Journal
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY
Volume 207, Issue -, Pages -Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ecoenv.2020.111143
Keywords
Graphene oxide; Gut microbiome; Pregnant complication; Placenta barrier
Categories
Funding
- National Natural Science Foundation of China [81773386]
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The study reveals that oral exposure to graphene oxide during gestational period in mice can lead to dose-dependent complications including decreased weight of dam and live fetus, high rate of resorbed embryos and dead fetus, and delayed skeletal development. Additionally, exposure to graphene oxide can result in impaired placenta barrier and dysbiosis of gut microbiome, affecting reproductive outcomes in pregnant mammals. The findings provide valuable evidence to evaluate the reproductive risks of graphene oxide in mammals.
The wide use of graphene oxide (GO) has raised increasing concerns about the potential risks to environmental and human health. Recent studies have shown the vital role of gut microbiome in various pathological status or even exogenous exposure, but more detailed understanding about the effects of possible gut microbiome alter-ations under GO exposure on reproductive toxicology evaluations in pregnant mammals remained elusive. Here we found that orally administrated GO daily during gestational day (GD) 7-16 caused dose-dependent pregnant complications of mice on the endpoint (GD19), including decreased weight of dam and live fetus, high rate of resorbed embryos and dead fetus, and skeletal development retardation. Meanwhile in placenta tissues of pregnant mice exposed to GO at dose over 10 mg/kg, the expression levels of tight junctions (Claudin1 and Occludin) and vascular endothelial growth factor (VEGFA) decreased approximately by 30%-80%, meaning impaired placenta barrier. According to the data of fecal 16s RNA sequencing in 40 mg/kg dose group and the control group, gut microbiome showed dramatically decreased alpha and beta-diversity, and upregulated Firmicutes/ Bacteroidetes ratio owing to GO exposure. What's more, significantly differentiated abundance of Euryarchaeota is expected to be a special biomarker for failed pregnancy caused by GO. Notably, the result of Spearman correlation analysis suggested that there was a strong link (correlation coefficient>0.6) between perturbed gut microbiome with both abnormally expressed factors of placenta barrier and adverse pregnant outcomes. In summary, the damages of GO exposure to placenta barrier and pregnancy were dose-dependent. And GO exposure was responsible for gut microbiome dysbiosis in mice with pregnant complications. These findings could provide referable evidence to evaluate reproductive risk of GO to mammals.
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