Brain–gut connections in functional GI disorders: Anatomic and physiologic relationships
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Abstract Understanding the neural regulation of gut function and sensation makes it easier to understand the interrelatedness of emotionality, symptom‐attentive behavior or hypervigilance, gut function and pain. The gut and the brain are highly integrated and communicate in a bidirectional fashion largely through the ANS and HPA axis. Within the CNS, the locus of gut control is chiefly within the limbic system, a region of the mammalian brain responsible for both the internal and external homeostasis of the organism. The limbic system also plays a central role in emotionality, which is a nonverbal system that facilitates survival and threat avoidance, social interaction and learning. The generation of emotion and associated physiologic changes are the work of the limbic system and, from a neuroanatomic perspective, the ‘mind‐body interaction’ may largely arise in this region. Finally, the limbic system is also involved in the ‘top down’ modulation of visceral pain transmission as well as visceral perception. A better understanding of the interactions of the CNS, ENS and enteric immune system will significantly improve our understanding of ‘functional’ disorders and allow for a more pathophysiologic definition of categories of patients currently lumped under the broad umbrella of FGID.
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Abnormal HPA signaling causes visceral hypersensitivity, motility changes, and gut barrier dysfunction, contributing to functional GI disorders like IBS.
“Jones et al. (2006) showed that abnormal HPA signaling causes visceral hypersensitivity, motility changes, and gut barrier dysfunction, contributing to functional GI disorders like IBS [64].”
From Chronic Stress and Autoimmunity: The Role of HPA Axis and Cortisol Dysregulation (2025) · cites this paper as [64]
The HPA-axis section (page not available) reports altered HPA signaling in functional GI disorders and says CRH affects gut motility and sensitivity, but it explicitly leaves open whether HPA changes are a cause or a response to symptoms and stressors. The Gut lumen section (page not available) discusses altered permeability in some patients with postinfectious IBS and its possible modulation by autonomic responses; it does not establish that abnormal HPA signaling causes gut barrier dysfunction. (LLM, conf=0.88)
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References 98 · Cited by 358
- Authors
- Jones, M. P., Dilley, J. B., Drossman, D., & Crowell, M. D.
- Affiliations
- Northwestern University (US)
- University of North Carolina at Chapel Hill (US)
- Mayo Clinic (US)
- Corresponding author
- Jones, M. P.
- Venue
- Neurogastroenterology & Motility
- Publisher
- Wiley
- Published
- 2006-01-17
- Volume
- 18
- Issue
- 2
- Pages
- 91-103
- ISSN
- 1350-1925 (ISSN-L)
- 1365-2982
- OpenAlex
- W2034563015
- Cited by
- 358
- References
- 98
- Citations by year
- 2026: 4 · 2025: 15 · 2024: 13 · 2023: 25 · 2022: 20 · 2021: 18 · 2020: 15 · 2019: 19 · 2018: 26 · 2017: 14 · 2016: 24 · 2015: 15 · 2014: 17 · 2013: 16 · 2012: 16
- FWCI
- 1.78
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Neurogastroenterology & Motility (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Health Sciences › Medicine › Psychiatry and Mental health › Psychosomatic Disorders and Their Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Keywords
- gut-brain axis, functional gastrointestinal disorders, limbic system, autonomic nervous system, hypothalamic-pituitary-adrenal axis, visceral pain, visceral sensation, emotionality, enteric nervous system
- MeSH terms
- Animals, Brain, Gastrointestinal Diseases, Humans, Intestines, Pain
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