supplements for their anti-inflammatory activities and their ability to modulate estrogen metabolism. The pure compounds, liquiritigenin (LigF), its chalcone isomer isoliquiritigenin (LigC), and the GI-specific licochalcone A (LicA) were also tested. The licorice extracts and compounds were evaluated for anti-inflammatory activity by measuring inhibition of iNOS activity in macrophage cells: GI GG > GU and LigC congruent to LicA LigF. The Michael acceptor chalcone, LicA, is likely responsible for the anti-inflammatory activity of GI. A sensitive LC-MS/MS assay was employed to quantify estrogen metabolism by measuring 2-MeOE1 as nontoxic and 4-MeOE1 as genotoxic biomarkers in the nontumorigenic human mammary epithelial cell line, MCF-10A. GG, GU, and LigC increased 4-MeOE1, whereas GI and LicA inhibited 2- and 4-MeOE1 levels. GG, GU (5 mu g/mL), and LigC (1 mu M) also enhanced P450 1B1 expression and activities, which was further increased by inflammatory cytokines (TNF-alpha and IFN-gamma). LicA (1, 10 mu M) decreased cytokine- and TCDD-induced P450 1B1 gene expression and TCDD-induced xenobiotic response element luciferase reporter (IC50 = 12.3 mu M), suggesting an antagonistic effect on the aryl hydrocarbon receptor, which regulates P450 1B1. Similarly, GI (5 mu g/mL) reduced cytokine- and TCDD-induced P450 1B1 gene expression. Collectively, these data suggest that, of the three licorice species that are used in botanical supplements, GI represents the most promising chemopreventive licorice extract for women's health. Additionally, the differential effects of the Glycyrrhiza species on estrogen metabolism emphasize the importance of standardization of botanical supplements to species-specific bioactive compounds.
机译:雌激素化学致癌作用涉及通过P450 1B1对雌酮/雌二醇(E-1 / E-2)进行4-羟基化作用,产生导致DNA突变并引发/促进乳腺癌的儿茶酚和醌遗传毒性代谢物。炎症通过调节P450 1B1来增强此效果。本研究测试了三种经认证的甘草药用种[甘草,甘草和甘草],它们被妇女用作膳食补充剂,具有抗炎活性和调节功能雌激素代谢。还测试了纯化合物,liquiritigenin(LigF),其查耳酮异构体异oliquiritigeninin(LigC)和GI特异licochalcone A(LicA)。通过测量对巨噬细胞iNOS活性的抑制作用来评估甘草提取物和化合物的抗炎活性:GI GG> GU和与LicA LigF一致的LigC。迈克尔受体查尔酮LicA可能是胃肠道的抗炎活性。通过在非致瘤性人类乳腺上皮细胞系MCF-10A中通过测量2-MeOE1无毒和4-MeOE1作为遗传毒性生物标记物,采用灵敏的LC-MS / MS分析定量雌激素代谢。 GG,GU和LigC增加4-MeOE1,而GI和LicA抑制2-和4-MeOE1水平。 GG,GU(5μg / mL)和LigC(1μM)也增强了P450 1B1的表达和活性,炎性细胞因子(TNF-α和IFN-γ)进一步增强了P450 1B1的表达和活性。 LicA(1,10μM)降低了细胞因子和TCDD诱导的P450 1B1基因表达,并降低了TCDD诱导的异源响应元件荧光素酶报道分子(IC50 = 12.3μM),表明对调节P450 1B1的芳烃受体具有拮抗作用。 。同样,GI(5μg / mL)降低了细胞因子和TCDD诱导的P450 1B1基因表达。总的来说,这些数据表明,在植物补品中使用的三种甘草中,GI代表了对妇女健康最有前途的化学预防性甘草提取物。另外,甘草种对雌激素代谢的不同作用强调了植物补品标准化为种特异性生物活性化合物的重要性。

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