文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

肠道-免疫-脑轴:炎症性肠病神经精神发病机制的重要途径

The Gut-Immune-Brain Axis: An Important Route for Neuropsychiatric Morbidity in Inflammatory Bowel Disease.

机构信息

Department of Molecular Neurology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

Department of Stem Cell Biology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

出版信息

Int J Mol Sci. 2022 Sep 21;23(19):11111. doi: 10.3390/ijms231911111.


DOI:10.3390/ijms231911111
PMID:36232412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9570400/
Abstract

Inflammatory bowel disease (IBD) comprises Crohn's disease (CD) and ulcerative colitis (UC) and is associated with neuropsychiatric symptoms like anxiety and depression. Both conditions strongly worsen IBD disease burden. In the present review, we summarize the current understanding of the pathogenesis of depression and anxiety in IBD. We present a stepwise cascade along a gut-immune-brain axis initiated by evasion of chronic intestinal inflammation to pass the epithelial and vascular barrier in the gut and cause systemic inflammation. We then summarize different anatomical transmission routes of gut-derived peripheral inflammation into the central nervous system (CNS) and highlight the current knowledge on neuroinflammatory changes in the CNS of preclinical IBD mouse models with a focus on microglia, the brain-resident macrophages. Subsequently, we discuss how neuroinflammation in IBD can alter neuronal circuitry to trigger symptoms like depression and anxiety. Finally, the role of intestinal microbiota in the gut-immune-brain axis in IBD will be reviewed. A more comprehensive understanding of the interaction between the gastrointestinal tract, the immune system and the CNS accounting for the similarities and differences between UC and CD will pave the path for improved prediction and treatment of neuropsychiatric comorbidities in IBD and other inflammatory diseases.

摘要

炎症性肠病(IBD)包括克罗恩病(CD)和溃疡性结肠炎(UC),并伴有焦虑和抑郁等神经精神症状。这两种疾病都会使 IBD 的疾病负担大大加重。在本综述中,我们总结了目前对 IBD 中抑郁和焦虑发病机制的理解。我们提出了一个沿着肠道-免疫-脑轴的逐步级联反应,由慢性肠道炎症的逃避引发,穿过肠道的上皮和血管屏障,导致全身炎症。然后,我们总结了肠道来源的外周炎症向中枢神经系统(CNS)的不同解剖传播途径,并强调了目前关于临床前 IBD 小鼠模型中 CNS 神经炎症变化的知识,重点是小胶质细胞,即大脑驻留巨噬细胞。随后,我们讨论了 IBD 中的神经炎症如何改变神经元回路,从而引发抑郁和焦虑等症状。最后,将回顾肠道微生物群在 IBD 中肠道-免疫-脑轴中的作用。更全面地了解胃肠道、免疫系统和中枢神经系统之间的相互作用,解释 UC 和 CD 之间的异同,将为改善 IBD 和其他炎症性疾病的神经精神合并症的预测和治疗铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d791/9570400/46a68ff7252b/ijms-23-11111-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d791/9570400/423638106e2a/ijms-23-11111-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d791/9570400/46a68ff7252b/ijms-23-11111-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d791/9570400/423638106e2a/ijms-23-11111-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d791/9570400/46a68ff7252b/ijms-23-11111-g002.jpg

相似文献

[1]
The Gut-Immune-Brain Axis: An Important Route for Neuropsychiatric Morbidity in Inflammatory Bowel Disease.

Int J Mol Sci. 2022-9-21

[2]
The Roles of Inflammation, Nutrient Availability and the Commensal Microbiota in Enteric Pathogen Infection.

Microbiol Spectr. 2015-6

[3]
Two-Sample Mendelian Randomization Analysis Investigates Causal Associations Between Gut Microbial Genera and Inflammatory Bowel Disease, and Specificity Causal Associations in Ulcerative Colitis or Crohn's Disease.

Front Immunol. 2022

[4]
Gut Microbial Metabolite Butyrate and Its Therapeutic Role in Inflammatory Bowel Disease: A Literature Review.

Nutrients. 2023-5-11

[5]
A Review of Inflammatory Bowel Disease: A Model of Microbial, Immune and Neuropsychological Integration.

Public Health Rev. 2021-5-5

[6]
Psychiatric Comorbidities of Inflammatory Bowel Disease: It Is a Matter of Microglia's Gut Feeling.

Cells. 2024-1-17

[7]
Metagenomic analysis of intestinal mucosa revealed a specific eukaryotic gut virome signature in early-diagnosed inflammatory bowel disease.

Gut Microbes. 2018-9-25

[8]
New insights into the interactions between the gut microbiota and the inflammatory response to ulcerative colitis in a mouse model of dextran sodium sulfate and possible mechanisms of action for treatment with PE&AFWE.

Animal Model Exp Med. 2024-4

[9]
A galectin-specific signature in the gut delineates Crohn's disease and ulcerative colitis from other human inflammatory intestinal disorders.

Biofactors. 2016-2-1

[10]
Bi-directionality of Brain-Gut Interactions in Patients With Inflammatory Bowel Disease.

Gastroenterology. 2018-1-31

引用本文的文献

[1]
Advancements in Immunomodulatory Therapies for IBD and Their Interplay With the Gut-Brain Axis: An Updated Review of Current Literature and Beyond.

Health Sci Rep. 2025-8-10

[2]
Impact of gastrointestinal dysbiosis on tryptophan metabolism and neurological cancer progression.

Med Oncol. 2025-8-6

[3]
Bioactive Properties and Phenolic Profile of Bioaccessible and Bioavailable Fractions of Red Radish Microgreens After In Vitro Digestion.

Molecules. 2025-7-15

[4]
Neuroimaging Insights into the Public Health Burden of Neuropsychiatric Disorders: A Systematic Review of Electroencephalography-Based Cognitive Biomarkers.

Medicina (Kaunas). 2025-5-28

[5]
Identification of overlapping genetic loci between inflammatory bowel disease and major depressive disorder.

Eur Arch Psychiatry Clin Neurosci. 2025-6-20

[6]
Absence of Microglial Activation and Maintained Hippocampal Neurogenesis in a Transgenic Mouse Model of Crohn's Disease.

Cells. 2025-6-4

[7]
From gut inflammation to psychiatric comorbidity: mechanisms and therapies for anxiety and depression in inflammatory bowel disease.

J Neuroinflammation. 2025-6-3

[8]
Mechanism of Wuling powder modulating proBDNF/p75NTR/sortilin and BDNF/TrkB pathways in the treatment of ulcerative colitis complicated with depression.

World J Gastroenterol. 2025-2-28

[9]
Dual Role of α-MSH in Colitis Progression: Mediating Neutrophil Differentiation via Bone Marrow.

J Inflamm Res. 2025-2-10

[10]
Milk-derived extracellular vesicles and gut health.

NPJ Sci Food. 2025-1-30

本文引用的文献

[1]
Microbiota-dependent increase in δ-valerobetaine alters neuronal function and is responsible for age-related cognitive decline.

Nat Aging. 2021-12

[2]
Early stress-induced impaired microglial pruning of excitatory synapses on immature CRH-expressing neurons provokes aberrant adult stress responses.

Cell Rep. 2022-3-29

[3]
Immune regulation by fungal strain diversity in inflammatory bowel disease.

Nature. 2022-3

[4]
Colitis-associated microbiota drives changes in behaviour in male mice in the absence of inflammation.

Brain Behav Immun. 2022-5

[5]
Gut microbiota drives age-related oxidative stress and mitochondrial damage in microglia via the metabolite N-carboxymethyllysine.

Nat Neurosci. 2022-3

[6]
IL-33 in the basolateral amygdala integrates neuroinflammation into anxiogenic circuits via modulating BDNF expression.

Brain Behav Immun. 2022-5

[7]
Mucosal fungi promote gut barrier function and social behavior via Type 17 immunity.

Cell. 2022-3-3

[8]
Bacteroides species differentially modulate depression-like behavior via gut-brain metabolic signaling.

Brain Behav Immun. 2022-5

[9]
Edaravone ameliorates depressive and anxiety-like behaviors via Sirt1/Nrf2/HO-1/Gpx4 pathway.

J Neuroinflammation. 2022-2-7

[10]
Sensory representation and detection mechanisms of gut osmolality change.

Nature. 2022-2

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索