[Impact of arsenic exposure on the hepatic metabolic molecular network in obese pregnant mice using metabolomics and proteomics].

Li-Jing Cai, Yan Wang, Jun-Feng Tan, Hai-Xia Zhou, Shi-Jia Liang, Yan Wu, Jie Zhang
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Abstract

Arsenic is a ubiquitous environmental toxin that can affect normal physiological processes. Although the health impacts of arsenic have been investigated, its influence on hepatic metabolism in obese pregnant women and the underlying mechanisms remain unclear. Multi-omics analysis, including metabolomics and proteomics, can improve the understanding of arsenic-induced hepatotoxicity in obese pregnant women. This study aimed to investigate the adverse effects of gestational arsenic exposure on hepatic metabolism in high-fat-diet-induced obese pregnant mice. Following arsenic exposure during pregnancy, the liver tissue was evaluated comprehensively using metabolomics and proteomics techniques combined with pathological and biochemical analyses. Arsenic exposure not only significantly increased lipid accumulation in the livers of obese pregnant mice but also elevated inflammatory factors and oxidative stress markers. Specifically, histopathological examination revealed more steatosis, inflammatory cell infiltration, and hepatocyte ballooning in the livers of arsenic-exposed mice than in those of controls. These changes indicate that arsenic exposure exacerbates hepatic lipid accumulation and induces liver damage in the context of obesity. Metabolomic analysis provided further insight into the metabolic-level disruption caused by arsenic exposure. Significant changes were observed in lipid metabolism pathways, particularly the arachidonic acid metabolism pathway. As arachidonic acid and its metabolites play important roles in inflammation and oxidative stress, this pathway may be critical in arsenic-induced hepatotoxicity. Additionally, proteomic analysis showed differences in the expression levels of several key proteins involved in lipid synthesis, oxidative stress, and inflammatory response. Notably, oxidative-stress-related proteins, including glutathione peroxidase 4 (GPX4), were upregulated, suggesting an increased oxidative burden. In summary, there are complex interaction mechanisms among arsenic exposure, inflammatory response, and related lipid metabolism. The integration of metabolomics and proteomics aided in clarifying the molecular alterations induced by arsenic. The results show that arsenic exposure significantly affects hepatic lipid metabolism in obese pregnant mice through multiple metabolic pathways and protein regulatory mechanisms. In addition to providing new insights into the relationship between arsenic exposure and obesity as well as related metabolic diseases, this study can act as a reference for environmental health risk assessment and the formulation of public health policies. This enhanced understanding of the adverse effects of arsenic on hepatic metabolism will contribute to the development of strategies for mitigating the health risks associated with environmental toxins, particularly for vulnerable groups such as obese pregnant women.

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[利用代谢组学和蛋白质组学研究砷暴露对肥胖孕鼠肝脏代谢分子网络的影响]。
砷是一种普遍存在的环境毒素,可以影响正常的生理过程。虽然砷对健康的影响已被调查,但其对肥胖孕妇肝脏代谢的影响及其潜在机制尚不清楚。多组学分析,包括代谢组学和蛋白质组学,可以提高对肥胖孕妇砷诱导的肝毒性的认识。本研究旨在探讨妊娠期砷暴露对高脂饮食诱导的肥胖孕鼠肝脏代谢的不良影响。妊娠期砷暴露后,采用代谢组学和蛋白质组学技术结合病理和生化分析对肝组织进行综合评估。砷暴露不仅显著增加肥胖孕鼠肝脏脂质积累,而且升高炎症因子和氧化应激标志物。具体而言,组织病理学检查显示,与对照组相比,砷暴露小鼠肝脏脂肪变性、炎症细胞浸润和肝细胞球囊增加。这些变化表明,在肥胖的情况下,砷暴露加剧了肝脏脂质积累并诱发肝损伤。代谢组学分析为砷暴露引起的代谢水平破坏提供了进一步的见解。脂质代谢途径,尤其是花生四烯酸代谢途径发生了显著变化。由于花生四烯酸及其代谢物在炎症和氧化应激中发挥重要作用,该途径可能在砷诱导的肝毒性中起关键作用。此外,蛋白质组学分析显示,参与脂质合成、氧化应激和炎症反应的几个关键蛋白的表达水平存在差异。值得注意的是,包括谷胱甘肽过氧化物酶4 (GPX4)在内的氧化应激相关蛋白上调,表明氧化负担增加。综上所述,砷暴露、炎症反应和相关脂质代谢之间存在复杂的相互作用机制。代谢组学和蛋白质组学的结合有助于澄清砷诱导的分子改变。结果表明,砷暴露通过多种代谢途径和蛋白质调控机制显著影响肥胖孕鼠肝脏脂质代谢。本研究不仅为砷暴露与肥胖及相关代谢性疾病的关系提供了新的认识,还可为环境健康风险评估和公共卫生政策的制定提供参考。对砷对肝脏代谢的不利影响的进一步了解将有助于制定战略,减轻与环境毒素有关的健康风险,特别是对肥胖孕妇等弱势群体。
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