Evidence map›Paper›PMID 41306567›Full record

ArticleFrontiers in physiology2025

From wheat bran to equine gut: the

Berit Boshuizen, Maarten Willems, Lorie De Maré, Guilherme Hosotani, Jean Eduardo De Oliveira, Benjamin Horemans, Carmen Vidal Moreno De Vega, Elisabeth-Lidwien J M M Verdegaal, Catherine Delesalle

Abstract read
In one paragraph

Article in Frontiers in physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Berit Boshuizen *Department of Translational Physiology, Infectiology and Public Health, Research Group of Comparative Physiology, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Maarten Willems *Department of Translational Physiology, Infectiology and Public Health, Research Group of Comparative Physiology, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Lorie De MaréDepartment of Translational Physiology, Infectiology and Public Health, Research Group of Comparative Physiology, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Guilherme HosotaniCargill Research and Development Centre Europe, Vilvoorde, Belgium.
Jean Eduardo De OliveiraCargill Research and Development Centre Europe, Vilvoorde, Belgium.
Benjamin HoremansCargill Research and Development Centre Europe, Vilvoorde, Belgium.
Carmen Vidal Moreno De VegaDepartment of Translational Physiology, Infectiology and Public Health, Research Group of Comparative Physiology, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Elisabeth-Lidwien J M M VerdegaalDepartment of Translational Physiology, Infectiology and Public Health, Research Group of Comparative Physiology, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Catherine DelesalleDepartment of Translational Physiology, Infectiology and Public Health, Research Group of Comparative Physiology, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Aleurone, a bioactive wheat bran component, has been shown to modulate host metabolism and gut microbiota, but its effects across different compartments of the equine gastrointestinal (GI) tract remain unclear. In this study, we aimed to characterize aleurone-derived metabolite profiles using an Methods: Three substrates (control feed, aleurone-containing feed, and pure aleurone) were fermented over 72 h, and targeted metabolomics was performed on 38 metabolites. Results: Significant substrate- and compartment-dependent effects were found for 21 metabolites. Aleurone-containing feed increased asparagine and threonine levels while reducing lactic acid, particularly in the cecum. In contrast, control feed showed the highest overall metabolite abundance, suggesting greater microbial accessibility. Time-resolved analyses revealed dynamic production-utilization patterns; isoleucine, for example, displayed a distinct peak-decay pattern in the colon. Carnitine increased over time across compartments, showing local production, especially in the cecum. Artificial intelligence-based classification models achieved >90% accuracy in distinguishing substrate types and revealed ferulic acid and indole acetic acid as key differentiators. Discussion: The findings suggest that aleurone's structural matrix may influence metabolite release and microbial access, highlighting its functional role in modulating fermentation and overall host metabolism. In this study, we demonstrate that aleurone alters microbial fermentation and metabolite output in a time- and compartment-specific manner. These insights enhance our understanding of aleurone as a functional feed component in horses and provide a foundation for future dietary strategies targeting metabolic and gut health.

Indexed as

aleuroneartificial intelligence modelingequine gastrointestinal tractfunctional feedhindgut microbiotametabolismmetabolomicstime-resolved metabolite profiling

Identifiers

PMID41306567
PMCPMC12643889

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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.