The estrogenic activity of certain phytoestrogens in the siberian sturgeon Acipenser baeri
Identifieur interne : 000265 ( France/Analysis ); précédent : 000264; suivant : 000266The estrogenic activity of certain phytoestrogens in the siberian sturgeon Acipenser baeri
Auteurs : C. Pelissero [France] ; B. Bennetau [France] ; P. Babin [France] ; Françoise Le Menn [France] ; J. Dunogues [France]Source :
- Journal of Steroid Biochemistry and Molecular Biology [ 0960-0760 ] ; 1991.
English descriptors
- KwdEn :
- Animals, Chromans (chemistry), Chromatography, Thin Layer, Coumestrol (chemistry), Equol, Estrogens (chemistry), Estrogens (metabolism), Estrogens, Non-Steroidal, Fishes, Gas Chromatography-Mass Spectrometry, Genistein, Isoflavones (chemistry), Liver (metabolism), Magnetic Resonance Spectroscopy, Phytoestrogens, Plant Preparations, Spectrophotometry, Infrared, Vitellogenins (analysis), Vitellogenins (biosynthesis).
- MESH :
- chemical , analysis : Vitellogenins.
- chemical , biosynthesis : Vitellogenins.
- chemical , chemistry : Chromans, Coumestrol, Estrogens, Isoflavones.
- chemical , metabolism : Estrogens.
- metabolism : Liver.
- Animals, Chromatography, Thin Layer, Equol, Estrogens, Non-Steroidal, Fishes, Gas Chromatography-Mass Spectrometry, Genistein, Magnetic Resonance Spectroscopy, Phytoestrogens, Plant Preparations, Spectrophotometry, Infrared.
Abstract
Various phytoestrogens such as formononetin, daidzein, genistein and equol were synthesized. Their purity was assessed by various analytical techniques including melting point determination, thin-layer chromatography (TLC), infra-red spectra (i.r. spectra), nuclear magnetic resonance (1H- and 13C-NMR) and gas chromatography coupled with mass spectrometry (GC-MS). The estrogenic activity of these compounds, as well as biochanin A and coumestrol, was biologically tested by the induction of vitellogenin secretion in yearling sturgeon and compared to the activity of estradiol-17β.Pure daidzein, biochanin A, genistein, equol and coumestrol all had estrogenic activity as assessed by their induction of hepatic synthesis of vitellogenin when administrated intraperitoneally to yearling Siberian sturgeon. Coumestrol seemed to be the most potent compound, inducing the most vitellogenin secretion with the lowest dose administered. Formononetin was inactive when administered by the intraperitoneal route. All the phytoestrogens tested were considerably less potent than estradiol-17β.
Url:
DOI: 10.1016/0960-0760(91)90100-J
Affiliations:
- France
- Aquitaine, Nouvelle-Aquitaine
- Bordeaux, Talence Cédex
- Université Bordeaux I, Université de Bordeaux
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ISTEX:6C0ADB3972C168F988263D23D947AE561FD3935CLe document en format XML
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Their purity was assessed by various analytical techniques including melting point determination, thin-layer chromatography (TLC), infra-red spectra (i.r. spectra), nuclear magnetic resonance (1H- and 13C-NMR) and gas chromatography coupled with mass spectrometry (GC-MS). The estrogenic activity of these compounds, as well as biochanin A and coumestrol, was biologically tested by the induction of vitellogenin secretion in yearling sturgeon and compared to the activity of estradiol-17β.Pure daidzein, biochanin A, genistein, equol and coumestrol all had estrogenic activity as assessed by their induction of hepatic synthesis of vitellogenin when administrated intraperitoneally to yearling Siberian sturgeon. Coumestrol seemed to be the most potent compound, inducing the most vitellogenin secretion with the lowest dose administered. Formononetin was inactive when administered by the intraperitoneal route. All the phytoestrogens tested were considerably less potent than estradiol-17β.</div></front></TEI><affiliations><list><country><li>France</li></country><region><li>Aquitaine</li><li>Nouvelle-Aquitaine</li></region><settlement><li>Bordeaux</li><li>Talence Cédex</li></settlement><orgName><li>Université Bordeaux I</li><li>Université de Bordeaux</li></orgName></list><tree><country name="France"><noRegion><name sortKey="Pelissero, C" sort="Pelissero, C" uniqKey="Pelissero C" first="C." last="Pelissero">C. Pelissero</name></noRegion><name sortKey="Babin, P" sort="Babin, P" uniqKey="Babin P" first="P." last="Babin">P. Babin</name><name sortKey="Bennetau, B" sort="Bennetau, B" uniqKey="Bennetau B" first="B." last="Bennetau">B. Bennetau</name><name sortKey="Dunogues, J" sort="Dunogues, J" uniqKey="Dunogues J" first="J." last="Dunogues">J. 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