4.2 Article

Cadmium-induced preeclampsia-like phenotype in the rat is related to decreased progesterone synthesis in the placenta

Journal

XENOBIOTICA
Volume 52, Issue 6, Pages 625-632

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/00498254.2022.2124204

Keywords

Preeclampsia; cadmium; progesterone; placenta; rat

Funding

  1. Wenzhou Municipal Science and Technology Bureau [Y20180025]
  2. Key Projects of National Natural Science Foundation of Zhejiang Province [LY20H040004]

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In this study, we found that exposure to cadmium in pregnant rats can lead to the development of preeclampsia-like symptoms, including hypertension, albuminuria, and fetal growth restriction. Furthermore, cadmium exposure also inhibits the synthesis of progesterone in the placenta, which contributes to the onset of preeclampsia in pregnant rats.
Cadmium (Cd) is a toxic element, which is associated with preeclampsia (PE). We treated pregnant rats with cadmium chloride from gestational days (GDs) 9-12 to introduce the PE-like animal model. Maternal systolic blood pressures (SBPs) and body weights were measured on GDs 0, 5, 10, 15, and 20. Foetuses were delivered by Caesarean section on GD20. Then, the dams were sacrificed and the specimens were obtained. The morphological analysis of the placentae was carried out by haematoxylin and eosin staining examination and immunohistochemistry assay. Our study showed that Cd-treated rats developed PE-like phenotypes, such as hypertension, albuminuria, and foetal growth restriction. Moreover, Cd-injected rats displayed abnormal placental angiogenesis and lower progesterone (P4) levels. We further demonstrated that Cd also inhibited the mRNA and protein expressions of steroidogenic acute regulatory protein, cytochrome P450 cholesterol side-chain cleavage enzyme (CYP11A1), and 3 beta-hydroxysteroid dehydrogenase 1 (3 beta-HSD1), which are involved in P4 synthesis in the rat placenta. Our study demonstrates that maternal Cd exposure disrupts the local synthesis of P4 in the placenta, which contributes to the onset of PE in pregnant rats. Supplementing P4 at the early gestational stage may be a promising therapeutic strategy to prevent PE, which requires further investigation.

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