• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一种胰高血糖素样肽-1受体激动剂通过调节肠道微生物群结构降低体重。

A Glucagon-Like Peptide-1 Receptor Agonist Lowers Weight by Modulating the Structure of Gut Microbiota.

作者信息

Zhao Li, Chen Yi, Xia Fangzhen, Abudukerimu Buatikamu, Zhang Wen, Guo Yuyu, Wang Ningjian, Lu Yingli

机构信息

Institute and Department of Endocrinology and Metabolism, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, China.

出版信息

Front Endocrinol (Lausanne). 2018 May 17;9:233. doi: 10.3389/fendo.2018.00233. eCollection 2018.

DOI:10.3389/fendo.2018.00233
PMID:29867765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5966539/
Abstract

In addition to improving glucose metabolism, liraglutide, a glucagon-like peptide-1 receptor agonist, has weight-loss effects. The underlying mechanisms are not completely understood. This study was performed to explore whether liraglutide could lower weight by modulating the composition of the gut microbiota in simple obese and diabetic obese rats. In our study, Wistar and Goto-Kakizaki (GK) rats were randomly treated with liraglutide or normal saline for 12 weeks. The biochemical parameters and metabolic hormones were measured. Hepatic glucose production and lipid metabolism were also assessed with isotope tracers. Changes in gut microbiota were analyzed by 16S rRNA gene sequencing. Both glucose and lipid metabolism were significantly improved by liraglutide. Liraglutide lowered body weight independent of glycemia status. The abundance and diversity of gut microbiota were considerably decreased by liraglutide. Liraglutide also decreased obesity-related microbial phenotypes and increased lean-related phenotypes. In conclusion, liraglutide can prevent weight gain by modulating the gut microbiota composition in both simple obese and diabetic obese subjects.

摘要

除了改善葡萄糖代谢外,胰高血糖素样肽-1受体激动剂利拉鲁肽还具有减肥作用。其潜在机制尚未完全明确。本研究旨在探讨利拉鲁肽是否可通过调节单纯性肥胖和糖尿病肥胖大鼠的肠道微生物群组成来减轻体重。在我们的研究中,将Wistar大鼠和Goto-Kakizaki(GK)大鼠随机给予利拉鲁肽或生理盐水治疗12周。测定生化参数和代谢激素。还用同位素示踪剂评估肝脏葡萄糖生成和脂质代谢。通过16S rRNA基因测序分析肠道微生物群的变化。利拉鲁肽显著改善了葡萄糖和脂质代谢。利拉鲁肽降低体重,且与血糖状态无关。利拉鲁肽使肠道微生物群的丰度和多样性显著降低。利拉鲁肽还减少了与肥胖相关的微生物表型,并增加了与瘦相关的表型。总之,利拉鲁肽可通过调节单纯性肥胖和糖尿病肥胖受试者的肠道微生物群组成来预防体重增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/d02149bdec71/fendo-09-00233-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/1f8a288a3e23/fendo-09-00233-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/8cd90c5e5816/fendo-09-00233-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/063b91b4d86c/fendo-09-00233-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/b05cdf9ec6c2/fendo-09-00233-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/b2bf34180e01/fendo-09-00233-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/7421c8eaa6eb/fendo-09-00233-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/243405e9412c/fendo-09-00233-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/d02149bdec71/fendo-09-00233-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/1f8a288a3e23/fendo-09-00233-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/8cd90c5e5816/fendo-09-00233-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/063b91b4d86c/fendo-09-00233-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/b05cdf9ec6c2/fendo-09-00233-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/b2bf34180e01/fendo-09-00233-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/7421c8eaa6eb/fendo-09-00233-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/243405e9412c/fendo-09-00233-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4f6/5966539/d02149bdec71/fendo-09-00233-g008.jpg

相似文献

1
A Glucagon-Like Peptide-1 Receptor Agonist Lowers Weight by Modulating the Structure of Gut Microbiota.一种胰高血糖素样肽-1受体激动剂通过调节肠道微生物群结构降低体重。
Front Endocrinol (Lausanne). 2018 May 17;9:233. doi: 10.3389/fendo.2018.00233. eCollection 2018.
2
Structural modulation of the gut microbiota and the relationship with body weight: compared evaluation of liraglutide and saxagliptin treatment.肠道微生物组结构的调节及其与体重的关系:利拉鲁肽和沙格列汀治疗的比较评价。
Sci Rep. 2016 Sep 16;6:33251. doi: 10.1038/srep33251.
3
Effects of short chain fatty acid producing bacteria on epigenetic regulation of FFAR3 in type 2 diabetes and obesity.短链脂肪酸产生菌对 2 型糖尿病和肥胖症中 FFAR3 的表观遗传调控的影响。
Gene. 2014 Mar 1;537(1):85-92. doi: 10.1016/j.gene.2013.11.081. Epub 2013 Dec 8.
4
Effect of berberine on hyperglycaemia and gut microbiota composition in type 2 diabetic Goto-Kakizaki rats.小檗碱对 2 型糖尿病 Goto-Kakizaki 大鼠高血糖及肠道微生物组成的影响。
World J Gastroenterol. 2021 Feb 28;27(8):708-724. doi: 10.3748/wjg.v27.i8.708.
5
The key role of a glucagon-like peptide-1 receptor agonist in body fat redistribution.胰高血糖素样肽-1 受体激动剂在体脂再分布中的关键作用。
J Endocrinol. 2019 Feb 1;240(2):271-286. doi: 10.1530/JOE-18-0374.
6
Featured article: Structure moderation of gut microbiota in liraglutide-treated diabetic male rats.特色文章:利拉鲁肽治疗的糖尿病雄性大鼠肠道微生物组结构调节。
Exp Biol Med (Maywood). 2018 Jan;243(1):34-44. doi: 10.1177/1535370217743765. Epub 2017 Nov 24.
7
Gut microbiota mediates positive effects of liraglutide on dyslipidemia in mice fed a high-fat diet.肠道微生物群介导利拉鲁肽对高脂饮食喂养小鼠血脂异常的积极作用。
Front Nutr. 2022 Dec 29;9:1048693. doi: 10.3389/fnut.2022.1048693. eCollection 2022.
8
Effects of Glucagon-Like Peptide-1 Receptor Agonists on Gut Microbiota in Dehydroepiandrosterone-Induced Polycystic Ovary Syndrome Mice: Compared Evaluation of Liraglutide and Semaglutide Intervention.胰高血糖素样肽-1受体激动剂对脱氢表雄酮诱导的多囊卵巢综合征小鼠肠道微生物群的影响:利拉鲁肽和司美格鲁肽干预的比较评估
Diabetes Metab Syndr Obes. 2024 Feb 21;17:865-880. doi: 10.2147/DMSO.S451129. eCollection 2024.
9
Early intervention with liraglutide improves glucose tolerance without affecting islet microcirculation in young Goto-Kakizaki rats.利拉鲁肽早期干预可改善年轻的Goto-Kakizaki大鼠的糖耐量,而不影响其胰岛微循环。
Regul Pept. 2012 Aug 20;177(1-3):92-6. doi: 10.1016/j.regpep.2012.05.091. Epub 2012 May 12.
10
Integrated 16S rRNA Sequencing, Metagenomics, and Metabolomics to Characterize Gut Microbial Composition, Function, and Fecal Metabolic Phenotype in Non-obese Type 2 Diabetic Goto-Kakizaki Rats.整合16S rRNA测序、宏基因组学和代谢组学以表征非肥胖型2型糖尿病Goto-Kakizaki大鼠的肠道微生物组成、功能和粪便代谢表型
Front Microbiol. 2020 Jan 20;10:3141. doi: 10.3389/fmicb.2019.03141. eCollection 2019.

引用本文的文献

1
Impact of a structured food sequence and mobile health monitoring on gestational diabetes outcomes: a clinical trial.结构化食物序列和移动健康监测对妊娠期糖尿病结局的影响:一项临床试验。
Front Nutr. 2025 Jul 28;12:1562240. doi: 10.3389/fnut.2025.1562240. eCollection 2025.
2
GLP-1 receptor agonists in IBD: exploring the crossroads of metabolism and inflammation.IBD中的GLP-1受体激动剂:探索代谢与炎症的交叉点
Front Immunol. 2025 Jul 15;16:1610368. doi: 10.3389/fimmu.2025.1610368. eCollection 2025.
3
Bidirectional Interactions Between the Gut Microbiota and Incretin-Based Therapies.

本文引用的文献

1
A proliferative probiotic Bifidobacterium strain in the gut ameliorates progression of metabolic disorders via microbiota modulation and acetate elevation.肠道中增殖性益生菌双歧杆菌通过调节微生物群落和提高乙酸盐水平来改善代谢紊乱的进展。
Sci Rep. 2017 Mar 2;7:43522. doi: 10.1038/srep43522.
2
Berberine improves glucogenesis and lipid metabolism in nonalcoholic fatty liver disease.黄连素改善非酒精性脂肪性肝病中的糖异生和脂质代谢。
BMC Endocr Disord. 2017 Feb 28;17(1):13. doi: 10.1186/s12902-017-0165-7.
3
Structural modulation of the gut microbiota and the relationship with body weight: compared evaluation of liraglutide and saxagliptin treatment.
肠道微生物群与基于肠促胰岛素的疗法之间的双向相互作用。
Life (Basel). 2025 May 23;15(6):843. doi: 10.3390/life15060843.
4
Dietary switch and intermittent fasting ameliorate the disrupted postprandial short-chain fatty acid response in diet-induced obese mice.饮食转换和间歇性禁食可改善饮食诱导肥胖小鼠餐后短链脂肪酸反应紊乱的状况。
EBioMedicine. 2025 Jul;117:105827. doi: 10.1016/j.ebiom.2025.105827. Epub 2025 Jun 24.
5
Effects of semaglutide on metabolism and gut microbiota in high-fat diet-induced obese mice.司美格鲁肽对高脂饮食诱导的肥胖小鼠代谢和肠道微生物群的影响。
Front Pharmacol. 2025 Jun 2;16:1562896. doi: 10.3389/fphar.2025.1562896. eCollection 2025.
6
Effects of beinaglutide on visceral fat area and gut microbiota in obesity.贝那鲁肽对肥胖患者内脏脂肪面积和肠道微生物群的影响。
Eur J Med Res. 2025 Jun 4;30(1):448. doi: 10.1186/s40001-025-02585-5.
7
Comparing the Efficacy of Liraglutide and Semaglutide on Weight Loss: Experience from the Middle East Gulf Region and Literature Review.比较利拉鲁肽和司美格鲁肽在减肥方面的疗效:来自中东海湾地区的经验及文献综述
Hosp Pharm. 2025 May 21:00185787251340645. doi: 10.1177/00185787251340645.
8
Effects of GLP-1 Analogues and Agonists on the Gut Microbiota: A Systematic Review.胰高血糖素样肽-1类似物和激动剂对肠道微生物群的影响:一项系统评价。
Nutrients. 2025 Apr 9;17(8):1303. doi: 10.3390/nu17081303.
9
Influence of CTG repeats from the human DM1 locus on murine gut microbiota.人类DM1基因座的CTG重复序列对小鼠肠道微生物群的影响。
Comput Struct Biotechnol J. 2025 Feb 19;27:733-743. doi: 10.1016/j.csbj.2025.02.016. eCollection 2025.
10
The Beneficial Effects of GLP-1 Receptor Agonists Other than Their Anti-Diabetic and Anti-Obesity Properties.胰高血糖素样肽-1受体激动剂除抗糖尿病和抗肥胖特性之外的有益作用。
Medicina (Kaunas). 2024 Dec 26;61(1):17. doi: 10.3390/medicina61010017.
肠道微生物组结构的调节及其与体重的关系:利拉鲁肽和沙格列汀治疗的比较评价。
Sci Rep. 2016 Sep 16;6:33251. doi: 10.1038/srep33251.
4
How gut microbes talk to organs: The role of endocrine and nervous routes.肠道微生物如何与器官交流:内分泌和神经途径的作用。
Mol Metab. 2016 May 27;5(9):743-52. doi: 10.1016/j.molmet.2016.05.011. eCollection 2016 Sep.
5
Targeting the gastrointestinal tract to treat type 2 diabetes.针对胃肠道治疗2型糖尿病。
J Endocrinol. 2016 Sep;230(3):R95-R113. doi: 10.1530/JOE-16-0056.
6
Insulin Resistance, Microbiota, and Fat Distribution Changes by a New Model of Vertical Sleeve Gastrectomy in Obese Rats.新型垂直袖状胃切除术对肥胖大鼠胰岛素抵抗、微生物群和脂肪分布变化的影响。
Diabetes. 2016 Oct;65(10):2990-3001. doi: 10.2337/db16-0039. Epub 2016 Jul 18.
7
The bile acid TUDCA increases glucose-induced insulin secretion via the cAMP/PKA pathway in pancreatic beta cells.胆汁酸牛磺熊去氧胆酸(TUDCA)通过环磷酸腺苷/蛋白激酶A(cAMP/PKA)信号通路增加胰腺β细胞中葡萄糖诱导的胰岛素分泌。
Metabolism. 2016 Mar;65(3):54-63. doi: 10.1016/j.metabol.2015.10.021. Epub 2015 Oct 17.
8
Probiotic treatment reduces appetite and glucose level in the zebrafish model.益生菌治疗可降低斑马鱼模型中的食欲和血糖水平。
Sci Rep. 2016 Jan 5;6:18061. doi: 10.1038/srep18061.
9
Type 2 Diabetes Biomarkers of Human Gut Microbiota Selected via Iterative Sure Independent Screening Method.通过迭代式Sure独立筛选法筛选出的人类肠道微生物群的2型糖尿病生物标志物。
PLoS One. 2015 Oct 19;10(10):e0140827. doi: 10.1371/journal.pone.0140827. eCollection 2015.
10
Gut microbiota richness promotes its stability upon increased dietary fibre intake in healthy adults.在健康成年人中,肠道微生物群丰富度会在膳食纤维摄入量增加时促进其稳定性。
Environ Microbiol. 2015 Dec;17(12):4954-64. doi: 10.1111/1462-2920.13006. Epub 2015 Sep 3.