Evidence map›Paper›PMID 40626374›Full record

ArticleNeurogastroenterology and motility2025

Sex-Dependent Circadian Rhythm Impact on Murine Gastrointestinal Transit.

Shreya S Bellampalli, Gennadiy Fonar, Michael Grynyshyn, Arnaldo Mercado-Perez, Karan H Muchhala, Gianrico Farrugia, Aleksey V Matveyenko, David R Linden, Arthur Beyder

Abstract read
In one paragraph

Article in Neurogastroenterology and motility, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Circadian regulation of gastrointestinal motility and the effect on disorders of gut-brain interaction.Journal of smooth muscle research = Nihon Heikatsukin Gakkai kikanshi · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Shreya S BellampalliDivision of Gastroenterology and Hepatology, Enteric NeuroScience Program (ENSP), Mayo Clinic, Rochester, Minnesota, USA.
Gennadiy FonarDivision of Gastroenterology and Hepatology, Enteric NeuroScience Program (ENSP), Mayo Clinic, Rochester, Minnesota, USA.
Michael GrynyshynDivision of Gastroenterology and Hepatology, Enteric NeuroScience Program (ENSP), Mayo Clinic, Rochester, Minnesota, USA.
Arnaldo Mercado-PerezDivision of Gastroenterology and Hepatology, Enteric NeuroScience Program (ENSP), Mayo Clinic, Rochester, Minnesota, USA.
Karan H MuchhalaDivision of Gastroenterology and Hepatology, Enteric NeuroScience Program (ENSP), Mayo Clinic, Rochester, Minnesota, USA.
Gianrico FarrugiaDivision of Gastroenterology and Hepatology, Enteric NeuroScience Program (ENSP), Mayo Clinic, Rochester, Minnesota, USA.
Aleksey V MatveyenkoDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, Minnesota, USA.
David R LindenDivision of Gastroenterology and Hepatology, Enteric NeuroScience Program (ENSP), Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0002-1727-0387
Arthur BeyderDivision of Gastroenterology and Hepatology, Enteric NeuroScience Program (ENSP), Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0002-9225-4854

Funding

MECHANOTRANSDUCTION IN INTESTINAL SMOOTH MUSCLE CELLSR01DK052766 · NIDDK · MAYO CLINIC ROCHESTER · PI BEYDER, ARTHUR, FARRUGIA, GIANRICO · 1997 to 2025
$8.3M
MSTP at Mayo Clinic RochesterT32GM145408 · NIGMS · MAYO CLINIC ROCHESTER · PI SCOTT H KAUFMANN, LISA A SCHIMMENTI · 2023 to 2026
$4.7M
Mechanotransduction in gastrointestinal physiologyR01DK123549 · NIDDK · MAYO CLINIC ROCHESTER · PI Arthur Beyder · 2019 to 2026
$3.7M
Does the gut have a sense of touch?DP2AT010875 · NCCIH · MAYO CLINIC ROCHESTER · PI BEYDER, ARTHUR · 2019 to 2019
$2.4M
Role of cytoskeletal interactions with mechanogated ion channel Piezo2 in the mechanism of mechanotransduction by enteroendocrine cellsF30DK128913 · NIDDK · MAYO CLINIC ROCHESTER · PI MERCADO-PEREZ, ARNALDO · 2021 to 2025
$229k
Mechanisms of osmosensing in GI enteroendocrine cellsF30DK138638 · NIDDK · MAYO CLINIC ROCHESTER · PI Shreya Bellampalli · 2024 to 2026
$149k
NCCIH NIH HHS DP2 AT010875NIDDK NIH HHS F30 DK128913NIDDK NIH HHS F30 DK138638NIDDK NIH HHS R01 DK052766NIDDK NIH HHS R01 DK123549NIGMS NIH HHS T32 GM145408NIH HHS
6 · The paper itself

Abstract

backgroundThe circadian rhythm regulates gastrointestinal motility. In humans and preclinical models, such as rodents, whole gut transit (WGT) is slower during the rest phase compared to the active phase. Investigators typically study GI transit in rodents during the day, which is their rest phase, rather than during the night, which is their active phase. A circadian rhythm reversal in which mice are in a dark room during the working day (reverse light) allows studies on nocturnal animals during their active phase and has been previously shown to reduce WGT time. GI motility is often disrupted in individuals with disorders of gut-brain interaction (DGBI), which are female predominant. However, the effect of circadian rhythm on regional transit and sex dependence of the differences is not known, as most motility studies looking at circadian rhythm reversal are done in male mice.

methodsWe tested C57BL/6 wild-type male and female mice in rest (12 h of light during the day) and active (reverse cycle for 2 weeks: 12 h of dark during the day) phases. We noted female estrous cycle by visual inspection. We performed carmine WGT by monitoring time-lapse videos of pellet production. We performed fluorescence imaging of excised intestines 30 min after gavage to assess percent fluorescence for each GI region and then examined small intestinal transit (SIT) by measuring geometric center and leading edge. For colonic transit, we monitored bead expulsion time from distal colon to anus. KEY

resultsCompared to rest phase, in the active phase, like male mice, female mice had (1) faster WGT, (2) increased frequency of pellet expulsion in the first 3 h of transit, (3) and greater total pellet production. Both male and female mice in their active phase exhibited (4) more contrast emptied from the stomach and they had (5) further leading edge of fluorescence and (6) geometric center, in SIT, and (7) faster colonic bead expulsion times. There were no significant sex differences in the active phase of WGT. In SIT, male mice had further leading edge in the rest phase than female mice, but this difference was not seen in the active phase, and in colonic transit, male mice in both the active and rest phases had faster bead expulsion than female mice.

conclusionsMice in the active phase have faster regional transit in small and large bowel than mice in the rest phase that collectively contributes to faster WGT times in the active phase of both male and female mice. These findings highlight the importance of circadian biology in sex-dependent rodent GI transit.

Indexed as

Circadian RhythmGastrointestinal TransitSex CharacteristicsAnimalsFemaleMaleMiceMice, Inbred C57BLRestcircadian rhythmcolonsex‐dependencesmall intestinetransit

Identifiers

PMID40626374
PMCPMC12266647

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.