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使用1H NMR和HPLC-TOF/MS对大鼠氯化汞生化效应进行的代谢组学研究:肾毒性导致内源性代谢物尿液谱的时间依赖性变化。

A metabonomic investigation of the biochemical effects of mercuric chloride in the rat using 1H NMR and HPLC-TOF/MS: time dependent changes in the urinary profile of endogenous metabolites as a result of nephrotoxicity.

作者信息

Lenz E M, Bright J, Knight R, Wilson I D, Major H

机构信息

Department of Drug Metabolism and Pharmacokinetics, AstraZeneca Pharmaceuticals, Mereside, Alderley Park, Macclesfield, UK SK10 4TG.

出版信息

Analyst. 2004 Jun;129(6):535-41. doi: 10.1039/b400159c. Epub 2004 Apr 21.

Abstract

The effects of the administration of a single dose of the model nephrotoxin mercuric chloride (2.0 mg kg(-1), subcutaneous) to male Wistar-derived rats on the urinary metabolite profiles of a range of endogenous metabolites has been investigated using (1)H NMR and HPLC-MS. Urine samples were collected daily for 9 days from both dosed and control animals. Analysis of these samples revealed marked changes in the pattern of endogenous metabolites as a result of HgCl(2) toxicity. Peak disturbances in the urinary metabolite profiles were observed (using both NMR and HPLC-MS) at 3 days post dose. Thereafter the urinary metabolite profile gradually returned to a more normal composition. Markers of toxicity identified by (1)H NMR spectroscopy were raised concentrations of lactate, alanine, acetate, succinate, trimethylamine (TMA), and glucose. Reductions in the urinary excretion of citrate and alpha-ketoglutarate were also seen. Markers identified by HPLC-MS, in positive ion mode, were kynurenic acid, xanthurenic acid, pantothenic acid and 7-methylguanine which decreased after dosing. In addition an ion at m/z 188, probably 3-amino-2-naphthoic acid, was observed to increase after dosing. As well as these identified compounds other ions at m/z 297 and 267 decreased after dosing. In negative ion mode a range of sulfated compounds were observed, including phenol sulfate and benzene diol sulfate, which decreased after dosing. As well as the sulfated components an unidentified glucuronide at m/z 326 was also observed to decrease after dosing. The results of this study demonstrate the complementary nature of the NMR and MS-based techniques for metabonomic analysis.

摘要

已使用¹H NMR和HPLC-MS研究了给雄性Wistar衍生大鼠单次注射模型肾毒素氯化汞(2.0 mg kg⁻¹,皮下注射)对一系列内源性代谢物尿液代谢物谱的影响。从给药动物和对照动物中每天收集尿液样本,持续9天。对这些样本的分析显示,由于HgCl₂毒性,内源性代谢物模式发生了显著变化。给药后3天观察到尿液代谢物谱中的峰干扰(使用NMR和HPLC-MS)。此后,尿液代谢物谱逐渐恢复到更正常的组成。通过¹H NMR光谱鉴定的毒性标志物是乳酸、丙氨酸、乙酸盐、琥珀酸盐、三甲胺(TMA)和葡萄糖的浓度升高。还观察到柠檬酸盐和α-酮戊二酸的尿排泄减少。通过HPLC-MS在正离子模式下鉴定的标志物是犬尿酸、黄尿酸、泛酸和7-甲基鸟嘌呤,给药后它们减少。此外,观察到m/z 188处的离子(可能是3-氨基-2-萘甲酸)给药后增加。除了这些鉴定出的化合物外,m/z 297和267处的其他离子给药后减少。在负离子模式下观察到一系列硫酸化化合物,包括硫酸苯酚和硫酸苯二醇,给药后它们减少。除了硫酸化成分外,还观察到m/z 326处未鉴定的葡糖醛酸苷给药后减少。本研究结果证明了基于NMR和MS的代谢组学分析技术的互补性。

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