UPLC-QTOF-MS-Based Metabolomics Reveal the Effect of Polysaccharides from Danggui-Shaoyao-San in Type 2 Diabetic Male and Female Rats

Xin F, S. L, J. L., Zhi-Bin W
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Abstract

Background: Type 2 Diabetes Mellitus (T2DM) is currently one of the most prominent and global chronic conditions. In recent years, it has been found that macromolecular polysaccharide has a significant effect on T2DM, various polysaccharides such as Angelica Sinensis Polysaccharide (ASP), Poriacocos polysaccharide and Atractylodesmacrocephala polysaccharide in DSS have effects on T2DM, but mechanism of polysaccharides of DSS(p-DSS) at the metabolic level is still unclear. The purpose of this work is to study the male and female mechanisms of p-DSS in treating T2DM based on metabolomics. Materials and Methods: In this study, metabolomics was used to elucidate the therapeutic mechanism of DSS in T2DM. Urinary samples were collected from male and female rats with T2DM, induced by a high-sugar and high-fat diet combined with Streptozotocin (STZ), to measure the levels of biochemical markers. Urinary metabolomics-based analysis using ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS) was conducted to evaluate the differential metabolites from multiple metabolic pathways. Results: After treatment with p-DSS for 4 weeks, biochemical indicators, including Fasting Blood Glucose (FBG), Fasting Insulin (FINS), Oral Glucose Tolerance Test (OGTT), Insulin Tolerance Test (ITT) and Homeostasis Model Assessment of Insulin Resistance (HOMA-IR), were significantly improved. Metabolomics results revealed that p-DSS regulated the biomarkers, such as PC, 2-oxoglutarate, NAAG in TCA cycle and alanine, aspartate and glutamate metabolism for male rats, on the contrary, leukotriene B4, cholic acid in arachidonic acid metabolism and primary bile acid biosynthesis for female rats. Conclusions: Based on metabolomics, the mechanisms of p- DSS in male and female rats are not identical.
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基于uplc - qtof - ms的代谢组学研究揭示当归少药散多糖对2型糖尿病大鼠的作用
背景:2型糖尿病(T2DM)是目前全球最突出的慢性疾病之一。近年来研究发现大分子多糖对T2DM有显著影响,DSS中多种多糖如当归多糖(ASP)、茯苓多糖、苍术多糖等均对T2DM有影响,但DSS多糖(p-DSS)在代谢水平的作用机制尚不清楚。本研究的目的是基于代谢组学研究p-DSS治疗T2DM的男女机制。材料与方法:本研究采用代谢组学方法阐明DSS治疗T2DM的机制。采用高糖高脂饮食联合链脲佐菌素(STZ)诱导的T2DM大鼠,采集其尿液样本,测定其生化指标水平。采用超高效液相色谱联用四极杆飞行时间质谱(UPLC-Q-TOF-MS)对尿代谢组学进行分析,以评估多种代谢途径的差异代谢物。结果:p-DSS治疗4周后,患者空腹血糖(FBG)、空腹胰岛素(FINS)、口服葡萄糖耐量试验(OGTT)、胰岛素耐量试验(ITT)、胰岛素抵抗稳态模型评估(HOMA-IR)等生化指标均有明显改善。代谢组学结果显示,p-DSS调节雄性大鼠TCA循环中的PC、2-氧葡萄糖酸酯、NAAG以及丙氨酸、天冬氨酸和谷氨酸代谢,而雌性大鼠花生四烯酸代谢和初级胆汁酸生物合成中的白三烯B4、胆酸。结论:基于代谢组学,p- DSS在雄性和雌性大鼠中的作用机制并不相同。
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