4.7 Article

Perinatal exposure to glyphosate or a glyphosate-based formulation disrupts hormonal and uterine milieu during the receptive state in rats

期刊

FOOD AND CHEMICAL TOXICOLOGY
卷 143, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2020.111560

关键词

Glyphosate; Uterus; Implantation; 17 beta-estradiol; Estrogen receptor alpha; Implantation-related genes

资金

  1. UNL [CAIthornD 2016 PIC 50420150100085LI]
  2. Argentine National Agency of Scientific and Technological Promotion (ANPCyT) (PICT 2014) [2125, 1522]
  3. Argentine National Agency of Scientific and Technological Promotion (ANPCyT) (PICT 2016) [0294]
  4. CONICET (PIP 2015) [11220150100338CO]

向作者/读者索取更多资源

We investigated the effects of perinatal exposure to a glyphosate-based herbicide (GBH) or glyphosate alone (Gly) on female fertility and the hormonal and uterine milieu during the preimplantation period. F0 pregnant rats orally received a GBH or Gly in a dose of 2 mg of glyphosate/kg/day from gestational day (GD) 9 until weaning. F1 females were evaluated to determine the reproductive performance on GD19; and the sex steroid serum levels, the expression of estrogen receptor alpha (ER alpha), progesterone receptor (PR) and implantation-related genes on GD5 (preimplantation period). GBH and Gly induced preimplantation losses in F1 rats. GBH and Gly groups exhibited higher 17 beta-estradiol serum levels, without changes in progesterone. Both compounds increased the uterine ER alpha protein expression, with no differences at transcript level; and only Gly decreased PR mRNA expression. Also, GBH and Gly downregulated Hoxa10 and Lif genes, with no difference in Mud/and Areg expression. To conclude, perinatal exposure to a GBH or Gly disrupted critical hormonal and uterine molecular targets during the receptive state, possibly associated with the implantation failures. Overall, similar results were found in GBH- and Gly-exposed rats, suggesting that the active principle might be the main responsible for the deleterious effects.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据