4.7 Article

Zearalenone Promotes Uterine Development of Weaned Gilts by Interfering with Serum Hormones and Up-Regulating Expression of Estrogen and Progesterone Receptors

Journal

TOXINS
Volume 14, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/toxins14110732

Keywords

zearalenone; gilts; uterus; estrogen receptors; progesterone receptor

Funding

  1. Natural Science Foundation of Shandong Province [ZR2021MC048]
  2. Shandong science and technology-based small and medium-sized enterprises innovation capacity improvement project [2022TSGC1275]
  3. Shandong Province Pig Industry Technology System [SDAIT-08-05]

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The study found that ZEA can linearly increase nutrient digestibility and availability, promote the expression of estrogen/progesterone receptors in the uterus and endometrial cells.
In this study, we aimed to assess the effect of diet ZEA on serum hormones, the location and expression of estrogen receptor ER alpha/beta and progesterone receptor (PR) of the uterus in weaned piglets and to reveal the mechanism underneath. A total of 40 healthy weaned gilts were randomly allocated to basal diet supplemented with 0 (Control), 0.5 (ZEA0.5), 1.0 (ZEA1.0) and 1.5 (ZEA1.5) mg ZEA/kg and fed individually for 35 days. Meanwhile, the porcine endometrial epithelial cells (PECs) were incubated for 24 h with ZEA at 0 (Control), 5 (ZEA5), 20 (ZEA20) and 80 (ZEA80) mu mol/L, respectively. The results showed that nutrient apparent digestibility (CP and GE), nutrient apparent availability (ME/GE, BV and NPU), the uterine immunoreactive integrated optic density (IOD), relative mRNA and protein expression of ER-alpha, ER-beta and PR and the relative mRNA and protein expression of ER-alpha and ER-beta in PECs all increased linearly (p < 0.05) with ZEA. Collectively, ZEA can interfere with the secretion of some reproductive hormones in the serum and promote the expression of estrogen/progesterone receptors in the uterus and PECs. All these indicate that ZEA may promote the development of the uterus in weaned gilts through estrogen receptor pathway.

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