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整合肠道微生物群和血清代谢组学揭示草甘膦诱导的小鼠肝损伤。

Integrated gut microbiota and serum metabolomics reveal glyphosate-induced hepatic injury in mice.

作者信息

Li Gang, Cheng Yu, Yang Xiaolei, Chai Zijun, Mu Zhihui, Chao Hong, Li Hongjie, Qi Yanbo, Qi Lei, Liu Jicheng

机构信息

School of Public Health, Qiqihar Medical University, Qiqihar, China.

Postdoctoral Research Station of Qiqihar Institute of Medical Science, Qiqihar, China.

出版信息

Hum Exp Toxicol. 2025 Jan-Dec;44:9603271251326877. doi: 10.1177/09603271251326877. Epub 2025 Mar 11.

Abstract

IntroductionGlyphosate (GLP) is one of the most widely used herbicides in the world. However, its underlying effects on the liver remain unclear. This study aims to investigate the toxic effects and the gut microbiome- and serum metabolite-related mechanisms of GLP on the liver in mice.Methods16S rDNA sequencing and UPLC-Q-TOF-MS/MS were used to investigate the mechanisms of GLP toxicity in mice administered with 0, 50, 250 and 500 mg/kg/day GLP for 30 days.ResultsGLP induced hepatocyte edema and ballooning as well as inflammatory cell infiltration. Exposure to GLP resulted in increased levels of serum ALT, TBIL, DBIL, and GLU. Microbiota analysis at the phylum level demonstrated that the proportions of Patescibacteria decreased in the GLP-treated group. The genus-level analysis identified 11 different genera, with eight decreased and three increased in the GLP-exposed group. Metabolomics analysis of serum showed 42 differential metabolites between the GLP and control groups. The metabolic pathway enrichment analysis revealed that the pentose phosphate pathway (PPP) and pyrimidine metabolism were significantly activated. Spearman analysis showed that the changes in the differential metabolites of the PPP and pyrimidine metabolism and gut microbiota were strongly associated with the biochemical index.DiscussionIn conclusion, GLP exposure induces hepatic injury through alterations in the gut microbiome and metabolic pathways, particularly by activating the pentose phosphate pathway and pyrimidine metabolism.

摘要

引言

草甘膦(GLP)是世界上使用最广泛的除草剂之一。然而,其对肝脏的潜在影响仍不清楚。本研究旨在探讨草甘膦对小鼠肝脏的毒性作用以及与肠道微生物群和血清代谢物相关的机制。

方法

采用16S rDNA测序和超高效液相色谱-四极杆-飞行时间串联质谱(UPLC-Q-TOF-MS/MS)技术,对连续30天给予0、50、250和500 mg/kg/天草甘膦的小鼠进行草甘膦毒性机制研究。

结果

草甘膦诱导肝细胞水肿、气球样变以及炎性细胞浸润。接触草甘膦导致血清谷丙转氨酶(ALT)、总胆红素(TBIL)、直接胆红素(DBIL)和葡萄糖(GLU)水平升高。在门水平上的微生物群分析表明,草甘膦处理组中Patescibacteria的比例下降。属水平分析鉴定出11个不同的属,草甘膦暴露组中有8个减少,3个增加。血清代谢组学分析显示草甘膦组和对照组之间有42种差异代谢物。代谢途径富集分析表明磷酸戊糖途径(PPP)和嘧啶代谢显著激活。Spearman分析表明,PPP和嘧啶代谢的差异代谢物变化以及肠道微生物群与生化指标密切相关。

讨论

总之,草甘膦暴露通过改变肠道微生物群和代谢途径,特别是激活磷酸戊糖途径和嘧啶代谢,诱导肝损伤。

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