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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Integrated renal metabolomic and metallomic profiling revealed protective effect and metabolic mechanism of Gushudan on glucocorticoid-induced osteoporotic rat based on GC-MS and ICP-MS
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Integrated renal metabolomic and metallomic profiling revealed protective effect and metabolic mechanism of Gushudan on glucocorticoid-induced osteoporotic rat based on GC-MS and ICP-MS

机译:综合性肾代和金属谱揭示了基于GC-MS和ICP-MS的Gushocoxcoid诱导的骨质疏松症大鼠的保护作用和代谢机制

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摘要

Based on the traditional Chinese medicine theory, kidney is considered to govern the bones and dominate the store of essence ('jing' in Chinese). Gushudan (GSD) is a traditional Chinese medicine prescription for the treatment osteoporosis in the clinic and is beneficial for improving kidney function and strengthening bone in vivo. This study aims to reveal the renal metabolic profiling of glucocorticoid-induced osteoporosis (GIOP) rats and the potential preventive effect of GSD based on an integrative metabolomic and metallomic approach. Gas chromatography-mass spectrometry (GC-MS) and inductively coupled plasma mass spectrometry (ICP-MS) were combined for the investigation of renal metabolomic and metallomic profiling. In the metabolomic analysis, 17 potential biomarkers were found to be related to GIOP, such as glucose, malate, -y-aminobutyric acid and arachidonic acid. And seven metallic elements, including Zn, Mn, Se, Fe, Mo, As and Ba, were identified in rat kidney tissue in the metallomic analysis. The major metabolic pathways included aerobic glycolysis, and neurotransmitter amino acids metabolism. It was worth mentioning that the levels of trace metal elements (Zn, Mn, Se, Fe, As and Ba) significantly reduced in the model group, while the contents of Zn, Mn, Se, Fe and As were elevated after administration of GSD. Finally, a correlation metabolic regulatory network and the metabolic pathways associated with trace metal elements were further investigated to illuminate the role of potential biomarkers and trace metal elements in GIOP rats. These variations of potential biomarkers and trace metal elements suggested the existence of kidney damage and metabolic disorder in GIOP rats, which indicated a close relationship between bone and kidney in vivo. Moreover, the integrated renal metabolomic and metallomic profiling could be as an effective supplementary measure to the plasma and urine metabolomic research, and it was helpful to further understand the holistic formation process of osetoporosis and the potential preventive effects of GSD on GIOP rats. (C) 2020 Elsevier B.V. All rights reserved.
机译:根据传统中医理论,肾被认为是支配骨骼和主导精髓储存(中文称为“精”)。骨舒丹是临床上治疗骨质疏松症的中药方剂,在体内有利于改善肾功能和增强骨质。本研究旨在揭示糖皮质激素诱导的骨质疏松症(GIOP)大鼠的肾脏代谢特征,以及基于综合代谢组学和金属组学方法的GSD的潜在预防作用。将气相色谱-质谱(GC-MS)和电感耦合等离子体质谱(ICP-MS)相结合,研究肾脏代谢组学和金属组学特征。在代谢组学分析中,发现17个潜在的生物标记物与GIOP有关,如葡萄糖、苹果酸、-y-氨基丁酸和花生四烯酸。在金属组学分析中,在大鼠肾组织中鉴定出七种金属元素,包括锌、锰、硒、铁、钼、砷和钡。主要代谢途径包括有氧糖酵解和神经递质氨基酸代谢。值得一提的是,模型组的微量金属元素(锌、锰、硒、铁、砷和钡)水平显著降低,而服用GSD后,锌、锰、硒、铁和砷的含量升高。最后,进一步研究了与微量金属元素相关的代谢调节网络和代谢途径,以阐明潜在生物标记物和微量金属元素在GIOP大鼠中的作用。这些潜在生物标志物和微量金属元素的变化表明GIOP大鼠存在肾损伤和代谢紊乱,这表明体内骨与肾之间存在密切关系。此外,综合肾脏代谢组学和金属组学分析可作为血浆和尿液代谢组学研究的有效补充措施,有助于进一步了解骨质疏松的整体形成过程以及GSD对GIOP大鼠的潜在预防作用。(C) 2020爱思唯尔B.V.版权所有。

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