Applicability of the OECD 455 in-vitro assay for determination of hERa agonistic activity of isoflavonoids

被引:12
作者
Skledar, Darja Gramec [1 ]
Tvrdy, Vaclav [2 ]
Kenda, Masa [1 ]
Zega, Anamarija [1 ]
Pour, Milan [3 ]
Horky, Pavel [3 ]
Mladenka, Premysl [2 ]
Dolenc, Marija Sollner [1 ]
Masic, Lucija Peterlin [1 ]
机构
[1] Univ Ljubljana, Fac Pharm, Askerceva 7, Ljubljana 1000, Slovenia
[2] Charles Univ Prague, Fac Pharm, Dept Pharmacol & Toxicol, Heyrovskeho 1203, Hradec Kralove 50005, Czech Republic
[3] Charles Univ Prague, Fac Pharm, Dept Organ & Bioorgan Chem, Heyrovskeho 1203, Hradec Kralove 50005, Czech Republic
关键词
Flavonoid; Endocrine activity; Estrogenic effect; OECD TG 455; ESTROGEN-RECEPTOR-ALPHA; ENDOCRINE ACTIVITY; BISPHENOL-A; PHYTOESTROGENS; METABOLITES; BETA; BREAST; PHYTOCHEMICALS; ACTIVATION; INHIBITION;
D O I
10.1016/j.taap.2019.114831
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The Organisation for Economic Co-operation and Development (OECD)-validated transactivation assay using the human estrogen receptor alpha (hER alpha) Hela9903 cell line is used for activity evaluation of hERa agonists and antagonists. Due to many advantages, this assay is broadly used as an initial screening process. However, response significantly higher from that of 17-beta estradiol (E2) was observed with phytoestrogens for concentrations commonly above 1 mu M in previous studies. The main aim of this study was thus to ascertain the applicability of OECD protocol 455 for evaluation of estrogenic activity of natural flavonoids, including known phytoestrogens. The estrogenic activities of aglycones as well as of O-methylated and glycosylated flavonoids were evaluated. Supra-maximal luciferase activity was seen for most of the flavonoids tested at concentrations even below 1 mu M. hER alpha-mediated luciferase expression was confirmed with the competition assay specified in OECD protocol 455. However, at concentrations above 1 mu M, non-specific interactions were also observed. Instead of EC50 values, which could not be determined for most of the isoflavonoids tested, the concentrations corresponding to 10% (PC10) and 50% (PC50) of the maximum activity of the positive control, E2, were used for quantitative determination of estrogenic activities. Appropriate evaluation of the data obtained with the current OECD protocol 455 validated assay represents a valuable tool for initial screening of natural flavonoids for estrogenic activity.
引用
收藏
页数:9
相关论文
共 46 条
  • [1] Risk assessment for peri- and post-menopausal women taking food supplements containing isolated isoflavones
    Aguilar, Fernando
    Crebelli, Riccardo
    Di Domenico, Alessandro
    Dusemund, Birgit
    Frutos, Maria Jose
    Galtier, Pierre
    Gott, David
    Gundert-Remy, Ursula
    lambre, Claude
    Leblanc, Jean-Charles
    Lindtner, Oliver
    Moldeus, Peter
    Mortensen, Alicja
    Mosesso, Pasquale
    Parent-Massin, Dominique
    Oskarsson, Agneta
    Stankovic, Ivan
    Waalkens-Berendsen, Ine
    Woutersen, Rudolf Antonius
    Wright, Matthew
    Younes, Maged
    [J]. EFSA JOURNAL, 2015, 13 (10)
  • [2] Widespread occurrence of bisphenol A diglycidyl ethers, p-hydroxybenzoic acid esters (parabens), benzophenone type-UV filters, triclosan, and triclocarban in human urine from Athens, Greece
    Asimakopoulos, Alexandros G.
    Thomaidis, Nikolaos S.
    Kannan, Kurunthachalam
    [J]. SCIENCE OF THE TOTAL ENVIRONMENT, 2014, 470 : 1243 - 1249
  • [3] Feeling Nature's PAINS: Natural Products, Natural Product Drugs, and Pan Assay Interference Compounds (PAINS)
    Baell, Jonathan B.
    [J]. JOURNAL OF NATURAL PRODUCTS, 2016, 79 (03): : 616 - 628
  • [4] Can Invalid Bioactives Undermine Natural Product-Based Drug Discovery?
    Bisson, Jonathan
    McAlpine, James B.
    Friesen, J. Brent
    Chen, Shao-Nong
    Graham, James
    Pauli, Guido F.
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2016, 59 (05) : 1671 - 1690
  • [5] Licorice root components in dietary supplements are selective estrogen receptor modulators with a spectrum of estrogenic and anti-estrogenic activities
    Boonmuen, Nittaya
    Gong, Ping
    Ali, Zulfiqar
    Chittiboyina, Amar G.
    Khan, Ikhlas
    Doerge, Daniel R.
    Helferich, William G.
    Carlson, Kathryn E.
    Martin, Teresa
    Piyachaturawat, Pawinee
    Katzenellenbogen, John A.
    Katzenellenbogen, Benita S.
    [J]. STEROIDS, 2016, 105 : 42 - 49
  • [6] Efficacy of phytoestrogens for menopausal symptoms: a meta-analysis and systematic review
    Chen, M-N.
    Lin, C-C.
    Liu, C-F.
    [J]. CLIMACTERIC, 2015, 18 (02) : 260 - 269
  • [7] Phytoestrogens activate estrogen receptor β1 and estrogenic responses in human breast and bone cancer cell lines
    Chrzan, Brian G.
    Bradford, Peter G.
    [J]. MOLECULAR NUTRITION & FOOD RESEARCH, 2007, 51 (02) : 171 - 177
  • [8] Damstra Terri., 2002, GLOBAL ASSESSMENT ST, V2nd, P1, DOI DOI 10.1111/J.1469-0691.2012.03873
  • [9] Ability of xeno- and phytoestrogens to modulate expression of estrogen-sensitive genes in rat uterus: estrogenicity profiles and uterotropic activity
    Diel, P
    Schulz, T
    Smolnikar, K
    Strunck, E
    Vollmer, G
    Michna, H
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2000, 73 (1-2) : 1 - 10
  • [10] Evaluation of ligand selectivity using reporter cell lines stably expressing estrogen receptor alpha or beta
    Escande, A
    Pillon, A
    Servant, N
    Cravedi, JP
    Larrea, F
    Muhn, P
    Nicolas, JC
    Cavaillès, V
    Balaguer, P
    [J]. BIOCHEMICAL PHARMACOLOGY, 2006, 71 (10) : 1459 - 1469