School of Life Sciences, Nanjing Normal University, Nanjing 210023, People's Republic of China; School of Food Science, Nanjing Xiaozhuang University, Nanjing 211171, People's Republic of China; Jiangsu Provincial Key Construction Laboratory of Special Biomass Byproduct Resource Utilization, Nanjing 211171, People's Republic of China.
School of Food Science, Nanjing Xiaozhuang University, Nanjing 211171, People's Republic of China; Jiangsu Provincial Key Construction Laboratory of Special Biomass Byproduct Resource Utilization, Nanjing 211171, People's Republic of China.
Int J Biol Macromol. 2019 May 1;128:363-375. doi: 10.1016/j.ijbiomac.2019.01.141. Epub 2019 Jan 25.
In the current study, serum metabolomics techniques were used to evaluate the potential mechanism of the effect of chicory polysaccharides in non-alcoholic fatty liver disease (NAFLD) rats. A rat model of NAFLD was constructed according to the histopathological data and biochemical parameters, while the underlying mechanisms of high-fat diet (HFD) induced NAFLD and the therapeutic effects of chicory polysaccharides (CP) were studied by the adoption of serum metabolomics. The serum metabolites were analyzed by GC/MS. Multivariate statistical approaches such as principal component analysis, revealed significant differences with HFD model and CP groups against the control. Results indicated that CP plays a regulatory role in the occurrence of NAFLD. Meantime, a total of 65 candidate biomarkers were screened and identified. Cluster analysis, enrichment analysis and metabolic pathway analysis of differential metabolites also indicated that amino acid metabolism and fatty acid biosynthesis in NAFLD rats, the β-oxidation and urea cycle of very long-chain fatty acids were mainly disturbed when compared against the control group. The corresponding metabolic pathways in the CP group were relieved compared against the NAFLD rats. These results showed that untargeted metabonomics helps to explain intervention effects of chicory polysaccharide with the rat model of NAFLD.
在本研究中,采用血清代谢组学技术评估菊苣多糖对非酒精性脂肪性肝病(NAFLD)大鼠作用的潜在机制。根据组织病理学数据和生化参数构建了大鼠 NAFLD 模型,通过采用血清代谢组学研究高脂肪饮食(HFD)诱导的 NAFLD 的潜在机制和菊苣多糖(CP)的治疗效果。通过 GC/MS 分析血清代谢物。采用主成分分析等多变量统计方法,发现 HFD 模型组和 CP 组与对照组有显著差异。结果表明 CP 在 NAFLD 的发生中发挥调节作用。同时,筛选并鉴定了 65 种候选生物标志物。差异代谢物的聚类分析、富集分析和代谢途径分析也表明,与对照组相比,NAFLD 大鼠的氨基酸代谢和脂肪酸合成、极长链脂肪酸的β-氧化和尿素循环受到干扰。CP 组的相应代谢途径与 NAFLD 大鼠相比得到缓解。这些结果表明,非靶向代谢组学有助于解释菊苣多糖对 NAFLD 大鼠模型的干预作用。