Abstract
Background: The gut microbiota is recognized as a major modulator of metabolic disorders such as type 2 diabetes. Dapagliflozin, sodium glucose cotransporter 2 inhibitors (SGLT2i), enhances renal glucose excretion, and lowers blood glucose levels. The study aimed to determine the effects of dapagliflozin on fecal microbiota in a type 2 diabetic rat model.Methods: Four-week-old male Sprague Dawley rats (n = 24) were fed a high-fat diet (HFD) for 8 weeks and then given a single dose of STZ injection (30 mg/kg, i.p). They were randomly divided into three groups (n = 8). Each group received intragastric infusion of normal saline (2 ml, 0.9%) or metformin (215.15 mg/kg/day) or dapagliflozin (1 mg/kg/day) for 4 weeks. Blood glucose levels and plasma insulin levels were detected during intragastric glucose tolerance. Fecal samples were collected to access microbiome by 16S ribosomal RNA gene sequencing.Results: Dapagliflozin significantly decreased fasting and postprandial blood glucose levels as metformin in type 2 diabetic rats (P < 0.001). Enterotype was composed of Ruminococcaceae after treatment of dapagliflozin, whereas Ruminococcaceae and Muribaculaceae were the main enterotypes following metformin treatment. Dapagliflozin did not increase the abundance of beneficial bacteria including Lactobacillaceae and Bifidobacteriaceae. However, these were increased in the metformin group. It is surprising to find that Proteobacteria (especially Desulfovibrionaceae) were enriched in the dapagliflozin group.Conclusion: Dapagliflozin and metformin exerted complementary effects on the main beneficial bacteria. A combination of these two drugs might be beneficial to improve the structure of fecal microbiota in the treatment of type 2 diabetes.
Highlights
Type 2 diabetes (T2D) affects nearly 373.5 million individuals worldwide
Rats were considered the model of type 2 diabetes mellitus when they met the following criteria
Fasting blood glucose levels were significantly decreased after metformin and dapagliflozin treatments compared with the control (P < 0.001, respectively), with no statistical differences between metformin and dapagliflozin treatments
Summary
Type 2 diabetes (T2D) affects nearly 373.5 million individuals worldwide. An increasing number of studies have connected the gut microbiome with metabolic diseases such as diabetes and obesity [1]. The composition and richness of intestinal flora are unique and highly variable. It can be modulated by diet, host health, age, ethnicity, genetics, and antidiabetic medication [4]. Metformin is a first-line medication in the treatment of type 2 diabetes, as it increases the abundance of beneficial bacteria [4, 5], and is associated with higher levels of short-chain fatty acids (SCFAs: acetate, propionate, and butyrate) [6]. The gut microbiota is recognized as a major modulator of metabolic disorders such as type 2 diabetes. The study aimed to determine the effects of dapagliflozin on fecal microbiota in a type 2 diabetic rat model
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