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Effects of long-term cadmium exposure on urinary metabolite profiles in mice

机译:长期镉暴露对小鼠尿代谢物谱的影响

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Cadmium (Cd) is a common environmental pollutant with known toxic effects on the kidney. Urinary metabolomics is a promising approach to study mechanism by which Cd-induced nephrotoxicity. The aim of this study was to elucidate the mechanism of Cd toxicity and to develop specific biomarkers by identifying urinary metabolic changes after a long-term of Cd exposure and with the critical concentration of Cd in the kidney. Urine samples were collected from wild-type 129/Sv mice after 67 weeks of 300 ppm Cd exposure and analyzed by ultra performance liquid chromatography connected with quadrupole time of flight mass spectrometer (UPLC-QTOF-MS) based metabolomics approach. A total of 40 most differentiated metabolites (9 down-regulated and 31 up-regulated) between the control and Cd-exposed group were identified. The majority of the regulated metabolites are amino acids (glutamine, L-aspartic acid, phenylalanine, tryptophan, and D-proline) indicating that amino acid metabolism pathways are affected by long-term exposure of Cd. However, there are also some nucleotides (guanosine, guanosine monophosphate, cyclic AMP, uridine), amino acid derivatives (homoserine, N-acetyl-L-aspartate, N-acetylglutamine, acetyl-phenylalanine, carboxymethyllysine), and peptides. Results of pathway analysis showed that the arginine and proline metabolism, purine metabolism, alanine, aspartate and glutamate metabolism, and aminoacyl-tRNA biosynthesis were affected compared to the control. This study demonstrates that metabolomics is useful to elucidate the metabolic responses and biological effects induced by Cd-exposure.
机译:镉(CD)是一种常见的环境污染物,对肾脏具有已知的毒性作用。尿代谢组学是一种有希望的方法来研究CD诱导的肾毒性。本研究的目的是阐明CD毒性的机制,并通过鉴定长期CD暴露后的尿代谢变化和肾脏中的CD临界浓度来发展特异性生物标志物。在300ppm CD暴露的67周后,从野生型129 / SV小鼠中收集尿液样品,并通过与基于飞行质谱仪(UPLC-QTOF-MS)的四极其相连的超级性能液相色谱分析。鉴定了对照和CD曝光组之间的总共40个最分化的代谢物(9个下调和31个上调)。大多数受调节的代谢物是氨基酸(谷氨酰胺,L-天冬氨酸,苯丙氨酸,色氨酸和D-脯氨酸),表明氨基酸代谢途径受CD长期暴露的影响。然而,还有一些核苷酸(鸟苷,鸟苷,单磷酸,环状,尿苷),氨基酸衍生物(均静脉,N-乙酰-1-天冬氨酸,N-乙酰基谷氨酰胺,乙酰苯丙胺,羧甲基氰基)和肽。途径分析结果表明,与对照相比,对精氨酸和脯氨酸代谢,嘌呤代谢,丙氨酸,天冬氨酸和谷氨酸代谢和氨基酰基-TRNA生物合成。本研究表明,代谢组学可用于阐明CD暴露诱导的代谢反应和生物学作用。

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