Comparison of developmental toxicity of graphene oxide and graphdiyne to zebrafish larvae

IF 3.9 3区 环境科学与生态学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Wanyan Wu , Weichao Zhao , Chaobo Huang , Yi Cao
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Abstract

Graphdiyne (GDY) is a new member of family of carbon-based 2D nanomaterials (NMs), but the environmental toxicity is less investigated compared with other 2D NMs, such as graphene oxide (GO). In this study, we compared with developmental toxicity of GO and GDY to zebrafish larvae. It was shown that exposure of zebrafish embryos from 5 h post fertilization to GO and GDY for up to 5 days decreased hatching rate and induced morphological deformity. Behavioral tests indicated that GO and GDY treatment led to hyperactivity of larvae. However, blood flow velocity was not significantly affected by GO or GDY. RNA-sequencing data revealed that both types of NMs altered gene expression profiles as well as gene ontology terms and KEGG pathways related with metabolism. We further confirmed that the NMs altered the expression of genes related with lipid droplets and autophagy, which may be account for the delayed development of zebrafish larvae. At the same mass concentrations, GO induced comparable or even larger toxic effects compared with GDY, indicating that GDY might be more biocompatible compared with GO. These results may provide novel understanding about the environmental toxicity of GO and GDY in vivo.

Abstract Image

氧化石墨烯和石墨二炔对斑马鱼幼体发育毒性的比较
石墨炔(GDY)是碳基二维纳米材料(NMs)家族中的新成员,但与氧化石墨烯(GO)等其他二维纳米材料相比,对其环境毒性的研究较少。本研究比较了 GO 和 GDY 对斑马鱼幼体的发育毒性。结果表明,斑马鱼胚胎从受精后 5 小时开始接触 GO 和 GDY 长达 5 天,会降低孵化率并导致形态畸形。行为测试表明,GO 和 GDY 处理会导致幼体过度活跃。然而,血流速度并没有受到 GO 或 GDY 的明显影响。RNA 序列数据显示,这两种 NMs 都改变了基因表达谱以及与新陈代谢相关的基因本体术语和 KEGG 通路。我们进一步证实,NMs 改变了与脂滴和自噬有关的基因的表达,这可能是斑马鱼幼体发育延迟的原因。在相同的质量浓度下,GO 诱导的毒性效应与 GDY 相当甚至更大,这表明 GDY 与 GO 相比可能更具生物相容性。这些结果可能会使人们对 GO 和 GDY 在体内的环境毒性有新的认识。
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来源期刊
CiteScore
7.50
自引率
5.10%
发文量
206
审稿时长
30 days
期刊介绍: Part C: Toxicology and Pharmacology. This journal is concerned with chemical and drug action at different levels of organization, biotransformation of xenobiotics, mechanisms of toxicity, including reactive oxygen species and carcinogenesis, endocrine disruptors, natural products chemistry, and signal transduction with a molecular approach to these fields.
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