Mouse study in diabetic db/db mice treated with tirzepatide (10 nmol/kg for 8 weeks) demonstrating renoprotective effects with parallel gut microbiota composition changes, identifying specific microbiome alterations associated with improved kidney function, reduced proteinuria, and decreased renal inflammation. Establishes that tirzepatide's diabetic kidney disease benefits involve gut-kidney axis modulation. Provides mechanistic evidence for tirzepatide's gut microbiota-mediated renoprotection in DKD—supporting the emerging paradigm that GLP-1/GIP agonist benefits in chronic kidney disease involve microbiome-dependent pathways beyond direct renal receptor signaling.
Abstract
PURPOSE: This study evaluated the effect of Tirzepatide on metabolic profiles, kidney function, and gut microbiota composition in mice with diabetic kidney disease (DKD) and clarify the relationship between gut microbiota alterations and the renoprotective effects.
METHODS: Seven-week-old diabetic db/db mice and db/m controls were randomly assigned to three groups: db/db, db/db-T, and db/m. In the db/db-T group, mice received 10 nmol/kg Tirzepatide injections for a duration of 8 weeks. Biochemical and histopathological analyses were used to assess body weight, blood glucose, lipid profile, hepatic and renal function, and renal histopathological changes in mice. An antibiotic-pretreated group (ABX-db/db-T) was established to explore the impact of gut microbiome depletion on the therapeutic effects of Tirzepatide.The composition of gut microbiota was determined through 16S rRNA gene sequencing to assess microbial differences among groups.
RESULTS: Tirzepatide notably decreased fasting blood glucose (FBG), food intake, body weight, glycated hemoglobin A1c (HbA1c), blood lipid levels, and liver function markers, while improving renal function in mice. The renoprotective effects of Tirzepatide were attenuated following gut microbiota depletion. Microbiota analysis revealed that Tirzepatide could reverse dysbiosis and reshape the gut microbial ecosystem. Tirzepatide treatment raised the proportion of beneficial genera,andwhile reducing potentially pathogenic genera,and. Moreover, these microbiota changes were significantly correlated with serum creatinine and urinary albumin/creatinine ratio.
CONCLUSION: Tirzepatide improves renal function and metabolic parameters in DKD mice through gut microbiome regulation. The underlying mechanism involves the modulation of gut-renal axis through the optimization of microbial composition, promoting the development of beneficial bacteria while inhibiting harmful microbes. These results establish a foundational understanding for the use of Tirzepatide in DKD and suggest that combined interventions targeting the gut microbiota may have potential clinical value.