Hu Hui, DU Yu
/ ( 610041) Department of Emergency and Critical Care Medicine,West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu 610041, China.
/ ( 610041) Department of Occupational and Environmental Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu 610041, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2023 Nov 20;54(6):1219-1226. doi: 10.12182/20231160601.
To analyze the plasma metabolomic features of patients suffering from acute diquat (DQ) poisoning and to explore the molecular mechanism and potential biomarkers of DQ poisoning.
A total of 7 patients suffering from acute DQ poisoning were enrolled in the DQ poisoning group. The poisoning of these patients occurred within a 12-h window at the time of enrollment. Meanwhile, 7 healthy immediate family members of the patients were enrolled as the normal controls. Liquid chromatography-mass spectrometry (LC-MS) was used to perform non-targeted metabolomic profiling of the plasma samples and to screen and identify differential metabolites and metabolic pathways.
A total of 104 metabolites were screened and identified (<0.05 and the variable importance in the projection [VIP]>1). Compared with those of the control group, 61 metabolites, such as sorbitol and galactitol, were up-regulated, and 43 metabolites, such as myo-inositol and gamma-glutamylcysteine, were down-regulated in the DQ poisoning group. Pathway enrichment analysis revealed changes in 11 metabolic pathways, including those for galactose metabolism and linoleic acid metabolism (<0.05).
Metabolomics analysis of plasma samples from DQ poisoning patients shows that DQ mainly interferes with the metabolism of energy, amino acids, and lipids, thus causing metabolic disorders. Some potential biomarkers closely associated with oxidative stress and organ damage of the liver, kidney, and nervous system have been identified.
分析急性敌草快(DQ)中毒患者的血浆代谢组学特征,探讨DQ中毒的分子机制及潜在生物标志物。
将7例急性DQ中毒患者纳入DQ中毒组。这些患者在入组时中毒发生在12小时内。同时,将7名患者的健康直系亲属作为正常对照。采用液相色谱 - 质谱联用(LC - MS)技术对血浆样本进行非靶向代谢组学分析,筛选并鉴定差异代谢物及代谢途径。
共筛选并鉴定出104种代谢物(<0.05且投影中变量重要性[VIP]>1)。与对照组相比,DQ中毒组中有61种代谢物上调,如山梨醇和半乳糖醇;43种代谢物下调,如肌醇和γ-谷氨酰半胱氨酸。通路富集分析显示11条代谢途径发生变化,包括半乳糖代谢和亚油酸代谢途径(<0.05)。
对DQ中毒患者血浆样本进行代谢组学分析表明,DQ主要干扰能量、氨基酸和脂质代谢,从而导致代谢紊乱。已鉴定出一些与氧化应激及肝、肾、神经系统器官损伤密切相关的潜在生物标志物。