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肠道菌群和胆汁酸通过TGR5/TRPV1信号通路在糖尿病性周围神经病理性疼痛中的潜在作用机制

The potential mechanism of action of gut flora and bile acids through the TGR5/TRPV1 signaling pathway in diabetic peripheral neuropathic pain.

作者信息

Chen Peng, Jiang Xian, Fu Jia, Ou Cehua, Li Yao, Jia Jing, Liao Changli

机构信息

Department of Pediatrics, Southwest Medical University, Luzhou, Sichuan, China.

Department of Anesthesiology, Luzhou People's Hospital, Luzhou, Sichuan, China.

出版信息

Front Endocrinol (Lausanne). 2024 Nov 15;15:1419160. doi: 10.3389/fendo.2024.1419160. eCollection 2024.

Abstract

Diabetic peripheral neuropathic pain (DPNP) is a major complication of diabetes that markedly affects the quality of life and health status of patients. Recent studies have investigated the potential regulatory influence of gut flora and bile acids on DPNP via the TGR5/TRPV1 signaling pathway. Dysbiosis of the gut flora not only directly affects bile acid metabolism but also significantly correlates with diabetes-associated neuropathy through interactions with the bile acid receptor TGR5 and the ion channel TRPV1. This review describes how alterations in the gut flora and bile acid metabolism contribute to the pathogenesis of DPNP through the TGR5/TRPV1 signaling pathway, revealing potential applications for this pathway in DPNP management. Furthermore, experimental and clinical studies have demonstrated the modulation of gut flora and bile acid metabolism as well as targeting the TGR5/TRPV1 signaling pathway as an innovative therapeutic approach. Further studies are warranted to elucidate the underlying mechanism and develop treatment modalities based on gut flora regulation and signaling pathway interventions, thus providing novel insights and approaches for DPNP therapy.

摘要

糖尿病性周围神经病理性疼痛(DPNP)是糖尿病的一种主要并发症,显著影响患者的生活质量和健康状况。最近的研究探讨了肠道菌群和胆汁酸通过TGR5/TRPV1信号通路对DPNP的潜在调节作用。肠道菌群失调不仅直接影响胆汁酸代谢,还通过与胆汁酸受体TGR5和离子通道TRPV1相互作用,与糖尿病相关神经病变显著相关。本综述描述了肠道菌群和胆汁酸代谢的改变如何通过TGR5/TRPV1信号通路促成DPNP的发病机制,揭示了该信号通路在DPNP管理中的潜在应用。此外,实验和临床研究已证明调节肠道菌群和胆汁酸代谢以及靶向TGR5/TRPV1信号通路是一种创新的治疗方法。有必要进一步研究以阐明其潜在机制,并基于肠道菌群调节和信号通路干预开发治疗方式,从而为DPNP治疗提供新的见解和方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d21/11604420/b51a2a58f2ec/fendo-15-1419160-g001.jpg

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