Evidence map›Paper›PMID 39080345›Full record

ArticleNature communications2024

Harnessing intestinal tryptophan catabolism to relieve atherosclerosis in mice.

Mouna Chajadine, Ludivine Laurans, Tobias Radecke, Nirmala Mouttoulingam, Rida Al-Rifai, Emilie Bacquer, Clara Delaroque, Héloïse Rytter, Marius Bredon, Camille Knosp and 13 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
–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

39 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Colonic metabolomic and transcriptomic alterations in a mouse model of metabolic syndrome.American journal of physiology. Gastrointestinal and liver physiology · 2026
    Article
  4. Treatment with saponins fromNutrition research and practice · 2026
    Article
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  15. Functional potential of gut microbiota inFrontiers in microbiology · 2026
    Article
  16. Article
  17. Review
  18. Review
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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

23 authors.

Mouna ChajadineUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.
Ludivine Laurans *Université Paris Cité, Inserm, PARCC, F-75015, Paris, France.
Tobias Radecke *Université Paris Cité, Inserm, PARCC, F-75015, Paris, France.
Nirmala MouttoulingamUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.
Rida Al-RifaiUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.ORCID 0000-0002-6976-0011
Emilie BacquerUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.
Clara DelaroqueMicrobiome-Host interactions, Institut Pasteur, Université Paris Cité, INSERM U1306, Paris, France.
Héloïse RytterMicrobiome-Host interactions, Institut Pasteur, Université Paris Cité, INSERM U1306, Paris, France.
Marius BredonSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, CRSA, AP-HP, Saint Antoine Hospital, Gastroenterology Department, F-75012, Paris, France.
Camille KnospUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.
José VilarUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.ORCID 0000-0002-9136-7726
Coralie FontaineInserm U1297, Institut des Maladies Métaboliques et Cardiovasculaires, Université de Toulouse, BP 84225, 31 432 Toulouse cedex 04, cedex, France.
Nadine SuffeeUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.ORCID 0000-0001-9277-5089
Marie VandestienneUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.ORCID 0000-0002-6947-9852
Bruno EspositoUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.
Julien DairouUniversité Paris cité, CNRS, Laboratoire de Chimie et de Biochimie Pharmacologiques et Toxicologiques, F-75006 Paris, France. 45 rue des Saints Pères, 75006, Paris, France.
Jean Marie LaunayAssistance Publique Hôpitaux de Paris, Service de Biochimie and INSERM U942, Hôpital Lariboisière, Paris, France.
Jacques CallebertAssistance Publique Hôpitaux de Paris, Service de Biochimie and INSERM U942, Hôpital Lariboisière, Paris, France.
Alain TedguiUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.ORCID 0000-0002-7229-4875
Hafid Ait-OufellaUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France.ORCID 0000-0002-2955-0183
Harry SokolSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, CRSA, AP-HP, Saint Antoine Hospital, Gastroenterology Department, F-75012, Paris, France.ORCID 0000-0002-2914-1822
Benoit ChassaingMicrobiome-Host interactions, Institut Pasteur, Université Paris Cité, INSERM U1306, Paris, France.ORCID 0000-0002-4285-769X
Soraya TalebUniversité Paris Cité, Inserm, PARCC, F-75015, Paris, France. soraya.taleb@inserm.fr.ORCID 0000-0002-6650-619X

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-22CE14-0014-01
6 · The paper itself

Abstract

Tryptophan (Trp) is an essential amino acid, whose metabolism is a key gatekeeper of intestinal homeostasis. Yet, its systemic effects, particularly on atherosclerosis, remain unknown. Here we show that high-fat diet (HFD) increases the activity of intestinal indoleamine 2, 3-dioxygenase 1 (IDO), which shifts Trp metabolism from the production of microbiota-derived indole metabolites towards kynurenine production. Under HFD, the specific deletion of IDO in intestinal epithelial cells leads to intestinal inflammation, impaired intestinal barrier, augmented lesional T lymphocytes and atherosclerosis. This is associated with an increase in serotonin production and a decrease in indole metabolites, thus hijacking Trp for the serotonin pathway. Inhibition of intestinal serotonin production or supplementation with indole derivatives alleviates plaque inflammation and atherosclerosis. In summary, we uncover a pivotal role of intestinal IDO in the fine-tuning of Trp metabolism with systemic effects on atherosclerosis, paving the way for new therapeutic strategies to relieve gut-associated inflammatory diseases.

Indexed as

AtherosclerosisDiet, High-FatIndoleamine-Pyrrole 2,3,-DioxygenaseIntestinal MucosaMice, Inbred C57BLSerotoninTryptophanAnimalsDisease Models, AnimalGastrointestinal MicrobiomeIndolesInflammationIntestinesKynurenineMaleMiceIDO1 protein, mouseIndoleamine-Pyrrole 2,3,-DioxygenaseIndolesKynurenineSerotoninTryptophan

Identifiers

PMID39080345
PMCPMC11289133

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.