4.6 Article

Early Postnatal Genistein Administration Affects Mice Metabolism and Reproduction in a Sexually Dimorphic Way

期刊

METABOLITES
卷 11, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/metabo11070449

关键词

phytoestrogens; endocrine disruptor; dimorphism; obesity; kisspeptin; POMC; orexin

资金

  1. COST (European Cooperation in Science and Technology) Action [BM1105]
  2. Fondazione Cavalieri Ottolenghi
  3. Ministero dell'Istruzione, dell'Universita e della Ricerca-MIUR project Dipartimenti di Eccellenza 2018-2022
  4. University of Torino
  5. [PSI2014-57362-P]
  6. [PSI2017-86396-P]

向作者/读者索取更多资源

The study found that early exposure of mice to the phytoestrogen genistein can lead to long-term sex-specific organizational effects, impairing the reproductive system and causing an obesogenic effect only in females. This is likely due to alterations in neuroendocrine circuits controlling metabolism.
The phytoestrogen genistein (GEN) may interfere with permanent morphological changes in the brain circuits sensitive to estrogen. Due to the frequent use of soy milk in the neonatal diet, we aimed to study the effects of early GEN exposure on some physiological and reproductive parameters. Mice of both sexes from PND1 to PND8 were treated with GEN (50 mg/kg body weight, comparable to the exposure level in babies fed with soy-based formulas). When adult, we observed, in GEN-treated females, an advanced pubertal onset and an altered estrous cycle, and, in males, a decrease of testicle weight and fecal testosterone concentration. Furthermore, we observed an increase in body weight and altered plasma concentrations of metabolic hormones (leptin, ghrelin, triiodothyronine) limited to adult females. Exposure to GEN significantly altered kisspeptin and POMC immunoreactivity only in females and orexin immunoreactivity in both sexes. In conclusion, early postnatal exposure of mice to GEN determines long-term sex-specific organizational effects. It impairs the reproductive system and has an obesogenic effect only in females, which is probably due to the alterations of neuroendocrine circuits controlling metabolism; thus GEN, should be classified as a metabolism disrupting chemical.

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