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Dapagliflozin Modulates the Fecal Microbiota in a Type 2 Diabetic Rat Model. | LitMetric

Dapagliflozin Modulates the Fecal Microbiota in a Type 2 Diabetic Rat Model.

Front Endocrinol (Lausanne)

Department of Endocrinology and Metabolism, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

Published: May 2021

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. Four-week-old male Sprague Dawley rats ( = 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 ( = 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. Dapagliflozin significantly decreased fasting and postprandial blood glucose levels as metformin in type 2 diabetic rats ( < 0.001). Enterotype was composed of after treatment of dapagliflozin, whereas and were the main enterotypes following metformin treatment. Dapagliflozin did not increase the abundance of beneficial bacteria including and . However, these were increased in the metformin group. It is surprising to find that (especially ) were enriched in the dapagliflozin group. 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7707060PMC
http://dx.doi.org/10.3389/fendo.2020.00635DOI Listing

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