Comparison of hormonal activity (estrogen, androgen and progestin) of standardized plant extracts for large scale use in hormone replacement therapy

Verena Beck, E Unterrieder, Liselotte Krenn, Wolfgang Kubelka, Alois Jungbauer (Korresp. Autor*in)

    Veröffentlichungen: Beitrag in FachzeitschriftMeeting Abstract/Conference Paper

    Abstract

    Extracts from red clover (Trifolium pratense), soybean (Glycine max.) and black cohosh (Cimicifuga racemosa) are frequently used as alternative compounds for hormone replacement therapy (HRT) to treat menopausal disorders. Fifteen commercially available products made either from red clover, soybean or black cohosh were tested in in vitro assays in this study. The main polycyclic phenolic compounds of soy and red clover products were biochanin A, genistein, daidzein, formononetin, and glycitein. In red clover products glycitein was not abundant. All the compounds showed clear estrogenic activity through estrogen receptor α (ERα) and estrogen receptor β (ERβ) and affinity to progesterone receptor (PR) and androgen receptor (AR), whereas the compounds from black cohosh did not. This was corroborated by synthetic isoflavones such as biochanin A, daidzein, genistein and formononetin. They exerted affinity to PR and AR in the range of 0.39–110 mM. Statistical analysis applying principal component analysis (PCA) revealed that all red clover and soy products are grouped in different clusters. Red clover products showed a higher affinity to AR and PR than soy products, which is explained by the higher amount of isoflavones present. In vitro assays and chemical analysis showed that theoretical estrogenic activity expressed as equivalent E2 concentration is in the same range as recommended for synthetic estrogens. Broader spectrum of action and hypothesized lower side effects by action through ERβ make them suitable for alternative hormone replacement therapy. © 2003 Elsevier Science Ltd. All rights reserved.
    OriginalspracheEnglisch
    Seiten (von - bis)259-268
    Seitenumfang10
    FachzeitschriftThe Journal of Steroid Biochemistry and Molecular Biology
    Jahrgang84
    Ausgabenummer2-3
    DOIs
    PublikationsstatusVeröffentlicht - 2003

    ÖFOS 2012

    • 3012 Pharmazie, Pharmakologie, Toxikologie

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