A compartmental model for simulating the gut-brain axis in gastric function regulation.
Overview
- Department of Chemical and Biomolecular Engineering, Lehigh University, Bethlehem, PA, United States
Abstract
Introduction: Gastric function is regulated by the gut-brain axis, which integrates vagal and enteric nervous system (ENS) pathways. The parasympathetic circuit within the vagal pathway promotes digestion by stimulating peristaltic activity and relaxing the pyloric sphincter (PS) through motor and sensory neurons. In contrast, the sympathetic pathway inhibits digestion by suppressing peristalsis and constricting the PS, highlighting the complex neural coordination involved in gastric regulation.
Methods: We introduce a novel mathematical model of the gut-brain axis using a computationally efficient compartmental modeling framework. The model simulates the vagal and ENS pathways and their corresponding effects on gastric function to enhance our understanding of gut-brain axis regulation. We employ the Michaelis-Menten equation with a Hill coefficient to capture neurotransmitter release at neuromuscular junctions by stimulation of motor neurons and its effects on gastric cells. Motor, or efferent, neurons are modeled for three key stomach regions: the fundus, which exhibits tonic activity; the antrum, which exhibits phasic activity; and the PS, which exhibits both tonic and phasic activity. Thus, the stomach is represented as a three-compartment model. The stomach model extends our previous work by incorporating passive stress and dynamic changes in stomach geometry. Sensory, or afferent, inputs are represented through linear equations that account for chemo- and mechanoreceptor activity, while a binary variable captures the sympathetic response. Afferent and efferent firing rates are linked via fitted curves to effectively close the gut-brain axis feedback loop, borrowing from a similar approach used to model cardiovascular regulation.
Results: The simulation results align with physiological observations, demonstrating inhibitory digestive activity during sympathetic responses and excitatory activity, such as gastric emptying, during parasympathetic responses. During gastric emptying, the interstitial cells of Cajal activity shows constant amplitude for low to medium gastric volumes but exhibits an increase in amplitude at very high gastric volumes. Furthermore, gastric emptying rates decrease with high-calorie liquids due to PS regulation.
Discussion: The flexibility of the model allows for future enhancements based on newly discovered signaling pathways in gut-brain circuitry. The computational efficiency of the model suggests its potential use in developing vagal stimulation therapies for gastrointestinal disorders using closed-loop model-based control.
Reproduced under the paper's license (CC BY), from the paper cited above.
Code
The paper links to its data, not to its authors' code: see the Data section.
The paper's code and data availability statement is in the Data section.
Tracing map
A tracing map links a paper to the code its authors published: this paper has none, so it has no map.
Data
Datasets cited
- github.com/
shanferns/ , at github.com; found in “Data availability statement”gut-brain-axis-compartme nt-model
Data availability statement
The original contributions presented in the study are included in the article/
Reproduced under the paper's license (CC BY), from the paper cited above.
Versions
The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.
Version 2, 28 September 2026
- Authors: added Shannon Q. Fernandes (0009-0007-6186-5162); Mayuresh V. Kothare (0000-0001-7681-7445); removed Shannon Q. Fernandes; Mayuresh V. Kothare
Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, pages, dates, 2 authors, 5 keywords, 2 funders, 120 references.
Cite
This paper
Fernandes, S. Q., & Kothare, M. V. (2026). A compartmental model for simulating the gut-brain axis in gastric function regulation. Frontiers in physiology, 17, 1727491. https://
BibTeX
@article{fernandes2026co
author = {Fernandes, Shannon Q. and Kothare, Mayuresh V.},
title = {{A compartmental model for simulating the gut-brain axis in gastric function regulation}},
journal = {Frontiers in physiology},
year = {2026},
month = jun,
volume = {17},
pages = {1727491},
publisher = {Frontiers Media SA},
issn = {1664-042X},
doi = {10.3389/
url = {https://
pmid = {42318504},
pmcid = {PMC13272412}
}
RIS
TY - JOUR
AU - Fernandes, Shannon Q.
AU - Kothare, Mayuresh V.
TI - A compartmental model for simulating the gut-brain axis in gastric function regulation
T2 - Frontiers in physiology
J2 - Front Physiol
PY - 2026
DA - 2026/
VL - 17
SP - 1727491
SN - 1664-042X
PB - Frontiers Media SA
DO - 10.3389/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.3389/
"type": "article-journal",
"title": "A compartmental model for simulating the gut-brain axis in gastric function regulation",
"container-title": "Frontiers in physiology",
"author": [
{
"family": "Fernandes",
"given": "Shannon Q."
},
{
"family": "Kothare",
"given": "Mayuresh V."
}
],
"container-title-short":
"volume": "17",
"page": "1727491",
"DOI": "10.3389/
"PMID": "42318504",
"PMCID": "PMC13272412",
"ISSN": "1664-042X",
"publisher": "Frontiers Media SA",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
6,
3
]
]
}
}
Similar papers
The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.
- [1] doi:10.1016/j.cpblue.2026.100072 [code]
- NodoMap: A single-cell and spatial transcriptomic atlas of the mouse nodose ganglion.Journal: Cell press blueIn common: 6 references
- [2] doi:10.1016/j.molmet.2026.102371
- A distinct vagus-beta cell neural circuit senses glucose and modulates insulin secretion.Journal: Molecular metabolismIn common: 3 references
- [3] doi:10.1371/journal.pcbi.1013113 [code]
- Systems biology analysis of vasodynamics in mouse cerebral arterioles during resting state and functional hyperemia.Journal: PLoS computational biologyIn common: 2 references
- [4] doi:10.1038/s41467-026-76242-8 [code]
- Whole-brain, all-optical interrogation of neuronal dynamics underlying gut and vascular interoception in zebrafish.Journal: Nature communicationsIn common: 2 references
- [5] doi:10.1038/s41593-026-02321-0 [code]
- Microbial reactivation of host androgens directs enteric neuronal regulation of gut motility.Journal: Nature neuroscienceIn common: 1 reference
- [6] doi:10.1063/5.0308450 [code]
- Computational modeling of human vagus nerve stimulation with three-dimensional fascicular morphology.Journal: APL bioengineeringIn common: 1 reference
- [7] doi:10.1038/s41467-026-75522-7
- High ambient temperature activates a neural circuit for gut glucose uptake in male mice.Journal: Nature communicationsIn common: 1 reference
- [8] doi:10.1016/j.isci.2026.116206 [code]
- Gut distension evokes rapid neural dynamics in vagal and hindbrain populations of larval zebrafish.Journal: iScienceIn common: 1 reference
- [9] doi:10.1038/s41467-026-73896-2 [code]
- The vagus nerve promotes memory in rats via nutrient-induced septo-hippocampal acetylcholine signaling.Journal: Nature communicationsIn common: 1 reference
- [10] doi: [code]
- Going deeper with morphologically detailed neural networks by simulation-based gradient propagationJournal: Frontiers in computational neuroscienceIn common: none (in silico)
Contribute
The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.
Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.
Claim this paper
Correct its record
Say what each link of this record is, remove the ones that are not the paper's, add the ones that are missing. The correction becomes a new version of the record, in its Versions section.
Request its removal
To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).
Discussion, reproductions, activity
Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.
Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.
Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.
