Chen Qi, Gao Yuanyuan, Li Fangyu, Yuan Li
Department of Endocrinology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Diabetes Obes Metab. 2025 Apr;27(4):1676-1692. doi: 10.1111/dom.16225. Epub 2025 Feb 6.
The gastrointestinal tract plays a vital role in the occurrence and treatment of metabolic diseases. Recent studies have convincingly demonstrated a bidirectional axis of communication between the gut and islets, enabling the gut to influence glucose metabolism and energy homeostasis in animals strongly. The 'gut-islet axis' is an essential endocrine signal axis that regulates islet function through the dialogue between intestinal microecology and endocrine metabolism. The discovery of glucagon-like peptide-1 (GLP-1), gastric inhibitory peptide (GIP) and other gut hormones has initially set up a bridge between gut and islet cells. However, the influence of other factors remains largely unknown, such as the homeostasis of the gut microbiota and the integrity of the gut barrier. Although gut microbiota primarily resides and affect intestinal function, they also affect extra-intestinal organs by absorbing and transferring metabolites derived from microorganisms. As a result of this transfer, islets may be continuously exposed to gut-derived metabolites and components. Changes in the composition of gut microbiota can damage the intestinal barrier function to varying degrees, resulting in increased intestinal permeability to bacteria and their derivatives. All these changes contribute to the severe disturbance of critical metabolic pathways in peripheral tissues and organs. In this review, we have outlined the different gut-islet axis signalling mechanisms associated with metabolism and summarized the latest progress in the complex signalling molecules of the gut and gut microbiota. In addition, we will discuss the impact of the gut renin-angiotensin system (RAS) on the various components of the gut-islet axis that regulate energy and glucose homeostasis. This work also indicates that therapeutic approaches aiming to restore gut microbial homeostasis, such as probiotics and faecal microbiota transplantation (FMT), have shown great potential in improving treatment outcomes, enhancing patient prognosis and slowing down disease progression. Future research should further uncover the molecular links between the gut-islet axis and the gut microbiota and explore individualized microbial treatment strategies, which will provide an innovative perspective and approach for the diagnosis and treatment of metabolic diseases.
胃肠道在代谢性疾病的发生和治疗中起着至关重要的作用。最近的研究令人信服地证明了肠道与胰岛之间存在双向通讯轴,使肠道能够强烈影响动物的葡萄糖代谢和能量稳态。“肠-胰岛轴”是一条重要的内分泌信号轴,通过肠道微生态与内分泌代谢之间的对话来调节胰岛功能。胰高血糖素样肽-1(GLP-1)、胃抑制肽(GIP)等肠道激素的发现初步在肠道和胰岛细胞之间架起了一座桥梁。然而,其他因素的影响在很大程度上仍不为人知,如肠道微生物群的稳态和肠道屏障的完整性。尽管肠道微生物群主要存在于肠道并影响肠道功能,但它们也通过吸收和转移微生物衍生的代谢产物来影响肠道外器官。由于这种转移,胰岛可能会持续暴露于源自肠道的代谢产物和成分。肠道微生物群组成的变化会不同程度地损害肠道屏障功能,导致肠道对细菌及其衍生物的通透性增加。所有这些变化都会导致外周组织和器官中关键代谢途径的严重紊乱。在这篇综述中,我们概述了与代谢相关的不同肠-胰岛轴信号传导机制,并总结了肠道和肠道微生物群复杂信号分子的最新进展。此外,我们将讨论肠道肾素-血管紧张素系统(RAS)对调节能量和葡萄糖稳态的肠-胰岛轴各个组成部分的影响。这项工作还表明,旨在恢复肠道微生物群稳态的治疗方法,如益生菌和粪便微生物群移植(FMT),在改善治疗效果、提高患者预后和减缓疾病进展方面已显示出巨大潜力。未来的研究应进一步揭示肠-胰岛轴与肠道微生物群之间的分子联系,并探索个性化的微生物治疗策略,这将为代谢性疾病的诊断和治疗提供创新的视角和方法。