TY - JOUR
T1 - Comparison of hormonal activity (estrogen, androgen and progestin) of standardized plant extracts for large scale use in hormone replacement therapy
AU - Beck, Verena
AU - Unterrieder, E
AU - Krenn, Liselotte
AU - Kubelka, Wolfgang
AU - Jungbauer, Alois
N1 - DOI: 10.1016/S0960-0760(03)00034-7
Coden: JSBBE
Affiliations: Institute of Applied Microbiology, Univ. of Nat. Rsrc./Appl. Life Sci., Muthgasse 18, 1190 Vienna, Austria; Institute of Pharmacognosy, University of Vienna, Althanstraße 14, 1090 Vienna, Austria
Adressen: Jungbauer, A.; Institute of Applied Microbiology; Univ. of Nat. Rsrc./Appl. Life Sci.; Muthgasse 18 1190 Vienna, Austria; email: [email protected]
Source-File: DirschHeringViernsteinScopus_iso.csv
Import aus Scopus: 2-s2.0-0242500490
Importdatum: 29.11.2006 12:36:09
24.08.2007: Datenanforderung 1833 (Import Sachbearbeiter)
22.10.2007: Datenanforderung 1908 (Import Sachbearbeiter)
PY - 2003
Y1 - 2003
N2 - 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.
AB - 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.
U2 - 10.1016/S0960-0760(03)00034-7
DO - 10.1016/S0960-0760(03)00034-7
M3 - Meeting abstract/Conference paper
VL - 84
SP - 259
EP - 268
JO - The Journal of Steroid Biochemistry and Molecular Biology
JF - The Journal of Steroid Biochemistry and Molecular Biology
SN - 0960-0760
IS - 2-3
ER -