Cited by 1,110Gut microbiota and healthGastrointestinal motility and disordersTryptophan and brain disorders

Breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders

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Kelly, John R., Kennedy, Paul J., Cryan, John F., Dinan, Timothy G., Clarke, Gerard, Hyland, Niall P.·2015·Frontiers in Cellular Neuroscience

Abstract

The emerging links between our gut microbiome and the central nervous system (CNS) are regarded as a paradigm shift in neuroscience with possible implications for not only understanding the pathophysiology of stress-related psychiatric disorders, but also their treatment. Thus the gut microbiome and its influence on host barrier function is positioned to be a critical node within the brain-gut axis. Mounting preclinical evidence broadly suggests that the gut microbiota can modulate brain development, function and behavior by immune, endocrine and neural pathways of the brain-gut-microbiota axis. Detailed mechanistic insights explaining these specific interactions are currently underdeveloped. However, the concept that a "leaky gut" may facilitate communication between the microbiota and these key signaling pathways has gained traction. Deficits in intestinal permeability may underpin the chronic low-grade inflammation observed in disorders such as depression and the gut microbiome plays a critical role in regulating intestinal permeability. In this review we will discuss the possible role played by the gut microbiota in maintaining intestinal barrier function and the CNS consequences when it becomes disrupted. We will draw on both clinical and preclinical evidence to support this concept as well as the key features of the gut microbiota which are necessary for normal intestinal barrier function.

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Crossref · 10.3389/fncel.2015.00392

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  • This communication happens via the gut-brain axis, stress hormones, endocrine, sensory neuronal and neuroimmune pathways, and affects behavioral phenotypes, including stress-related behaviors, anxiety, risk avoidance, and depression.

    “This communication happens via the gut-brain axis, stress hormones, endocrine, sensory neuronal and neuroimmune pathways, and affects behavioral phenotypes, including stress-related behaviors, anxiety, risk avoidance, and depression1–6.”

    From Integrated analysis of behavioral, epigenetic, and gut microbiome analyses in AppNL-G-F, AppNL-F, and wild type mice (2021) · cites this paper as [3]

    The Brain-gut-microbiota axis section describes neural, endocrine and immune signaling, including the stress-response HPA axis, and links microbiota to anxiety and stress-related disorders. The Stress, the gut microbiota and barrier function section also discusses stress-related behaviors and depression. The copy does not establish risk avoidance as an affected behavior, and it presents some of these behavioral links as possible rather than settled. (LLM, conf=0.83)

    Experimental — accuracy not yet measured
  • The gut microbiome can communicate with the CNS and affect neurobiology and behavioral phenotypes.

    “A potential contributor to AD pathology is the gut microbiome as it has been shown that the gut microbiome can communicate with the CNS and affect neurobiology and behavioral phenotypes1–6.”
  • Decreased strength of the intestinal barrier due to dysbiosis permits entry of pathogenic, immune-stimulating, and neuroactive substances into the systemic circulation.

    “Decreased strength of the intestinal barrier due to dysbiosis and other factors permits entry of pathogenic, immune-stimulating, and neuroactive substances into the systemic circulation (Kelly et al., 2015).”

    From Microbiome–microglia connections via the gut–brain axis (2019) · cites this paper as Kelly et al., 2015

  • Gut bacteria and their metabolites can modulate intestinal barrier function.

    “Gut bacteria and their metabolites can modulate intestinal barrier function (Kelly et al., 2015);”

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References 319 · Cited by 1,110

Authors
Kelly, J. R., Kennedy, P. J., Cryan, J. F., Dinan, T. G., Clarke, G., & Hyland, N. P.
Affiliations
University College Cork (IE)
Corresponding author
Clarke, Gerard
Venue
Frontiers in Cellular Neuroscience
Published
2015-10-14
Volume
9
Pages
392-392
ISSN
1662-5102 (ISSN-L)
OpenAlex
W2113842526
Cited by
1,110
References
319
Citations by year
2026: 87 · 2025: 105 · 2024: 111 · 2023: 111 · 2022: 116 · 2021: 151 · 2020: 121 · 2019: 90 · 2018: 88 · 2017: 77 · 2016: 50 · 2015: 1
FWCI
6.98
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Frontiers in Cellular Neuroscience (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
Funders
  • Pfizer
  • Mead Johnson Nutrition
  • National Alliance for Research on Schizophrenia and Depression (20771)
  • Science Foundation Ireland (SFI/12/RC/, 20771, 12/RC/2273, HRA_POR/2011/23, 12/RC/, SFI/12/RC/2273.)
  • APC Microbiome Institute (SFI/12/RC/2273)
  • FP7 Food, Agriculture and Fisheries, Biotechnology (613979)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
  • Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
Keywords
gut microbiota, intestinal permeability, leaky gut, gut-brain axis, stress-related psychiatric disorders, depression, intestinal barrier function, low-grade inflammation, immune pathways, endocrine pathways, neural pathways

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