Maternal exposure to E 551 during pregnancy leads to genome-wide DNA methylation changes and metabolic disorders in the livers of pregnant mice and their fetuses

被引:5
作者
Zhan, Yingqi [1 ]
Lou, He [1 ]
Shou, Rongshang [1 ]
Li, Anyao [1 ]
Shang, Jiaxin [1 ]
Jin, Yanyan [1 ]
Li, Lu [1 ,2 ]
Zhu, Lidan [1 ]
Lu, Xiaoyan [1 ,3 ,4 ]
Fan, Xiaohui [1 ,2 ,3 ,4 ]
机构
[1] Zhejiang Univ, Pharmaceut Informat Inst, Coll Pharmaceut Sci, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Innovat Ctr Yangtze River Delta, Natl Key Lab Chinese Med Modernizat, Jiaxing 314102, Peoples R China
[3] Westlake Lab Life Sci & Biomed, Hangzhou 310058, Peoples R China
[4] Zhejiang Univ, Jinhua Inst, Jinhua 321016, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
E; 551; Pregnancy; Epigenetics; DNA methylation; Hepatic metabolic disorders; SYNTHETIC AMORPHOUS SILICA; INSULIN-RESISTANCE; SILVER NANOPARTICLES; GESTATIONAL EXPOSURE; DIABETES-MELLITUS; TOXICITY; FOOD; BIODISTRIBUTION; COMPLICATIONS; NANOMATERIAL;
D O I
10.1016/j.jhazmat.2023.133233
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The widespread use of nanoparticles in the food industry has raised concerns regarding their potential adverse effects on human health, particularly in vulnerable populations, including pregnant mothers and fetuses. However, studies evaluating the reproductive and developmental toxicity of food-grade nanomaterials are limited. This study investigated the potential risks of prenatal dietary exposure to food-grade silica nanoparticles (E 551) on maternal health and fetal growth using conventional toxicological and epigenetic methods. The results showed that prenatal exposure to a high-dose of E 551 induces fetal resorption. Moreover, E 551 significantly accumulates in maternal and fetal livers, triggering a hepatic inflammatory response. At the epigenetic level, global DNA methylation is markedly altered in the maternal and fetal livers. Genome-wide DNA methylation sequencing revealed affected mCG, mCHG, and mCHH methylation landscapes. Subsequent bioinformatic analysis of the differentially methylated genes suggests that E 551 poses a risk of inducing metabolic disorders in maternal and fetal livers. This is further evidenced by impaired glucose tolerance in pregnant mice and altered expression of key metabolism-related genes and proteins in maternal and fetal livers. Collectively, the results of this study highlighted the importance of epigenetics in characterizing the potential toxicity of maternal exposure to food-grade nanomaterials during pregnancy.
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页数:19
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