The Role of Gut Microbiota in Tirzepatide-Mediated Alleviation of High-Fat Diet-Induced Obesity.

IF 4.2 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Ruonan Wang, Zijing Lin, Mingjie He, Yi Liao, Yunfei Xu, Chengzhi Chen, Xinhao Duan, XueJun Jiang, Jingfu Qiu
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引用次数: 0

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.

肠道微生物群在替西肽介导的高脂肪饮食引起的肥胖缓解中的作用。
目的:在本研究中,我们旨在探讨替西帕肽对高脂肪饮食引起的肥胖小鼠肠道微生物群的影响。方法:选取6周龄雄性C57BL/6J小鼠40只,随机分为正常对照组饮食、正常对照组饮食加替西帕肽(NCD+TZP)、高脂饮食和高脂饮食加替西帕肽(HFD+TZP) 4组。HFD组小鼠喂食高脂肪饮食10周,建立肥胖模型。随后,NCD+TZP组和HFD+TZP组皮下注射替西帕肽14 d, NCD和HFD组皮下注射等量生理盐水。结果:替西帕肽显著抑制小鼠体重增加,减少糖耐量试验曲线下面积,改善胰岛素抵抗,降低脂肪组织质量。此外,替西肽可以有效地减少肥胖小鼠肝脏中的脂质沉积和脂肪滴形成,同时调节与异常糖代谢有关的基因的表达。在肠道菌群方面,替西肽通过改变微生物组成和多样性来缓解高脂肪饮食引起的生态失调。高脂肪饮食暴露后,某些细菌属(包括Akkermansia、Bacteroides、Mucispirillum、Enterococcus和alistitipum)的丰度显著下降,而Faecalibaculum、Allobaculum和回肠杆菌则显著增加。替西帕肽干预有助于高脂肪饮食暴露后肠道微生物群稳态的恢复。此外,相关分析显示,Akkermansia、Bacteroides和Enterococcus水平与体重增加、血糖水平和各种肥胖相关指标呈负相关,而回肠杆菌和Allobaculum丰度与肥胖相关性状呈正相关。结论:综上所述,我们的研究结果表明,替西帕肽有可能缓解小鼠高脂肪饮食引起的肠道菌群失调。此外,与肥胖相关结果相关的特定微生物群落丰度的变化可能在替西肽的抗肥胖作用中发挥作用。
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来源期刊
CiteScore
9.00
自引率
0.00%
发文量
572
审稿时长
34 days
期刊介绍: The European Journal of Pharmacology publishes research papers covering all aspects of experimental pharmacology with focus on the mechanism of action of structurally identified compounds affecting biological systems. The scope includes: Behavioural pharmacology Neuropharmacology and analgesia Cardiovascular pharmacology Pulmonary, gastrointestinal and urogenital pharmacology Endocrine pharmacology Immunopharmacology and inflammation Molecular and cellular pharmacology Regenerative pharmacology Biologicals and biotherapeutics Translational pharmacology Nutriceutical pharmacology.
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