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Metabolomics study of the therapeutic mechanism of Schisandra chinensis lignans on aging rats induced by D-galactose

机译:五味子木脂素对D-半乳糖诱发衰老大鼠治疗机制的代谢组学研究

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Objective: The aim of this study was to evaluate the antiaging effect of Schisandra chinensis lignans (SCL) by analyzing the characteristics in the serum of d-galactose (d-gal)-induced rats. Methods: Forty male Wistar rats were randomly divided into control group, d-gal model group, low-dose SCL group (50 mg/kg/d), medium-dose SCL group (100 mg/kg/d), and high-dose SCL group (200 mg/kg/d). A serum metabolomics analysis method based on rapid resolution liquid chromatography coupled with quadruple-time-of-flight mass spectrometry was carried out to study the characteristics of d-gal-induced aging rats and evaluate the antiaging effects of SCL, and multivariate statistical analysis was performed for pattern recognition and characteristic metabolites identification. The relative levels of p19, p53, and p21 genes in the brain tissue were measured by quantitative real-time polymerase chain reaction for investigating the underlying mechanism. Results: Metabolomics analysis showed that 15 biomarkers were identified and 13 of them recovered to the normal levels after the administration of SCL. Based on the pathway analysis, the antiaging mechanisms of SCL might be involved in the following metabolic pathways: energy, amino acid, lipid, and phospholipid metabolism. Furthermore, SCL significantly inhibited the mRNA expression level of p19, p53, and p21 in the brain of aging rats induced by d-gal. Conclusion: These results suggest that SCL can delay rat aging induced by d-gal through multiple pathways.
机译:目的:本研究旨在通过分析d-半乳糖(d-gal)诱导的大鼠血清的特征来评估五味子木脂素(SCL)的抗衰老作用。方法:40只Wistar雄性大鼠随机分为对照组,d-gal模型组,低剂量SCL组(50 mg / kg / d),中剂量SCL组(100 mg / kg / d)和高剂量SCL组。剂量SCL组(200 mg / kg / d)。采用快速拆分液相色谱-飞行时间四次质谱联用的血清代谢组学分析方法,研究了d-gal诱导的衰老大鼠的特征,评价了SCL的抗衰老作用,并进行了多元统计分析。用于模式识别和特征代谢物识别。通过定量实时聚合酶链反应测量脑组织中p19,p53和p21基因的相对水平,以研究其潜在机制。结果:代谢组学分析表明,在SCL给药后,鉴定出15种生物标志物,其中13种恢复到正常水平。根据途径分析,SCL的抗衰老机制可能与以下代谢途径有关:能量,氨基酸,脂质和磷脂代谢。此外,SCL显着抑制d-gal诱导的衰老大鼠脑中p19,p53和p21的mRNA表达水平。结论:这些结果表明,SCL可通过多种途径延缓d-gal诱导的大鼠衰老。

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