Long-term arsenic exposure decreases mice body weight and liver lipid droplets

被引:0
|
作者
Lai, Chengze [1 ,2 ]
Chen, Linkang [1 ]
Zhong, Xiaoting [1 ]
Tian, Xianbing [3 ]
Zhang, Bin [1 ]
Li, Hao [1 ]
Zhang, Guiwei [4 ]
Wang, Liping [5 ]
Sun, Yanqin [6 ]
Guo, Lianxian [1 ,2 ]
机构
[1] Guangdong Med Univ, Sch Publ Hlth, Dongguan Key Lab Publ Hlth Lab Sci, Dongguan 523808, Peoples R China
[2] Guangdong Med Univ, Dongguan Affiliated Hosp 1, Dongguan, Peoples R China
[3] Guangdong Med Univ, Sch Med Technol, Dongguan 523808, Peoples R China
[4] Shenzhen Acad Metrol & Qual Inspect, Shenzhen 518000, Peoples R China
[5] Guangdong Med Univ, Sch Nursing, Dongguan 523808, Peoples R China
[6] Guangdong Med Univ, Sch Basic Med Sci, Dept Pathol, Dongguan 523808, Peoples R China
基金
中国国家自然科学基金;
关键词
Rice arsenicals; Metabolomics; Long-term exposure; Lipid droplets; Gut microbiome; INDUCED OXIDATIVE STRESS; FATTY; METABOLISM; CELL; ACYLCARNITINES; MICROBIOME; TOXICITY; DISEASE; PROTEIN; IMPACT;
D O I
10.1016/j.envint.2024.109025
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Arsenic (As) is a widespread global pollutant, and there is significant controversy surrounding its complex relationship with obesity, primarily focused on short-term exposure. Recognizing the prolonged nature of dietary arsenic exposure, this study involved feeding mice with arsenic-contained food for 14 months. The results showed that mice exposed to arsenic developed a non-alcoholic fatty liver condition, characterized by a light yellow hue on the liver surface and various pathological alterations in the liver cells, including enlarged nuclei, cellular necrosis, inflammatory infiltration, dysfunctional mitochondria, and endoplasmic reticulum disorganization. There were also disruptions in biochemistry indices, with a significant increase in total cholesterol (TC) level and a decrease in high-density lipoprotein (HDL) level. However, some contradictory observations occurred, such as a significant decrease in body weight, triglyceride (TG) level, and the numbers of lipid droplets. Several genes related to lipid metabolism were tested, and a model was used to explain these discrepancies. Besides, examinations of the colon revealed compromised intestinal barrier function and signs of inflammation. Fecal 16S rRNA sequencing and pseudo-targeted metabolomics revealed disruptions in internal homeostasis, such as modules, nodes, connections, and lipid-related KEGG pathways. Fecal targeted metabolomics analyses of short-chain fatty acids (SCFAs) and bile acids (BAs) demonstrated a significant upregulation in three primary bile acids (CA, CDCA, TCDCA), four secondary bile acids (TUDCA, DCA, LCA, GUDCA), and total SCFAs level. Oxidative stress and inflammation were also evident. Additionally, based on correlation analysis and mediation analysis, it was assumed that changes in the microbiota (e.g., Dubosiella) ) can impact the liver metabolites (e.g., TGs) through alterations in fecal metabolites (e.g., LPCs). These findings provide a theoretical reference for the long-term effect of arsenic exposure on liver lipid metabolism.
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页数:14
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