College of Environment and Resource, Research Center of Environment and Health, Shanxi University, Shanxi 030006, PR China.
School of Life Science, Shanxi University, Shanxi 030006, PR China.
Sci Total Environ. 2024 Nov 15;951:175477. doi: 10.1016/j.scitotenv.2024.175477. Epub 2024 Aug 14.
Ozone (O), a persistent pollutant, poses a significant health threat. However, research on its multigenerational toxicity remains limited. Leveraging the Drosophila model with its short lifespan and advanced genetic tools, we explored the effects of O exposure across three generations of fruit flies. The findings revealed that O disrupted motility, body weight, stress resistance, and oxidative stress in three generations of flies, with varying effects observed among them. Transcriptome analysis highlighted the disruption of glucose metabolism-related pathways, encompassing gluconeogenesis/glycolysis, galactose metabolism, and carbon metabolism. Hub genes were identified, and RT-qPCR results indicated that O decreased their transcription levels. Comparative analysis of their human orthologs was conducted using Comparative Toxicogenomics Database (CTD) and DisGeNET databases. These genes are linked to various metabolic diseases, including diabetes, hypoglycemia, and obesity. The trehalose content was reduced in F0 generation flies but increased in F1-F2 generations after O exposure. While the trehalase and glucose levels were decreased across F0-F2 generations. TAG synthesis-related genes were significantly upregulated in F0 generation flies but downregulated in F1-F2 generations. The expression patterns of lipolysis-related genes varied among the three generations of flies. Food intake was increased in F0 generation flies but decreased in F1-F2 generations. Moreover, TAG content was significantly elevated in F0 generation flies by O exposure, while it was reduced in F2 generation flies. These differential effects of O across three generations of flies suggest a metabolic reprogramming aimed at mitigating the damage caused by O to flies. The study affirms the viability of employing the Drosophila model to investigate the mechanisms underlying O-induced glucose and lipid metabolism disorders while emphasizing the importance of studying the long-term health effects of O exposure. Moreover, this research highlights the Drosophila model as a viable tool for investigating the multigenerational effects of pollutants, particularly atmospheric pollutants.
臭氧(O)是一种持久性污染物,对健康构成重大威胁。然而,关于其多代毒性的研究仍然有限。利用具有短生命周期和先进遗传工具的果蝇模型,我们研究了臭氧暴露对三代果蝇的影响。研究结果表明,臭氧破坏了三代果蝇的运动能力、体重、抗应激能力和氧化应激,而且它们之间的影响也不同。转录组分析突出了葡萄糖代谢相关途径的破坏,包括糖异生/糖酵解、半乳糖代谢和碳代谢。鉴定了枢纽基因,RT-qPCR 结果表明臭氧降低了它们的转录水平。使用比较毒理学基因组数据库(CTD)和 DisGeNET 数据库对其人类同源物进行了比较分析。这些基因与各种代谢疾病有关,包括糖尿病、低血糖和肥胖症。在 F0 代果蝇中,海藻糖含量减少,但在 O 暴露后 F1-F2 代中增加。而在 F0-F2 代中,海藻糖酶和葡萄糖水平降低。TAG 合成相关基因在 F0 代果蝇中显著上调,但在 F1-F2 代中下调。脂解相关基因的表达模式在三代果蝇中各不相同。F0 代果蝇的食物摄入量增加,但 F1-F2 代果蝇的食物摄入量减少。此外,O 暴露显著增加了 F0 代果蝇的 TAG 含量,而降低了 F2 代果蝇的 TAG 含量。臭氧对三代果蝇的这些不同影响表明,这是一种代谢重编程,旨在减轻臭氧对果蝇造成的损害。这项研究证实了利用果蝇模型来研究臭氧诱导的葡萄糖和脂质代谢紊乱机制的可行性,同时强调了研究臭氧暴露对长期健康影响的重要性。此外,这项研究还强调了果蝇模型作为研究污染物多代效应的一种可行工具的重要性,特别是大气污染物。