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糖尿病中的肠-肝轴:机制与治疗机遇

Gut-liver axis in diabetes: Mechanisms and therapeutic opportunities.

作者信息

Abdalla Mona Mohamed Ibrahim

机构信息

Department of Human Biology, School of Medicine, International Medical University, Bukit Jalil 57000, Kuala Lumpur, Malaysia.

出版信息

World J Gastroenterol. 2025 Aug 7;31(29):109090. doi: 10.3748/wjg.v31.i29.109090.


DOI:10.3748/wjg.v31.i29.109090
PMID:40809928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12344363/
Abstract

The gut-liver axis represents a complex, bidirectional communication network between the gastrointestinal tract and the liver, playing a central role in maintaining metabolic homeostasis. In diabetes, disruption of this axis, mediated by gut microbiota dysbiosis, impaired intestinal barrier function, and pro-inflammatory signaling, contributes significantly to insulin resistance, hepatic steatosis, and systemic metabolic dysfunction. This review explores the underlying mechanisms by which microbial alterations, increased gut permeability, and inflammatory pathways influence hepatic insulin resistance and glucose metabolism. In addition to established mechanisms, emerging pathways involving neuroendocrine circuits, microbial metabolites, and immune mediators are discussed, offering deeper insight into gut-liver interactions in metabolic disease. The review also outlines therapeutic strategies targeting the gut-liver axis, including microbiota modulation, barrier function enhancement, and anti-inflammatory interventions, emphasizing their potential in advancing diabetes management. A conceptual framework is proposed to integrate these components into a precision medicine approach for metabolic regulation. Key challenges in clinical translation, including patient heterogeneity and the absence of reliable biomarkers to guide treatment decisions are also discussed to inform future research. By linking mechanistic understanding with therapeutic innovation, the review highlights the gut-liver axis as a promising target for personalized diabetes care.

摘要

肠-肝轴代表了胃肠道与肝脏之间复杂的双向通信网络,在维持代谢稳态中发挥核心作用。在糖尿病中,由肠道微生物群失调、肠道屏障功能受损和促炎信号介导的该轴破坏,对胰岛素抵抗、肝脂肪变性和全身代谢功能障碍有显著影响。本综述探讨了微生物改变、肠道通透性增加和炎症途径影响肝脏胰岛素抵抗和葡萄糖代谢的潜在机制。除了既定机制外,还讨论了涉及神经内分泌回路、微生物代谢产物和免疫介质的新途径,从而更深入地了解代谢性疾病中的肠-肝相互作用。该综述还概述了针对肠-肝轴的治疗策略,包括微生物群调节、屏障功能增强和抗炎干预,强调了它们在推进糖尿病管理方面的潜力。提出了一个概念框架,将这些组成部分整合到代谢调节的精准医学方法中。还讨论了临床转化中的关键挑战,包括患者异质性以及缺乏指导治疗决策的可靠生物标志物,以为未来研究提供参考。通过将机制理解与治疗创新联系起来,该综述强调肠-肝轴是个性化糖尿病护理的一个有前景的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/545b01c2c024/wjg-31-29-109090-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/4aa1487f1064/wjg-31-29-109090-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/b409b4cfeab6/wjg-31-29-109090-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/89f84cab4fa2/wjg-31-29-109090-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/c362b524a0f6/wjg-31-29-109090-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/545b01c2c024/wjg-31-29-109090-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/4aa1487f1064/wjg-31-29-109090-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/b409b4cfeab6/wjg-31-29-109090-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/89f84cab4fa2/wjg-31-29-109090-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/c362b524a0f6/wjg-31-29-109090-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a75/12344363/545b01c2c024/wjg-31-29-109090-g005.jpg

相似文献

[1]
Gut-liver axis in diabetes: Mechanisms and therapeutic opportunities.

World J Gastroenterol. 2025-8-7

[2]
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[6]
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[7]
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[8]
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[9]
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[10]
Gut Microbiota and Metabolites: Biomarkers and Therapeutic Targets for Diabetes Mellitus and Its Complications.

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本文引用的文献

[1]
A Cascade of Microbiota-Leaky Gut-Inflammation- Is it a Key Player in Metabolic Disorders?

Curr Obes Rep. 2025-4-10

[2]
Gut microbiota in the development and progression of chronic liver diseases: Gut microbiota-liver axis.

World J Hepatol. 2025-3-27

[3]
Probiotics and Synbiotics: Applications, Benefits, and Mechanisms for the Improvement of Human and Ecological Health.

J Multidiscip Healthc. 2025-3-11

[4]
Extracellular vesicle-mediated bidirectional communication between the liver and other organs: mechanistic exploration and prospects for clinical applications.

J Nanobiotechnology. 2025-3-8

[5]
Gut microbiota-derived imidazole propionate: an emerging target for the prevention and treatment of cardiometabolic diseases.

Front Endocrinol (Lausanne). 2025-2-17

[6]
Neuro-Nutrition and Exercise Synergy: Exploring the Bioengineering of Cognitive Enhancement and Mental Health Optimization.

Bioengineering (Basel). 2025-2-19

[7]
AhR governs lipid metabolism: the role of gut microbiota.

Front Microbiol. 2025-1-29

[8]
Circulating hs-CRP, IL-18, Chemerin, Leptin, and Adiponectin Levels Reflect Cardiometabolic Dysfunction in Adults with Excess Weight.

Int J Mol Sci. 2025-1-29

[9]
The role of gut microbiota and bacterial translocation in the pathogenesis and management of type 2 diabetes mellitus: Mechanisms, impacts, and dietary therapeutic strategies.

Physiol Behav. 2025-5-1

[10]
Intestinal permeability, food antigens and the microbiome: a multifaceted perspective.

Front Allergy. 2025-1-9

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