Abstract

Type 2 diabetes mellitus (T2DM) is a chronic metabolic disease. Sophora flavescens (S. flavescens), also named Kushen, is a famous Chinese herbal medicine that has been used to prevent and cure T2DM both in folk medicine and in medical institution. However, its mechanism of action remains unclear. In this study, the pharmacodynamic effects of S. flavescens EtOAc extract (SFE) on high-fat diet and low-dose streptozotocin-induced T2DM rats were examined. Fecal metabolomics analysis and 16S rRNA gene sequencing were applied to determine the influence of T2DM and SFE treatment on gut microbiota and host metabolism. Based on the consistency of the results of metabolic pathways in metabolomics analysis and phylogenetic investigation of communities by reconstruction of unobserved state (PICRUSt) analysis of 16S rRNA gene sequencing, the level of metabolites and the operational taxonomic units of gut bacteria were combined, and Spearman's analysis was implemented. Our data showed that SFE significantly decreased fasted blood glucose levels and improved lipid profile, glycosylated serum protein, glycosylated hemoglobin index, and pancreas damage. Metabolomics and 16S rRNA gene sequencing analysis indicated gut bacteria disorder, disturbed lipid metabolism, carbohydrate metabolism, and especially amino acid metabolism in T2DM and that SFE can regulated these metabolic pathways through the influence on gut bacteria. Spearman's analysis indicated that the amino acid metabolism that included tryptophan, branched chain amino acid, aromatic amino acid, beta-alanine, and glycine, serine and threonine metabolism, lipid metabolism, including lysophosphatidylcholines and lysophosphatidylethanolamines, primary bile acid and linoleic acid metabolism, carbohydrate metabolism, and nucleotide metabolism positively correlated with Faecalibacterium, Flexispira, Phascolarctobacterium, Prevotella, Roseburia, and [Prevotella]. In addition, arginine and proline metabolism, steroid hormone, steroid biosynthesis, and sphingolipid metabolism positively correlated with Lactobacillus, Oscillospira, Parabacteroides, Ruminococcus, and Streptococcus. Taken together, we speculated that SFE may have an effect on T2DM by mediating host-microbial metabolic axis. Exploration of SFE treatment for T2DM by multiomics is expected to provide a reference for clinical treatment.

Highlights

  • Type 2 diabetes mellitus (T2DM) is a dramatic chronic metabolic disease that is characterized by a high blood glucose level and has a high prevalence worldwide [1]

  • The results showed that arginine and proline metabolism, sphingolipid metabolism, steroid hormone biosynthesis, and steroid biosynthesis were positively correlated with Lactobacillus, Oscillospira, Parabacteroides, Coprococcus, Ruminococcus, and Streptococcus and negatively correlated with Bacteroides, Faecalibacterium, Flexispira, Phascolarctobacterium, Prevotella, Roseburia, and [Prevotella]

  • Multiomics was acted as a research tool to determine how T2DM changes gut bacteria and we clarified the interaction between gut bacteria and metabolites. 16S rRNA gene sequencing analysis implied that disturbed composition of gut bacteria may directly aggravate T2DM or indirectly promote the development of T2DM by disturbing amino acids, lipid, energy, carbohydrate, and glycan biosynthesis and metabolism

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Summary

Introduction

Type 2 diabetes mellitus (T2DM) is a dramatic chronic metabolic disease that is characterized by a high blood glucose level and has a high prevalence worldwide [1]. Oxidative stress can lead to the development of diabetes by damaging islet β cells and reducing the sensitivity of peripheral tissues to insulin. Persistent hyperglycemia and oxidative stress can result in multiorgan damage and complications, and T2DM becomes a major threat to human life and health after cardiovascular diseases and cancer [2]. The human intestinal tract is a natural bioreactor for diverse and highly mutualistic microorganisms and accommodates a variety of gut microbiota, which are important for glucose, amino acid, and lipid metabolism [3, 4]. Gut bacteria can directly affect host metabolism through fermentation.

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