The role of gut microbiota in Tirzepatide-mediated alleviation of high-fat diet-induced obesity
- PMID: 40516844
- DOI: 10.1016/j.ejphar.2025.177827
The role of gut microbiota in Tirzepatide-mediated alleviation of high-fat diet-induced obesity
Abstract
Purpose: In this study, we aim to explore the effects of tirzepatide on the gut microbiota in mice with obesity induced by a high-fat diet.
Methods: Forty male C57BL/6J mice, aged six weeks, were randomly assigned to one of four experimental groups: normal control diet, normal control diet with tirzepatide treatment (NCD + TZP), high-fat diet and high-fat diet with tirzepatide treatment (HFD + TZP). Mice in the HFD group were fed a high-fat diet for ten weeks to establish an obesity model. Subsequently, the NCD + TZP and HFD + TZP groups received subcutaneous tirzepatide injections for 14 days, while the NCD and HFD groups were administered an equivalent volume of saline solution.
Results: The results showed that tirzepatide significantly suppressed weight gain, reduced the area under the curve in glucose tolerance tests, improved insulin resistance, and decreased adipose tissue mass in mice. Moreover, tirzepatide effectively attenuated lipid deposition and fat droplet formation in the livers of obese mice while modulating the expression of genes implicated in abnormal glucose metabolism. Regarding gut microbiota, tirzepatide alleviated high-fat diet-induced dysbiosis by altering microbial composition and diversity. Following high-fat diet exposure, the abundance of certain bacterial genera-including Akkermansia, Bacteroides, Mucispirillum, Enterococcus, and Alistipes-significantly declines, whereas Faecalibaculum, Allobaculum, and Ileibacterium exhibit notable increases. Tirzepatide intervention facilitated the restoration of gut microbiota homeostasis after high-fat diet exposure. Additionally, correlation analyses revealed that Akkermansia, Bacteroides, and Enterococcus levels negatively correlate with weight gain, blood glucose levels, and various obesity-related indicators, whereas Ileibacterium and Allobaculum abundance positively associates with obesity-related traits.
Conclusion: In summary, our findings indicate that tirzepatide has the potential to alleviate high-fat diet-induced gut microbiota dysbiosis in mice. Furthermore, changes in the abundance of specific microbial communities linked to obesity-related outcomes may play a role in the anti-obesity effects of tirzepatide.
Keywords: Anti-obesity drugs; Gut microbiota; Obesity; Tirzepatide.
Copyright © 2025 Elsevier B.V. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare that there are no conflicts of interest.
Similar articles
-
Dietary Branched-Chain Amino Acids Restriction in High-Fat Diet-Induced Obese Mice: Effects on Metabolic Homeostasis, Adipose Inflammation, and Gut Microbiota.J Nutr. 2025 Aug;155(8):2700-2710. doi: 10.1016/j.tjnut.2025.05.049. Epub 2025 Jun 20. J Nutr. 2025. PMID: 40545141
-
Semaglutide alleviates gut microbiota dysbiosis induced by a high-fat diet.Eur J Pharmacol. 2024 Apr 15;969:176440. doi: 10.1016/j.ejphar.2024.176440. Epub 2024 Feb 24. Eur J Pharmacol. 2024. PMID: 38402930
-
Beneficial metabolic effects of PAHSAs depend on the gut microbiota in diet-induced obese mice but not in chow-fed mice.Proc Natl Acad Sci U S A. 2024 Jul 9;121(28):e2318691121. doi: 10.1073/pnas.2318691121. Epub 2024 Jul 5. Proc Natl Acad Sci U S A. 2024. PMID: 38968121 Free PMC article.
-
Interaction between dietary omega-3 polyunsaturated fatty acids, obesity and gut microbiota in preclinical models: A systematic review of randomized controlled trials.Diabetes Obes Metab. 2025 Sep;27(9):4643-4661. doi: 10.1111/dom.16535. Epub 2025 Jun 19. Diabetes Obes Metab. 2025. PMID: 40536121 Review.
-
Gut microbiota dysbiosis -associated obesity and its involvement in cardiovascular diseases and type 2 diabetes. A systematic review.Microvasc Res. 2024 Jan;151:104601. doi: 10.1016/j.mvr.2023.104601. Epub 2023 Sep 9. Microvasc Res. 2024. PMID: 37690507
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical