Interactions of Phytoestrogens with Estrogen Receptors α and β(3). Estrogenic Activities of Soy Isoflavone Aglycones and Their Metabolites Isolated from Human Urine
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- Kinjo Junei
- Faculty of Pharmaceutical Sciences, Fukuoka University
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- Tsuchihashi Ryota
- Faculty of Pharmaceutical Sciences, Kumamoto University
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- Morito Keiko
- Faculty of Pharmaceutical Sciences, Kanazawa University
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- Hirose Toshiharu
- Faculty of Pharmaceutical Sciences, Kanazawa University
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- Aomori Tohru
- Faculty of Pharmaceutical Sciences, Kanazawa University
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- Nagao Tsuneatsu
- Faculty of Pharmaceutical Sciences, Fukuoka University
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- Okabe Hikaru
- Faculty of Pharmaceutical Sciences, Fukuoka University
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- Nohara Toshihiro
- Faculty of Pharmaceutical Sciences, Kumamoto University
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- Masamune Yukito
- Faculty of Pharmaceutical Sciences, Kanazawa University
書誌事項
- タイトル別名
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- Interactions of Phytoestrogens with Estrogen Receptors .ALPHA. and .BETA. (III). Estrogenic Activities of Soy Isoflavone Aglycones and Their Metabolites Isolated from Human Urine
- Interactions of Phytoestrogens with Estrogen Receptors アルファ and ベータ 3 Estrogenic Activities of Soy Isoflavone Aglycones and Their Metabolites Isolated from Human Urine
- Interactions of phytoestrogens with estrogen receptors α and β (III). Estrogenic activities of soy isoflavone aglycones and their metabolites isolated from human urine
- Interaction of phytoestrogens with estrogen receptors α and β (III). Estrogenic activities of soy isoflavones and their metabolites isolated from human urine
この論文をさがす
説明
Two glucuronides (4′-O-, and 7-O-) and a glucuronyl (7-O-) sulfate (4′-O-) of genistein, two glucuronides (4′-O-, and 7-O-) and a glucuronyl (7-O-) sulfate (4′-O-) of daidzein, 7-O-glucuronides of glycitein, dihydrodaidzein and O-desmethylangolensin were isolated from the urine of volunteer subjects fed soy bean curds (Tofu). The estrogenic activities, i.e., i) the effect on the estrogen-dependent growth of MCF-7 cells, ii) the binding ability to human estrogen receptors (hERs) α and β, and iii) the effect on hER-dependent β-galactosidase induction, of these isoflavone metabolites were examined. Two synthetic isoflavone aglycones (dihydrodaidzein and O-desmethylangolensin) and four synthetic sulfates (4′-O- and 4′-, 7-di-O-) of genistein and daidzein were also studied for their estrogenic activities for the purpose of comparison. With respect to estrogenic acivity, the tested isoflavone metabolites were classified into three groups. The first group shows a very poor stimulatory effect toward the growth of MCF-7 cells, binding activity, and β-galactosidase induction. The sulfates belong to this group. The second group shows a moderate binding activity but poor stimulation and β-galactosidase induction. Some glucuronyl conjugates belong to this group. The last group shows a moderate stimulation and β-galactosidase induction but poor binding activity. A mixed type of conjugates having glucuronyl and sulfony moieties belong to this group.
収録刊行物
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- Biological & Pharmaceutical Bulletin
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Biological & Pharmaceutical Bulletin 27 (2), 185-188, 2004
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204624957312
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- NII論文ID
- 110003608726
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- NII書誌ID
- AA10885497
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- ISSN
- 13475215
- 09186158
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- NDL書誌ID
- 6827063
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- PubMed
- 14758030
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- JaLC
- NDLサーチ
- Crossref
- PubMed
- CiNii Articles
- OpenAIRE
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- 抄録ライセンスフラグ
- 使用不可