Zhang Meiling, Bao Shihui, Lin Feiou, Lin Yingying, Zhang Lijing, Xu Mengzhi, Huang Xueli, Wen Congcong, Hu Lufeng, Lin Guanyang
Analytical and Testing Center, Wenzhou Medical University Wenzhou 325035, China.
The Second Affiliated Hospital & Yuying Children's Hospital, Wenzhou Medical University Wenzhou 325000, China.
Int J Clin Exp Med. 2015 Nov 15;8(11):21180-6. eCollection 2015.
This study aimed to evaluate the effect of Datura stramonium on rats by examining the differences in urine and serum metabolites between Datura stramonium groups and control group. SIMCA-P+12.0.1.0 software was used for partial least-squares discriminant analysis (PLS-DA) to screen for the differential metabolites. Fifteen metabolites in urine including malonic acid, pentanedioic acid, D-xylose, D-ribose, xylulose, azelaic acid, threitol, glycine, butanoic acid, D-mannose, D-gluconic acid, galactonic acid, myo-inositol, octadecanoic acid, pseudouridine and ten metabolites in serum including alanine, butanedioic acid, L-methionine, propanedioic acid, hexadecanoic acid, D-fructose, tetradecanoic acid, D-glucose, D-galactose, oleic acid were selected as the characteristic metabolites. The PLS-DA scores plot indicated that serum and urine metabolites have a variety of changes among low dose group, high dose group and control group. These metabolites were related with amino metabolism, lipid metabolism and energy metabolism. The result reflected the relationship between metabolites in rat fluid and Datura stramonium spectra. Potential differences in metabolites and metabolic pathway analysis showed that the establishment of urine and serum metabolomics methods for further evaluating drug has great significance.
本研究旨在通过检测曼陀罗组与对照组大鼠尿液和血清代谢物的差异,评估曼陀罗对大鼠的影响。使用SIMCA-P+12.0.1.0软件进行偏最小二乘判别分析(PLS-DA)以筛选差异代谢物。尿液中的15种代谢物包括丙二酸、戊二酸、D-木糖、D-核糖、木酮糖、壬二酸、苏糖醇、甘氨酸、丁酸、D-甘露糖、D-葡萄糖酸、半乳糖酸、肌醇、十八烷酸、假尿苷,以及血清中的10种代谢物包括丙氨酸、丁二酸、L-甲硫氨酸、丙二酸、十六烷酸、D-果糖、十四烷酸、D-葡萄糖、D-半乳糖、油酸被选为特征代谢物。PLS-DA得分图表明,低剂量组、高剂量组和对照组之间血清和尿液代谢物有多种变化。这些代谢物与氨基酸代谢、脂质代谢和能量代谢有关。结果反映了大鼠体液中代谢物与曼陀罗光谱之间的关系。代谢物的潜在差异和代谢途径分析表明,建立尿液和血清代谢组学方法以进一步评估药物具有重要意义。