Li Siyu, Xu Kan, Cheng Yi, Chen Lu, Yi Ailin, Xiao Zhifeng, Zhao Xuefei, Chen Minjia, Tian Yuting, Meng Wei, Tang Zongyuan, Zhou Shuhong, Ruan Guangcong, Wei Yanling
Department of Gastroenterology, Chongqing Key Laboratory of Digestive Malignancies, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Basic Medicine College of Army Medical University, Army Medical University, Chongqing, China.
Front Microbiol. 2023 Jun 14;14:1188455. doi: 10.3389/fmicb.2023.1188455. eCollection 2023.
Pharmacological treatment of inflammatory bowel disease (IBD) is inefficient and difficult to discontinue appropriately, and enterobacterial interactions are expected to provide a new target for the treatment of IBD. We collected recent studies on the enterobacterial interactions among the host, enterobacteria, and their metabolite products and discuss potential therapeutic options. Intestinal flora interactions in IBD are affected in the reduced bacterial diversity, impact the immune system and are influenced by multiple factors such as host genetics and diet. Enterobacterial metabolites such as SCFAs, bile acids, and tryptophan also play important roles in enterobacterial interactions, especially in the progression of IBD. Therapeutically, a wide range of sources of probiotics and prebiotics exhibit potential therapeutic benefit in IBD through enterobacterial interactions, and some have gained wide recognition as adjuvant drugs. Different dietary patterns and foods, especially functional foods, are novel therapeutic modalities that distinguish pro-and prebiotics from traditional medications. Combined studies with food science may significantly improve the therapeutic experience of patients with IBD. In this review, we provide a brief overview of the role of enterobacteria and their metabolites in enterobacterial interactions, discuss the advantages and disadvantages of the potential therapeutic options derived from such metabolites, and postulate directions for further research.
炎症性肠病(IBD)的药物治疗效率低下且难以适当停药,肠道细菌相互作用有望为IBD的治疗提供新靶点。我们收集了有关宿主、肠道细菌及其代谢产物之间肠道细菌相互作用的最新研究,并讨论了潜在的治疗选择。IBD中的肠道菌群相互作用受到细菌多样性降低的影响,影响免疫系统,并受宿主遗传学和饮食等多种因素影响。短链脂肪酸、胆汁酸和色氨酸等肠道细菌代谢产物在肠道细菌相互作用中也发挥着重要作用,尤其是在IBD的进展过程中。在治疗方面,多种来源的益生菌和益生元通过肠道细菌相互作用在IBD中显示出潜在的治疗益处,其中一些已作为辅助药物获得广泛认可。不同的饮食模式和食物,特别是功能性食品,是将益生菌和益生元与传统药物区分开来的新型治疗方式。与食品科学的联合研究可能会显著改善IBD患者的治疗体验。在这篇综述中,我们简要概述了肠道细菌及其代谢产物在肠道细菌相互作用中的作用,讨论了由此类代谢产物衍生的潜在治疗选择的优缺点,并提出了进一步研究的方向。