首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Effect of ergosta-4,6,8(14),22-tetraen-3-one (ergone) on adenine-induced chronic renal failure rat: A serum metabonomic study based on ultra performance liquid chromatography/high-sensitivity mass spectrometry coupled with MassLynx i-FIT algorithm
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Effect of ergosta-4,6,8(14),22-tetraen-3-one (ergone) on adenine-induced chronic renal failure rat: A serum metabonomic study based on ultra performance liquid chromatography/high-sensitivity mass spectrometry coupled with MassLynx i-FIT algorithm

机译:ergosta-4,6,8(14),22-tetraen-3-one(ergone)对腺嘌呤诱发的慢性肾衰竭大鼠的影响:基于超高效液相色谱/高灵敏度质谱联用的血清代谢组学研究MassLynx i-FIT算法

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Background: Ergosta-4,6,8(14),22-tetraen-3-one (ergone) has been proven to prevent the progression of renal injury and the subsequent renal fibrosis. We investigated the therapeutic effects and mechanism of ergone on a chronic renal failure model of rats induced by adenine. Methods: A serum metabonomic method based on the UPLC Q-TOF/MS was undertaken to explore the excretion pattern of low molecular mass metabolites. Results: Coupled with blood biochemistry and kidney histopathology results, the significant difference in metabolic profiling between adenine-induced chronic renal failure group and the ergone treated group by using pattern recognition analysis indicated that changes in global serum metabolites occurred. Some significantly changed metabolites like lysophosphatidylcholines, adenine, dopamine, creatinine, aspartic acid and phenylalanine have been found and identified. These biochemical changes in serum metabolites are related to the perturbations of amino acid metabolism and lecithin metabolism, which may be helpful to further understand the chronic renal failure and therapeutic mechanisms of ergone. Conclusion: The work shows that the metabonomic method is a valuable tool for studying the essence of chronic kidney disease and therapeutic effect mechanism of preclinical or clinical drug.
机译:背景:Ergosta-4,6,8(14),22-tetraen-3-one(ergone)已被证明可以预防肾损伤的进展和随后的肾纤维化。我们研究了麦角酮对腺嘌呤诱导的大鼠慢性肾衰竭模型的治疗作用和机制。方法:采用基于UPLC Q-TOF / MS的血清代谢组学方法研究低分子量代谢物的排泄方式。结果:结合血液生化和肾脏组织病理学结果,通过模式识别分析,腺嘌呤诱发的慢性肾功能衰竭组和麦角酮治疗组之间代谢谱的显着差异表明整体血清代谢物发生了变化。已经发现并鉴定了一些明显变化的代谢产物,如溶血磷脂酰胆碱,腺嘌呤,多巴胺,肌酐,天冬氨酸和苯丙氨酸。血清代谢产物的这些生化变化与氨基酸代谢和卵磷脂代谢的扰动有关,这可能有助于进一步了解慢性肾功能衰竭和麦角酮的治疗机制。结论:这项工作表明,代谢组学方法是研究慢性肾脏病的实质和临床前或临床药物治疗作用机理的宝贵工具。

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