Literature DB >> 20002219

Oestrogenic mycotoxin exposures and precocious pubertal development.

F Massart1, G Saggese.   

Abstract

Since the 1970s, there has been a worldwide scientific discussion on the potential health consequences of human exposure to endocrine disrupters: many environmentally persistent compounds are oestrogen agonists and/or androgen antagonists. Thus, they can dysregulate the hypothalamic-pituitary-gonadal axis potentially affecting human puberty timing. Zearalenone (ZEA) is a non-steroidal mycotoxin produced by Fusarium species on several grains. Despite its low acute toxicity and carcinogenicity, ZEA exhibits oestrogenic and anabolic properties in several animal species. ZEA food contamination is caused either by direct contamination of grains, fruits and their based-products or by 'carry-over' of mycotoxins in animal tissues, milk and eggs after intake of contaminated feedstuff. In addition, zeranol (alpha-ZAL), a resorcyl lactone derived from ZEA, has been widely used in the USA as a growth promoter to improve fattening rates in cattle. From 1978 to 1984, a great epidemic of premature thelarche and precocious puberty occurred in Puerto Rico. To explain this condition, it was suggested that dairy and meat products could be contaminated with anabolic oestrogens such as ZEA or alpha-ZAL. Subsequently, worldwide other groups have also reported causative associations between oestrogenic mycotoxins and development of early thelarche and/or precocious puberty in exposed children. In addition to animal data, epidemiological studies strongly support the hypothesis that human pubertal development may be induced by foetal/early or prepubertal exposure to oestrogenic compounds. Indeed, ZEA and its metabolites are able to adopt molecular conformation, which sufficiently resembles 17beta-oestradiol to allow it to bind to oestrogen receptors (ERs) in target cells exerting oestrogenic (agonist) actions. In this view, oestrogenic mycotoxins are suspected as triggering factor for precocious pubertal development at least in prepubertal exposed girls.

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Year:  2009        PMID: 20002219     DOI: 10.1111/j.1365-2605.2009.01009.x

Source DB:  PubMed          Journal:  Int J Androl        ISSN: 0105-6263


  25 in total

Review 1.  Endocrine disruptors and the breast: early life effects and later life disease.

Authors:  Madisa B Macon; Suzanne E Fenton
Journal:  J Mammary Gland Biol Neoplasia       Date:  2013-02-17       Impact factor: 2.673

Review 2.  State of the evidence 2017: an update on the connection between breast cancer and the environment.

Authors:  Janet M Gray; Sharima Rasanayagam; Connie Engel; Jeanne Rizzo
Journal:  Environ Health       Date:  2017-09-02       Impact factor: 5.984

3.  Postweaning exposure to dietary zearalenone, a mycotoxin, promotes premature onset of puberty and disrupts early pregnancy events in female mice.

Authors:  Fei Zhao; Rong Li; Shuo Xiao; Honglu Diao; Maria M Viveiros; Xiao Song; Xiaoqin Ye
Journal:  Toxicol Sci       Date:  2013-01-05       Impact factor: 4.849

4.  Circulating zearalenone and its metabolites differ in women due to body mass index and food intake.

Authors:  T Mauro; L Hao; L C Pop; B Buckley; S H Schneider; E V Bandera; S A Shapses
Journal:  Food Chem Toxicol       Date:  2018-04-17       Impact factor: 6.023

5.  Urinary mycoestrogens, body size and breast development in New Jersey girls.

Authors:  Elisa V Bandera; Urmila Chandran; Brian Buckley; Yong Lin; Sastry Isukapalli; Ian Marshall; Melony King; Helmut Zarbl
Journal:  Sci Total Environ       Date:  2011-10-04       Impact factor: 7.963

6.  Hydroxylation of the mycotoxin zearalenone at aliphatic positions: novel mammalian metabolites.

Authors:  Andreas A Hildebrand; Erika Pfeiffer; Andreas Rapp; Manfred Metzler
Journal:  Mycotoxin Res       Date:  2011-09-08       Impact factor: 3.833

7.  Genotoxicity and inactivation of catechol metabolites of the mycotoxin zearalenone.

Authors:  Stefanie C Fleck; Andreas A Hildebrand; Elisabeth Müller; Erika Pfeiffer; Manfred Metzler
Journal:  Mycotoxin Res       Date:  2012-09-27       Impact factor: 3.833

8.  Catechol metabolites of the mycotoxin zearalenone are poor substrates but potent inhibitors of catechol-O-methyltransferase.

Authors:  Erika Pfeiffer; Daniel Wefers; Andreas A Hildebrand; Stefanie C Fleck; Manfred Metzler
Journal:  Mycotoxin Res       Date:  2013-04-05       Impact factor: 3.833

9.  Effects of α-zearalanol on spermatogenesis and sex hormone levels of male mice.

Authors:  Cunxiang Bo; Wei Zhao; Qiang Jia; Zhifeng Yang; Linlin Sai; Fang Zhang; Zhongjun Du; Gongchang Yu; Lin Xie; Zhenling Zhang
Journal:  Int J Clin Exp Med       Date:  2015-11-15

10.  Multigenerational exposure to dietary zearalenone (ZEA), an estrogenic mycotoxin, affects puberty and reproduction in female mice.

Authors:  Fei Zhao; Rong Li; Shuo Xiao; Honglu Diao; Ahmed E El Zowalaty; Xiaoqin Ye
Journal:  Reprod Toxicol       Date:  2014-06-24       Impact factor: 3.143

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