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来自朝鲜槐的紫铆因同时调节雌激素受体和甲状腺受体。

Tectoridin from Maackia amurensis modulates both estrogen and thyroid receptors.

作者信息

Shim Myeongkuk, Bae Ji-Yeong, Lee Young Joo, Ahn Mi-Jeong

机构信息

College of Life Science, Institute of Biotechnology, Department of Bioscience and Biotechnology, Sejong University, Seoul 143-747, Republic of Korea.

College of Pharmacy and Research Institute of Pharmaceutical Sciences, Gyeongsang National University, Jinju 660-701, Republic of Korea.

出版信息

Phytomedicine. 2014 Apr 15;21(5):602-6. doi: 10.1016/j.phymed.2013.10.022. Epub 2013 Nov 16.

Abstract

AIM

The stem bark of Maackia amurensis has been used as folk medicine for the treatment of cancer, cholecystitis, arthritis, and hyperthyroidism in females. In this study we examined the effects of the ethyl acetate fraction obtained from the 70% ethanol extract of M. amurensis and tectoridin, an active constituent isolated from the ethyl acetate fraction on thyroid and estrogen hormone activity.

METHODS

The effect of the ethanolic extract of M. amurensis stem bark on thyroid hormone activity was evaluated using thyroid hormone responsive-luciferase assay. We isolated tectoridin from the ethyl acetate fraction using a recrystallization method. T-screen assays were used to confirm thyroid hormone activity. The estrogenic activity of the ethyl acetate fraction of M. amurensis and tectoridin was evaluated by estrogen responsive-luciferase assay and estrogen receptor alpha regulation as compared to 17β-estradiol.

RESULTS

Both the ethyl acetate fraction and tectoridin activated thyroid-responsive reporters and increased thyroid hormone-dependent proliferation of rat pituitary GH3 cells, indicating modulation of thyroid hormone receptors. In parallel, the estrogenic activity of the fraction and tectoridin were characterized in a transient transfection system using estrogen-responsive luciferase plasmids in MCF-7 cells. The ethyl acetate fraction and tectoridin activated reporter gene expression and decreased the estrogen receptor protein level.

CONCLUSIONS

These data indicate that tectoridin acts as a weak phytoestrogen as well as a thyroid hormone-like agent by activating both estrogen and thyroid hormone receptors.

摘要

目的

山槐茎皮在民间医学中被用于治疗癌症、胆囊炎、关节炎和女性甲状腺功能亢进。在本研究中,我们检测了从山槐70%乙醇提取物中获得的乙酸乙酯部位以及从该乙酸乙酯部位分离出的活性成分鸢尾苷对甲状腺和雌激素活性的影响。

方法

采用甲状腺激素反应性荧光素酶测定法评估山槐茎皮乙醇提取物对甲状腺激素活性的影响。我们采用重结晶法从乙酸乙酯部位分离出鸢尾苷。采用T-筛选试验确认甲状腺激素活性。与17β-雌二醇相比,通过雌激素反应性荧光素酶测定法和雌激素受体α调节评估山槐乙酸乙酯部位和鸢尾苷的雌激素活性。

结果

乙酸乙酯部位和鸢尾苷均激活甲状腺反应性报告基因,并增加大鼠垂体GH3细胞甲状腺激素依赖性增殖,表明对甲状腺激素受体有调节作用。同时,在MCF-7细胞中使用雌激素反应性荧光素酶质粒的瞬时转染系统中对该部位和鸢尾苷的雌激素活性进行了表征。乙酸乙酯部位和鸢尾苷激活报告基因表达并降低雌激素受体蛋白水平。

结论

这些数据表明,鸢尾苷通过激活雌激素和甲状腺激素受体,既作为一种弱植物雌激素,又作为一种甲状腺激素样物质发挥作用。

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