丁酸梭菌通过IL-22/Reg3通路恢复小鼠创伤性脑损伤后肠道屏障完整性

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
Journal of neurotrauma Pub Date : 2025-10-01 Epub Date: 2025-08-29 DOI:10.1177/08977151251367404
Min Liu, Ying Pang, Li Xu, Tongjie Ji, Junyu Yang, Dan Huang, Meng Cheng, Mu Chen, Bingsong Huang, Siyi Xu, Kaijun Zhao, Jing Zhang, Takehiko Yokomizo, Chunlong Zhong
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引用次数: 0

摘要

创伤性脑损伤(TBI)破坏肠道屏障,将脑创伤与全身炎症和继发性并发症联系起来。本研究采用皮质冲击小鼠模型,研究了创伤性脑损伤后肠道微生物群及其代谢物在肠道屏障功能障碍中的作用。tbi诱导的肠道生态失调的特征是微生物多样性减少和丁酸产生菌的损失,这导致短链脂肪酸(SCFAs)水平下降,尤其是丁酸。这种破坏破坏了白细胞介素22/再生胰岛衍生蛋白3 (IL-22/Reg3)信号通路,这对于维持肠道屏障的完整性至关重要。补充丁酸梭菌可恢复丁酸产量,增强IL-22/Reg3表达,减轻tbi诱导的肠道通透性。这些发现确定了SCFA/IL-22/Reg3轴是TBI后肠道屏障稳态的关键介质,并强调了丁酸生成益生菌在治疗TBI相关肠道并发症中的潜在治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clostridium butyricum Restores Intestinal Barrier Integrity via the IL-22/Reg3 Pathway Following Traumatic Brain Injury in Mice.

Traumatic brain injury (TBI) disrupts the intestinal barrier, linking brain trauma to systemic inflammation and secondary complications. This study investigated the role of gut microbiota and its metabolites in intestinal barrier dysfunction following TBI, using a controlled cortical impact mouse model. TBI-induced gut dysbiosis was characterized by reduced microbial diversity and a loss of butyrate-producing bacteria, which led to decreased levels of short-chain fatty acids (SCFAs), particularly butyric acid. This disruption compromised the interleukin-22/regenerating islet-derived protein 3 (IL-22/Reg3) signaling pathway, which is essential for maintaining gut barrier integrity. Supplementation with Clostridium butyricum restored butyric acid production, enhanced IL-22/Reg3 expression, and alleviated TBI-induced intestinal permeability. These findings identify the SCFA/IL-22/Reg3 axis as a key mediator of gut barrier homeostasis after TBI and highlight the potential therapeutic role of butyrate-producing probiotics in managing TBI-associated intestinal complications.

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来源期刊
Journal of neurotrauma
Journal of neurotrauma 医学-临床神经学
CiteScore
9.20
自引率
7.10%
发文量
233
审稿时长
3 months
期刊介绍: Journal of Neurotrauma is the flagship, peer-reviewed publication for reporting on the latest advances in both the clinical and laboratory investigation of traumatic brain and spinal cord injury. The Journal focuses on the basic pathobiology of injury to the central nervous system, while considering preclinical and clinical trials targeted at improving both the early management and long-term care and recovery of traumatically injured patients. This is the essential journal publishing cutting-edge basic and translational research in traumatically injured human and animal studies, with emphasis on neurodegenerative disease research linked to CNS trauma.
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