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首页> 外文期刊>Frontiers in Physiology >Identification of Serum-Based Metabolic Feature and Characteristic Metabolites in Paraquat Intoxicated Mouse Models
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Identification of Serum-Based Metabolic Feature and Characteristic Metabolites in Paraquat Intoxicated Mouse Models

机译:鉴别血清基于代谢特征和百草枯毒鼠模型特征代谢物

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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. Clostridium botulinum and Peptostreptococcus anaerobius 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.
机译:百草枯(PQ)是一种广泛使用的除草剂,可引起人类的高死亡率。然而,相对较少的研究重点关注PQ毒理的代谢特征来调查潜在机制。在这里,我们通过气相色谱运动时间质谱(GC-TOF / MS)对急性和慢性PQ醉酒小鼠模型进行血清样品的非针对性代谢物质分析,以鉴定急性和慢性PQ中毒的代谢特征和特征代谢物。结果表明,急性PQ中毒后,甘氨酸3-吲哚甲酸(IPA)和甘氨酸,丝氨酸和苏氨酸代谢的途径; 2-羟基丁酸和L-甘露/甘氨酸的比例在急性和慢性PQ中毒之间具有重要意义。然后通过液相色谱 - 质谱(LC-MS)分析进行靶向代谢物分析,以确认急性PQ中毒后IPA的变化。此外,通过QRT-PCR定量粪便中产生粪便的IPA肠道细菌,以解释各种IPA血清浓度。在急性PQ中毒后显着抑制了Clostridium botulinum和Peptostrophococcus Anaerobius。数据表明PQ通过抑制抗氧化代谢物产生肠细菌而部分地引起氧化损伤。总之,我们确定了急性和慢性PQ中毒的特征代谢物和途径,这可能是潜在的生物标志物和治疗靶标。

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