Acarbose reduces Pseudomonas aeruginosa respiratory tract infection in type 2 diabetic mice

Respir Res. 2023 Dec 14;24(1):312. doi: 10.1186/s12931-023-02619-8.

Abstract

Background: Type 2 diabetes mellitus (T2DM) is widely prevalent worldwide, and respiratory tract infections (RTIs) have become the primary cause of death for T2DM patients who develop concurrent infections. Among these, Pseudomonas aeruginosa infection has been found to exhibit a high mortality rate and poor prognosis and is frequently observed in bacterial infections that are concurrent with COVID-19. Studies have suggested that acarbose can be used to treat T2DM and reduce inflammation. Our objective was to explore the effect of acarbose on P. aeruginosa RTI in T2DM individuals and elucidate its underlying mechanism.

Methods: High-fat diet (HFD) induction and P. aeruginosa inhalation were used to establish a RTI model in T2DM mice. The effect and mechanism of acarbose administered by gavage on P. aeruginosa RTI were investigated in T2DM and nondiabetic mice using survival curves, pathological examination, and transcriptomics.

Results: We found that P. aeruginosa RTI was more severe in T2DM mice than in nondiabetic individuals, which could be attributed to the activation of the NF-κB and TREM-1 signaling pathways. When acarbose alleviated P. aeruginosa RTI in T2DM mice, both HIF-1α and NF-κB signaling pathways were inhibited. Furthermore, inhibition of the calcium ion signaling pathway and NF-κB signaling pathway contributed to the attenuation of P. aeruginosa RTI by acarbose in nondiabetic mice.

Conclusions: This study confirmed the attenuating effect of acarbose on P. aeruginosa RTIs in T2DM and nondiabetic mice and investigated its mechanism, providing novel support for its clinical application in related diseases.

Keywords: Acarbose; NF-κB signaling pathway; P. aeruginosa; Respiratory tract infection; Type 2 diabetes mellitus.

MeSH terms

  • Acarbose / pharmacology
  • Acarbose / therapeutic use
  • Animals
  • Diabetes Mellitus, Experimental* / drug therapy
  • Diabetes Mellitus, Type 2* / drug therapy
  • Humans
  • Mice
  • NF-kappa B / metabolism
  • Pseudomonas Infections* / drug therapy
  • Pseudomonas aeruginosa / metabolism
  • Respiratory Tract Infections* / drug therapy

Substances

  • Acarbose
  • NF-kappa B