Transcriptomic analysis reveals potential mechanisms of toxicity in a combined exposure to dibutyl phthalate and diisobutyl phthalate in zebrafish (Danio rerio) ovary

斑马鱼 邻苯二甲酸二丁酯 小桶 邻苯二甲酸盐 毒性 转录组 卵巢 生物 卵母细胞 生殖毒性 发育毒性 男科 达尼奥 内分泌干扰物 药理学 化学 细胞生物学 激素 内分泌学 基因 生物化学 内分泌系统 遗传学 基因表达 胚胎 医学 有机化学 妊娠期 怀孕
作者
Hui Chen,Weiwei Feng,Kun Chen,Xuchun Qiu,Hai Xu,Guanghua Mao,Ting Zhao,Yangyang Ding,Xiangyang Wu
出处
期刊:Aquatic Toxicology [Elsevier BV]
卷期号:216: 105290-105290 被引量:60
标识
DOI:10.1016/j.aquatox.2019.105290
摘要

Phthalate esters (PAEs), which are notable plasticizers, can be prolific contaminants in aquatic environments, and have been shown to induce reproductive toxicity. However, the studies concerning their toxicity towards aquatic species are based on individual chemicals, and the combined toxicity of PAEs to aquatic organisms remains unclear. The aim of this study was to explore the potential toxicity mechanisms associated with combined exposure to dibutyl phthalate (DBP) and diisobutyl phthalate (DiBP) in adult female zebrafish ovaries. Zebrafish were exposed to DBP, DiBP and their mixtures for 30 days, and their effects on ovarian histology, plasma sex hormones and ovarian transcriptomics were investigated. Plasma estradiol (E2) levels were significantly decreased by 38.9% in the DBP-1133 exposure group and 41.0% in the DiBP-1038 exposure group. The percentage of late/mature oocytes was also significantly decreased by 17.3% under DBP-1133 exposure and 16.2% under DiBP-1038 exposure, while that under combined exposure was not significantly affected. Nevertheless, transcriptome sequencing revealed 2564 differentially expressed genes (DEGs) in zebrafish ovaries after exposure to the mixtures. Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that the DEGs were involved in the neuroactive ligand-receptor interaction, GnRH, progesterone-mediated oocyte maturation, oocyte meiosis and steroid hormone biosynthesis signaling pathways. These results revealed that combined exposure exerts potential reproductive toxicity at the molecular level.
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