Evidence map›Paper›PMID 42810080›Full record

ArticlePoultry science2026

Characterization and postprandial regulation of the nutrient-sensing machinery in the oral floor mucosa of 10-week-old mule ducks.

Marie Lasserre, Yan Fericelli, Cécile Heraud, Laura-Lou Zwick, Karel Sasso, Sandra Biasutti, Anne Surget, Joelle Dupont, Marianne Houssier, Stéphane Panserat and 2 more

Abstract read
In one paragraph

Article in Poultry science, 2026. 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

12 authors.

Marie LasserreUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Mont-de-Marsan, France.
Yan FericelliUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Mont-de-Marsan, France.
Cécile HeraudUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Saint-Pée-sur-Nivelle, France.
Laura-Lou ZwickUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Mont-de-Marsan, France.
Karel SassoUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Mont-de-Marsan, France.
Sandra BiasuttiUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Mont-de-Marsan, France.
Anne SurgetUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Saint-Pée-sur-Nivelle, France.
Joelle DupontUniversité de Tours, INRAE, CNRS, UMR 7247 PRC, Nouzilly, France.
Marianne HoussierUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Mont-de-Marsan, France.
Stéphane PanseratUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Saint-Pée-sur-Nivelle, France.
Jérôme RoyUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Saint-Pée-sur-Nivelle, France.
Karine GontierUniversité de Pau et des Pays de l'Adour, INRAE, NUMEA, Mont-de-Marsan, France. Electronic address: karine.gontier@univ-pau.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In birds, oral nutrient detection contributes to regulating ingestive behavior, yet the molecular repertoire and postprandial dynamics of gustatory pathways remain poorly defined in ten-week-old ducks. This study evaluated the postprandial responses of nutrient-sensing receptors, calcium-signaling components, and monoaminergic pathways in the oral floor mucosa and central neural tissue of ten-week-old mule ducks. Fed and fasted ducks were sampled at 0 min, 20 min, 2 h, 6 h, and 12 h following meal distribution. Transcriptional profiling revealed a broad chemosensory repertoire spanning sweet, umami, bitter, sour, and fatty acid modalities in the oral floor mucosa, supporting its role as a key sensory interface. However, most gustatory and calcium-signaling genes exhibited remarkable transcriptional stability postprandially at this developmental stage. Notably, only the lipid sensor CD36 (Cluster of differentiation 36) and the bitter receptor T2R116 (Taste receptor type 2 member 116) displayed a significant time × feeding interaction, indicating targeted peripheral responsiveness for fat and bitter perception. Conversely, postprandial changes were marked in monoaminergic circuits. Serotonin metabolism in the oral floor mucosa varied by nutritional state during the early postprandial phase, while elevated central serotonin concentrations and enhanced dopaminergic turnover in fed ducks evidenced acute activation of central satiety and reward circuits. Concurrently, hypothalamic gene expression revealed a synchronized time-dependent downregulation of POMC (Proopiomelanocortin) and MC4R (Melanocortin 4 receptor) up to 6 h post-feeding. In parallel, plasma chemerin levels increased postprandially, highlighting a coordinated peripheral metabolic response. Overall, these results indicate that short-term postprandial regulation in ten-week-old ducks relies predominantly on rapid neurochemical adjustments rather than transcriptional remodeling of peripheral gustatory receptors.

Indexed as

Avian chemosensationHypothalamusNeurotransmitters turnoverOral floor mucosaPostprandial response

Identifiers

PMID42810080
PMCPMC13653973

What OpenQuestion holds

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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.