Li Meng, Lv Meile, Liu Tingting, Du Gaoyi, Wang Qiangwei
Ministry of Agriculture Key Laboratory of Molecular Biology of Crop Pathogens and Insects, Institute of Pesticide and Environmental Toxicology, Zhejiang University, Hangzhou 310058, China.
College of Fisheries, Huazhong Agricultural University, Wuhan 430070, China.
Environ Sci Technol. 2022 Jun 21;56(12):8463-8474. doi: 10.1021/acs.est.2c00516. Epub 2022 May 12.
Pyrethroids, an effective and widely used class of pesticides, have attracted considerable concerns considering their frequent detection in environmental matrices. However, their potential health risks to amphibians remain unclear. In our study, female were exposed to 0, 0.06, and 0.3 μg/L typical pyrethroid, -bifenthrin (-BF), for 3 months. Elevated activities of both aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were observed, indicating an ongoing liver injury. Furthermore, exposure to -BF led to hyperlipidemia and lipid accumulation in the liver of . The targeted lipidomic analysis further revealed that treatment with -BF perturbed liver steroid homeostasis, as evidenced by the enriched lipids in the steroid biosynthesis pathway. Consistent with the targeted lipidomic result, treatment with -BF changed the liver transcriptome profile with induction of 808 and 1230 differentially expressed genes. Kyoto Encyclopedia of Genes and Genomes analysis underlined the adverse effects of -BF exposure on steroid biosynthesis, primary bile acid biosynthesis, and the PPAR signaling pathway in the liver. Taken together, our study revealed that exposure to -BF at environmentally relevant concentrations resulted in lipid metabolic disorder associated with nonalcoholic fatty liver disease of , and our results provided new insight into the potential long-term hazards of pyrethroids.
拟除虫菊酯是一类有效且广泛使用的杀虫剂,鉴于其在环境基质中频繁被检测到,已引起了相当大的关注。然而,它们对两栖动物的潜在健康风险仍不明确。在我们的研究中,将雌性蟾蜍暴露于0、0.06和0.3μg/L的典型拟除虫菊酯——β-联苯菊酯(β-BF)中,持续3个月。观察到天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)的活性均升高,表明存在持续的肝损伤。此外,暴露于β-BF导致蟾蜍肝脏出现高脂血症和脂质积累。靶向脂质组学分析进一步显示,β-BF处理扰乱了蟾蜍肝脏类固醇稳态,类固醇生物合成途径中脂质的富集证明了这一点。与靶向脂质组学结果一致,β-BF处理改变了蟾蜍肝脏转录组图谱,诱导了808个和1230个差异表达基因。京都基因与基因组百科全书分析强调了β-BF暴露对蟾蜍肝脏类固醇生物合成、初级胆汁酸生物合成以及PPAR信号通路的不利影响。综上所述,我们的研究表明,在环境相关浓度下暴露于β-BF会导致蟾蜍出现与非酒精性脂肪性肝病相关的脂质代谢紊乱,我们的结果为拟除虫菊酯的潜在长期危害提供了新的见解。