Gut-Spinal Cord Axis in Spinal Cord Injury: Bidirectional Inflammatory Mechanisms and Microbiota-Targeted Therapeutic Strategies.

IF 4.1 2区 医学 Q2 IMMUNOLOGY
Journal of Inflammation Research Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S543912
Jinwang Dong, Tao Xie, Cunhu Shi, Gaoqi Feng, Hengheng Zhang, Zhengwei Xu, Liang Dong
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引用次数: 0

Abstract

Spinal cord injury (SCI) is a complex neurological disorder characterized not only by localized neuroinflammation but also by systemic immune dysregulation and multiorgan dysfunction. Emerging evidence has identified the gut microbiota as a critical extrinsic regulator of neural homeostasis, giving rise to the concept of the "gut-spinal cord axis". This review systematically examines the dynamic and bidirectional alterations in the gut microbial composition following SCI, with a particular emphasis on the role of microbiota-derived metabolites in the gut-spinal cord axis. These metabolites are recognized as key mediators that shape the spinal inflammatory milieu by modulating specific signaling pathways. In addition, the mechanistic basis of the gut-spinal cord axis is further dissected through neural, immune, and metabolic regulatory frameworks, highlighting how gut dysbiosis following SCI contributes to spinal inflammation via the modulation of vagal nerve signaling, immune cell polarization, and metabolic homeostasis. Moreover, the translational potential of microbiota-targeted interventions-such as probiotics and fecal microbiota transplantation (FMT)-is evaluated in terms of their ability to suppress inflammatory amplification and restore the disrupted bidirectional gut-spinal cord feedback loop. By integrating multiomics approaches and adopting a spatiotemporal perspective, this review underscores the importance of cross-system therapeutic strategies in SCI, aiming to provide a theoretical foundation and practical guidance for future precision interventions and translational research.

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脊髓损伤中的肠-脊髓轴:双向炎症机制和微生物群靶向治疗策略。
脊髓损伤是一种复杂的神经系统疾病,不仅表现为局部神经炎症,还表现为全身免疫失调和多器官功能障碍。新出现的证据已经确定肠道微生物群是神经稳态的关键外部调节剂,从而产生了“肠-脊髓轴”的概念。这篇综述系统地研究了脊髓损伤后肠道微生物组成的动态和双向变化,特别强调了微生物衍生代谢物在肠-脊髓轴中的作用。这些代谢物被认为是通过调节特定的信号通路来塑造脊柱炎症环境的关键介质。此外,通过神经、免疫和代谢调节框架进一步剖析了肠-脊髓轴的机制基础,强调了脊髓损伤后肠道生态失调如何通过迷走神经信号、免疫细胞极化和代谢稳态的调节导致脊髓炎症。此外,针对微生物群的干预措施(如益生菌和粪便微生物群移植(FMT))的转化潜力是根据它们抑制炎症放大和恢复被破坏的双向肠-脊髓反馈回路的能力来评估的。本文通过整合多组学方法,从时空视角出发,强调跨系统治疗策略在脊髓损伤中的重要性,旨在为未来的精准干预和转化研究提供理论基础和实践指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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