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Downregulations of placental fatty acid transporters during cadmium-induced fetal growth restriction.
Xu, Peng; Guo, Huiqin; Wang, Huan; Lee, Shao Chin; Liu, Ming; Pan, Yongliang; Zheng, Jian; Zheng, Kang; Wang, Huihui; Xie, Yuxin; Bai, Xiaoxia; Liu, Yun; Zhao, Meirong; Wang, Lan.
Afiliación
  • Xu P; School of Life Science, Shanxi University, Taiyuan 030006, China; Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200030, China. Electronic address: xupeng0313@aliyun.com.
  • Guo H; School of Life Science, Shanxi University, Taiyuan 030006, China. Electronic address: 2858851397@qq.com.
  • Wang H; School of Life Science, Shanxi University, Taiyuan 030006, China. Electronic address: 925735531@qq.com.
  • Lee SC; School of Life Science, Shanxi University, Taiyuan 030006, China; School of Life Sciences, Jiangsu Normal University, Xuzhou 221116, China. Electronic address: lee_shao@hotmail.com.
  • Liu M; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China. Electronic address: ming_ing1983@126.com.
  • Pan Y; Key Laboratory of Vector Biology and Pathogen Control of Zhejiang Province, School of Medicine, Huzhou University, Huzhou 313000, China. Electronic address: 02402@zjhu.edu.cn.
  • Zheng J; Department of Cardiopulmonary Function Examination, Shanxi Provincial Cancer Hospital, Taiyuan 030013, China. Electronic address: 3206663193@qq.com.
  • Zheng K; Special Ward, Shanxi Provincial Cancer Hospital, Taiyuan 030013, China. Electronic address: qwezk1980@163.com.
  • Wang H; School of Life Science, Shanxi University, Taiyuan 030006, China. Electronic address: 22930502521@qq.com.
  • Xie Y; School of Life Science, Shanxi University, Taiyuan 030006, China. Electronic address: 805818801@qq.com.
  • Bai X; Women's Hospital, School of Medicine, Zhejiang University, Hangzhou 310006, China. Electronic address: baixiaoxia@zju.edu.cn.
  • Liu Y; Department of Oncology, Fudan University Pudong Medical Center, Shanghai 201300, China. Electronic address: superliuyun@fudan.edu.cn.
  • Zhao M; Key Laboratory of Microbial Technology for Industrial Pollution Control of Zhejiang Province, College of Environment, Zhejiang University of Technology, Hangzhou 310014, China. Electronic address: zhaomr@zjut.edu.cn.
  • Wang L; School of Life Science, Shanxi University, Taiyuan 030006, China. Electronic address: lanwang@sxu.edu.cn.
Toxicology ; 423: 112-122, 2019 07 01.
Article en En | MEDLINE | ID: mdl-31152847
ABSTRACT
Cadmium (Cd) is one of the environmental pollutants, which has multiple toxic effects on fetuses and placentas. Placental fatty acid (FA) uptake and transport are critical for the fetal and placental development. We aimed to analyze the triglyceride (TG) level, the expression patterns of several key genes involved in FA uptake and transport, and the molecular mechanisms for the altered gene expressions in placentas in response to Cd treatment. Our results showed that the placental TG level was significantly decreased in the Cd-exposed placentas. Fatty acid transporting protein 1 (FATP1), FATP6 and fatty acid binding protein 3 (FABP3) were significantly down-regulated in the placentas from Cd-exposed mice. The expression level of phospho-p38 MAPK was increased by Cd treatment, while the protein level of total p38 MAPK remained unchanged. The expression levels of peroxisome proliferator-activated receptor-γ (PPAR-γ) and the hypoxia-inducible factor-1α (HIF-1α) were significantly decreased in the Cd-exposed placentas. The methylation levels of the promoter regions of FATP1, FATP6 and FABP3 showed no significant differences between the treatment and control groups. In addition, the circulating non-esterified fatty acid (NEFA), total cholesterol (TC), and TG levels were not decreased in the maternal serum from the Cd-exposed mice. Therefore, our results suggest Cd exposure dose not reduce the maternal FA supply, but reduces the placental TG level. Cd treatment also downregulates the placental expressions of FATP1, FATP6 and FABP3, respectively associated with p38-MAPK, p38 MAPK/PPAR-γ and HIF-1α pathways.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Placenta / Cadmio / Proteínas de Transporte de Ácidos Grasos / Retardo del Crecimiento Fetal / Intercambio Materno-Fetal Límite: Animals / Female / Humans / Pregnancy Idioma: En Revista: Toxicology Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Placenta / Cadmio / Proteínas de Transporte de Ácidos Grasos / Retardo del Crecimiento Fetal / Intercambio Materno-Fetal Límite: Animals / Female / Humans / Pregnancy Idioma: En Revista: Toxicology Año: 2019 Tipo del documento: Article