Yu Youjia, Gao Zishan, Lou Jiaqian, Mao Zhengsheng, Li Kai, Chu Chunyan, Hu Li, Li Zheng, Deng Chuwei, Fan Hanting, Chen Peng, Huang Huijie, Yu Yanfang, Ding Jingjing, Li Ding, Chen Feng
Department of Forensic Medicine, School of Basic Medical Science, Nanjing Medical University, Nanjing, China.
Clinical Acupuncture and Moxibustion Department, Second School of Clinical Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Front Physiol. 2020 Feb 6;11:65. doi: 10.3389/fphys.2020.00065. eCollection 2020.
Paraquat (PQ) is a widely used herbicide which can cause high mortality to humans. However, relatively few studies focus on metabolic feature of PQ intoxication for investigating the underlying mechanisms. Here we performed non-targeted metabolomics profiling of serum samples from acute and chronic PQ intoxicated mouse models by gas chromatography time-of-flight mass spectrometry (GC-TOF/MS) to identify metabolic feature and characteristic metabolites of acute and chronic PQ intoxication. Results showed that 3-indolepropionic acid (IPA) and pathway of glycine, serine, and threonine metabolism were significantly altered after acute PQ intoxication; 2-hydroxybutyric acid and the ratio of L-serine/glycine were of significance between acute and chronic PQ intoxication. Then targeted metabolomics profiling was conducted by liquid chromatography-mass spectrometry (LC-MS) analysis to confirm the changes of IPA after acute PQ intoxication. Moreover, IPA-producing gut bacteria in feces were quantified by qRT-PCR to explain the varied IPA serum concentration. and were significantly suppressed after acute PQ intoxication. The data suggested that PQ caused oxidative damage partially through suppression of anti-oxidative metabolite producing gut bacteria. In conclusion, we identified characteristic metabolites and pathway of acute and chronic PQ intoxication which could be potential biomarkers and therapeutic targets.
百草枯(PQ)是一种广泛使用的除草剂,可导致人类高死亡率。然而,相对较少的研究关注PQ中毒的代谢特征以探究其潜在机制。在此,我们通过气相色谱-飞行时间质谱(GC-TOF/MS)对急性和慢性PQ中毒小鼠模型的血清样本进行非靶向代谢组学分析,以确定急性和慢性PQ中毒的代谢特征和特征性代谢物。结果显示,急性PQ中毒后,3-吲哚丙酸(IPA)以及甘氨酸、丝氨酸和苏氨酸代谢途径发生显著改变;急性和慢性PQ中毒之间,2-羟基丁酸以及L-丝氨酸/甘氨酸的比值具有显著性差异。然后通过液相色谱-质谱(LC-MS)分析进行靶向代谢组学分析,以确认急性PQ中毒后IPA的变化。此外,通过qRT-PCR对粪便中产生IPA的肠道细菌进行定量,以解释血清中IPA浓度的变化。急性PQ中毒后,[具体细菌名称1]和[具体细菌名称2]受到显著抑制。数据表明,PQ部分通过抑制产生抗氧化代谢物的肠道细菌而导致氧化损伤。总之,我们确定了急性和慢性PQ中毒的特征性代谢物和途径,它们可能是潜在的生物标志物和治疗靶点。