4.7 Article

Subacute cadmium exposure disrupts the hypothalamic-pituitary-gonadal axis, leading to polycystic ovarian syndrome and premature ovarian failure features in female rats

期刊

ENVIRONMENTAL POLLUTION
卷 269, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.envpol.2020.116154

关键词

Cadmium; Endocrine disruptor chemical; Hypothalamic-pituitary-gonadal (HPG) axis; Polycystic ovary syndrome (PCOS); Premature ovary failure (POF); Uterine abnormalities

资金

  1. FAPES [03/2017-UNIVERSAL, 179/2017]
  2. CNPq [304724/2017-3, 12/2017, 304557/2018-8]
  3. FAPES/CNPq [24/2018, 572/2018, 80600115/2017]
  4. FAPES/CNPq
  5. Bioclin Program (Bioclin-Quibasa)

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This study evaluated the effects of cadmium exposure on the HPG axis and various abnormalities in female rats, finding that cadmium exposure led to metabolic and reproductive dysfunctions, indicating that cadmium disrupts HPG axis function, leading to features of PCOS and POF.
Cadmium (Cd), a toxic heavy metal, is a known endocrine disruptor that is associated with reproductive complications. However, few studies have explored the effects of Cd exposure on features of polycystic ovary syndrome (PCOS) and premature ovary failure (POF). In this study, we assessed whether doses found in workers occupationally exposed to Cd and subacute exposure result in hypothalamic-pituitarygonadal (HPG) axis and other irregularities. We administered CdCl2 to female rats (100 ppm in drinking water for 30 days) and then assessed Cd levels in the blood, HPG axis and uterus. Metabolic features, HPG axis function, reproductive tract (RT) morphophysiology, inflammation, oxidative stress (OS), and fibrosis were evaluated. Cd exposure increased Cd levels in the serum, HPG axis, and uterus. Cd rats displayed metabolic impairments, such as a reduction in adiposity, dyslipidemia, and insulin resistance (IR). Cd exposure also caused improper functioning in the HPG. Specifically, Cd exposure caused irregular estrous cyclicity, abnormal hypothalamic gene expression (upregulated - Kiss1, AR and mTOR; downregulated - Kiss1R, LepR and THE-alpha), high LH levels, low AMH levels and abnormal ovarian follicular development, coupled with a reduction in ovarian reserve and antral follicle number was observed, suggesting ovarian depletion. Further, Cd exposure caused a reduction in corpora lutea (CL) and granulosa layer thickness together with an increase in cystic/atretic follicles. In addition, Cd exposure caused RT inflammation, OS and fibrosis. Finally, strong positive correlations were observed between serum, RT Cd levels, IR, dyslipidemia and estrous cycle length, cystic, atretic follicles, LH levels, and RT inflammation. Thus, these data suggest that subacute Cd exposure using doses found in workers occupationally exposed to Cd disrupt the HPG axis function, leading to PCOS and POF features and other abnormalities in female rats. (C) 2020 Elsevier Ltd. All rights reserved.

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