Frontiers in Pharmacology (Sep 2022)

Study on the mechanism of American ginseng extract for treating type 2 diabetes mellitus based on metabolomics

  • Tiantian Liu,
  • Dan Wang,
  • Dan Wang,
  • Xinfeng Zhou,
  • Jiayin Song,
  • Zijun Yang,
  • Chang Shi,
  • Rongshan Li,
  • Yanwen Zhang,
  • Jun Zhang,
  • Jiuxing Yan,
  • Xuehui Zhu,
  • Ying Li,
  • Min Gong,
  • Chongzhi Wang,
  • Chunsu Yuan,
  • Yan Cui,
  • Xiaohui Wu

DOI
https://doi.org/10.3389/fphar.2022.960050
Journal volume & issue
Vol. 13

Abstract

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American ginseng extract (AGE) is an efficient and low-toxic adjuvant for type 2 diabetes mellitus (T2DM). However, the metabolic mechanisms of AGE against T2DM remain unknown. In this study, a rat model of T2DM was created and administered for 28 days. Their biological (body weight and serum biochemical indicators) and pathological (pancreatic sections stained with HE) information were collected for further pharmacodynamic evaluation. Moreover, an ultra-performance liquid chromatography–mass spectrometry–based (UHPLC–MS/MS–based) untargeted metabolomics method was used to identify potential biomarkers of serum samples from all rats and related metabolic pathways. The results indicated that body weight, fasting blood glucose (FBG), fasting blood insulin (FINS), blood triglyceride concentration (TG), high-density lipoprotein cholesterol (HDL-C), insulin resistance index (HOMA-IR) and insulin sensitivity index (ISI), and impaired islet cells were significantly improved after the high dose of AGE (H_AGE) and metformin treatment. Metabolomics analysis identified 101 potential biomarkers among which 94 metabolites had an obvious callback. These potential biomarkers were mainly enriched in nine metabolic pathways linked to amino acid metabolism and lipid metabolism. Tryptophan metabolism and glutathione metabolism, as differential metabolic pathways between AGE and metformin for treating T2DM, were further explored. Further analysis of the aforementioned results suggested that the anti-T2DM effect of AGE was closely associated with inflammation, oxidative stress, endothelial dysfunction, dyslipidemia, immune response, insulin resistance, insulin secretion, and T2DM-related complications. This study can provide powerful support for the systematic exploration of the mechanism of AGE against T2DM and a basis for the clinical diagnosis of T2DM.

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