Faecalibacterium prausnitzii Improves Lipid Metabolism Disorder and Insulin Resistance in Type 2 Diabetic Mice

Br J Biomed Sci. 2023 Mar 21:80:10794. doi: 10.3389/bjbs.2023.10794. eCollection 2023.

Abstract

Purpose: Additional effective therapeutic strategies for Type 2 diabetes (T2D) patients are urgently needed. Gut microbiota plays an important role in T2D development and is a promising treatment strategy for T2D patients. Faecalibacterium prausnitzii (F. prausnitzii) is regarded as one of the most important bacterial indicators for a healthy gut, but the mechanisms of its anti-diabetic properties are still unclear. Methods and Results: The abundance of F. prausnitzii in feces of patients with T2D was detected by using qPCR. The effects of F. prausnitzii on glucose homeostasis, insulin resistance (IR), dyslipidemia, hepatic steatosis and inflammation were investigated in type 2 diabetic (T2D) db/db mice. We also investigated F. prausnitzii in people. Our results showed that the abundance of F. prausnitzii was significantly lower in T2D patients compared to healthy subjects. In T2D mice, we found that F. prausnitzii treatment significantly decreased fasting blood glucose and IR index, indicating improved glucose intolerance as well as IR. Furthermore, based on evaluation of lipid-regulating enzyme activities and proinflammatory cytokine levels, F. prausnitzii was not only able to improve inflammation in both adipose tissue and liver, but also ameliorate hepatic steatosis through inhibiting the activity of hepatic lipogenic enzymes. Conclusion: These results suggested that F. prausnitzii might serve as a therapeutic option for T2D by improved IR, lipid metabolism and inflammation.

Keywords: Faecalibacterium prausnitzii; hepatic steatosis; inflammation; insulin resistance; lipid metabolism; type 2 diabetic.

MeSH terms

  • Animals
  • Diabetes Mellitus, Experimental*
  • Diabetes Mellitus, Type 2*
  • Faecalibacterium prausnitzii / metabolism
  • Fatty Liver*
  • Humans
  • Inflammation
  • Insulin Resistance*
  • Lipid Metabolism
  • Lipid Metabolism Disorders*
  • Mice

Grants and funding

This work was supported by grants from Natural Science Foundation of Guangdong Province, China (2020A1515010597), Dongguan Science and Technology of Social Development Program (2018507150011651, 201950715001208, and 202050715001215), and National Medical Science and Technology Foundation (W2016CWGD05).