Evidence map›Paper›PMID 41052299›Full record

ArticleJournal of animal science2025

Comprehensive evaluation of a pea co-product for piglet nutrition: fibre content, protein digestion, and intestinal barrier function.

Maurane Grondin, Messan Kokouvi Djakpa, Frédérique Mayeur-Nickel, Sandra Wiart-Letort, Lucie Le Bot, Frédéric Dessauge, Myriam M-L Grundy

Abstract read
In one paragraph

Article in Journal of animal science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

7 authors.

Maurane GrondinINRAE, UMR1348 PEGASE, Institut Agro, 35590 Saint-Gilles, France.
Messan Kokouvi DjakpaINRAE, UMR1348 PEGASE, Institut Agro, 35590 Saint-Gilles, France.
Frédérique Mayeur-NickelINRAE, UMR1348 PEGASE, Institut Agro, 35590 Saint-Gilles, France.
Sandra Wiart-LetortINRAE, UMR1348 PEGASE, Institut Agro, 35590 Saint-Gilles, France.
Lucie Le BotINRAE, UR1268 BIA, 44316 Nantes, France.
Frédéric DessaugeINRAE, UMR1348 PEGASE, Institut Agro, 35590 Saint-Gilles, France.
Myriam M-L GrundyINRAE, UMR1348 PEGASE, Institut Agro, 35590 Saint-Gilles, France.ORCID 0000-0001-7162-656X

Funding

Brittany Region and MixscienceFrench government grant managed by the Agence Nationale de la Recherche under the France 2030 program ANR-22-EXES-0008INRAE (PHASE division)
6 · The paper itself

Abstract

In pig production, weaning is a critical period associated with digestive intestinal disorders, due to the diet and environmental changes. The incorporation of transitional diets with high fibre and protein content represents a promising nutritional strategy to support piglets during the weaning period. This study examined the in vitro protein digestion and physicochemical properties of a co-product of interest for piglet at weaning: pea cream. The main objectives were i) to characterise pea cream in detail, focusing on its dietary fibre content, ii) to investigate in vitro the hydrolysis of its proteins, and iii) to examine the effect of pea cream digesta on intestinal barrier function using intestinal porcine epithelial cell lines (IPEC-J2). The composition in polysaccharides and the degradation of the pea cell wall were evaluated using biochemical and biophysical methods. The pea proteins from the pea cream were digested using an in vitro model of digestion simulating the upper gastrointestinal tract of pigs (based on the INFOGEST protocol). The obtained digesta were detoxified and then applied to IPEC-J2 cells. The results showed that pea cream was rich in dietary fibres, mainly insoluble, and contained approximately 4.6% protein (on an as fed-basis - 76.9% moisture). The in vitro protein digestibility of pea cream was high, with a significant release of proteins into the aqueous phase of the digesta earlier on during the digestion process. Microscopy revealed that some proteins remained encapsulated within cell wall fragments even after 6 h of digestion. The exposure of IPEC-J2 cells to detoxified pea cream digesta did not compromise the intestinal barrier integrity, as assessed by the passage of labelled molecules (FD4 and lucifer yellow) and the analysis of tight junction proteins (ZO-1 and occludin). In conclusion, pea cream presents several characteristics that make it a promising candidate for improving piglet weaning. It is a potential source of easily hydrolysable proteins, and its dietary fibres appear to maintain intestinal barrier function in the small intestine.

Indexed as

Animal FeedDietary FiberDietary ProteinsDigestionPisum sativumAnimal Nutritional Physiological PhenomenaAnimalsCell LineDietIntestinal Barrier FunctionIntestinal MucosaSwineDietary FiberDietary Proteinsdietary fibregut barrier functionin vitro protein digestionIPEC-J2paracellular transportPea cream

Identifiers

PMID41052299
PMCPMC12687584

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Registered trials

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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.