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DOI 10.1016/j.fct.2023.114189

Медицинская библиотека · Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2023

Microcystin-LR prenatal exposure drives preeclampsia-like changes in mice by inhibiting the expression of TGF-β and VEGFA.

Guo Meihong, Yan Pinru, Zhu Mengjiao, Choi Manhou, Li Xinrui, Huang Jiahao, Zou Jianghao, Yuan Jintao, Ding Weidong, Li Dongmei, Han Xiaodong, Wang Yong, Wu Jiang

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Аннотация

Microcystin-leucine-arginine (MC-LR) is widespread in the water and food, which has suspected to be associated with adverse pregnancy outcomes. In the present study, we aim to assess the interaction between MC-LR exposure and preeclampsia development and elucidate the molecular events involved. After exposure to MC-LR during pregnancy, the mice developed hypertension and proteinuria, the typical symptoms of preeclampsia. This was associated with decreased invasiveness of placental trophoblast and vascular dysplasia caused by MC-LR through down-regulating VEGFA and TGF-β expression via AKT/m-TOR/HIF-1α pathway. In addition, this conclusion has been confirmed in a case-control study. Significantly, the addition of Deferoxamine (DFM), a phosphorylated serine-threonine protein kinases (p-AKT) specific agonist, can antagonize the inhibitory effect of MC-LR on the expression of related proteins, which further ameliorate the migration and invasion ability of HTR-8/Svneo cells. To sum up, our study revealed the pathologic mechanism by which MC-LR lead to preeclampsia and emphasized the importance of pregnancy management.

Для цитирования: Guo Meihong, Yan Pinru, Zhu Mengjiao, Choi Manhou, Li Xinrui, Huang Jiahao, Zou Jianghao, Yuan Jintao, Ding Weidong, Li Dongmei, Han Xiaodong, Wang Yong, Wu Jiang. Microcystin-LR prenatal exposure drives preeclampsia-like changes in mice by inhibiting the expression of TGF-β and VEGFA.. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2023. DOI: 10.1016/j.fct.2023.114189.

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