Cited by 113Gut microbiota and healthInflammatory Bowel DiseaseGastrointestinal motility and disorders

The DOI matches its Crossref record; 97 of the 97 references it cites were found in a registry or an index.

Bidirectional gut-brain-microbiota axis as a potential link between inflammatory bowel disease and ischemic stroke

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Abstract

Emerging evidence suggests that gut-brain-microbiota axis (GBMAx) may play a pivotal role linking gastrointestinal and neuronal disease. In this review, we summarize the latest advances in studies of GBMAx in inflammatory bowel disease (IBD) and ischemic stroke. A more thorough understanding of the GBMAx could advance our knowledge about the pathophysiology of IBD and ischemic stroke and help to identify novel therapeutic targets via modulation of the GBMAx.

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Registry

Crossref · 10.1186/s12974-018-1382-3

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Figures

Fig. 1 General concept of bidirectional gut-brain-microbiota axis (GBMAx). The brain regulates the gut and its microbiota via neuroanatomic, immunological, and neuroendocrine-HPA axis pathways, communicating via neurotransmitters, neuropeptides, or microbial-derived products effecting gut microbiota. Accordingly, the gut microbiota influences the brain. These two manners form the bidirectional communication and interactions between the gut and brain
Fig. 1 General concept of bidirectional gut-brain-microbiota axis (GBMAx). The brain regulates the gut and its microbiota via neuroanatomic, immunological, and neuroendocrine-HPA axis pathways, communicating via neurotransmitters, neuropeptides, or microbial-derived products effecting gut microbiota. Accordingly, the gut microbiota influences the brain. These two manners form the bidirectional communication and interactions between the gut and brainCC BY · PubMed Central
Fig. 2 Schematic presentation of the bidirectional interaction of GBMAx in the pathogenesis of ischemic stroke and inflammatory bowel disease (IBD). With ischemic stroke, the excitability of the sympathetic nervous system, enteric neuronal loss, gut permeability, and epithelial damage increases, while gut motility decreases. Gut microbial dysbiosis and the intestinal immune response emerge simultaneously. The changes above are modulated by the GBMAx, aggravating ischemic stroke via microbial interleukin (IL)-17-positive T cell-mediated neuroinflammation. Inflammatory bowel disease (IBD) is a key driving factor for psychological disorders and stress, increasing gut permeability, bacterial translocation, and mucosal immune response and modulating the hypothalamic-pituitary axis response through the GBMAx
Fig. 2 Schematic presentation of the bidirectional interaction of GBMAx in the pathogenesis of ischemic stroke and inflammatory bowel disease (IBD). With ischemic stroke, the excitability of the sympathetic nervous system, enteric neuronal loss, gut permeability, and epithelial damage increases, while gut motility decreases. Gut microbial dysbiosis and the intestinal immune response emerge simultaneously. The changes above are modulated by the GBMAx, aggravating ischemic stroke via microbial interleukin (IL)-17-positive T cell-mediated neuroinflammation. Inflammatory bowel disease (IBD) is a key driving factor for psychological disorders and stress, increasing gut permeability, bacterial translocation, and mucosal immune response and modulating the hypothalamic-pituitary axis response through the GBMAxCC BY · PubMed Central

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Metadata

Authors
Zhao, L., Xiong, Q., Stary, C. M., Mahgoub, O. K., Ye, Y., Gu, L., Xiong, X., & Zhu, S.
Affiliations
  • Renmin Hospital of Wuhan University (CN)
  • Stanford Medicine (US)
  • First Affiliated Hospital Zhejiang University (CN)
Corresponding author
  • Xiong, Xiaoxing
  • Zhu, Shengmei
Venue
Journal of Neuroinflammation
Published
2018-12
Volume
15
Issue
1
Pages
339-339
ISSN
1742-2094 (ISSN-L)
OpenAlex
W2904712122
Cited by
113
References
97
Citations by year
2026: 5 · 2025: 11 · 2024: 13 · 2023: 23 · 2022: 23 · 2021: 17 · 2020: 14 · 2019: 7
FWCI
0.93
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroinflammation (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, other-oa)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • National Natural Science Foundation of China (81571147, 81870939)
  • American Heart Association (14FTF19970029)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
  • Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
Keywords
gut-brain-microbiota axis, inflammatory bowel disease, ischemic stroke, gut microbiota, neuroinflammation, two-way communication, therapeutic target
MeSH terms
Gastrointestinal Microbiome, Animals, Brain Ischemia, Humans, Inflammatory Bowel Diseases

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