Evidence map›Paper›PMID 31547920›Full record

ArticleThe American journal of pathology2019

Endogenous Specialized Proresolving Mediator Profiles in a Novel Experimental Model of Lymphatic Obstruction and Intestinal Inflammation in African Green Monkeys.

Felix Becker, Emily Romero, Jason Goetzmann, Dana L Hasselschwert, Beth Dray, John Vanchiere, Jane Fontenot, J Winny Yun, Paul C Norris, Luke White and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 23% of its field
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Are EPA and DHA Derivatives Involved in IBD Remission?Journal of clinical medicine · 2022
    Article
  4. Article
  5. Article
  6. Specialized Pro-Resolving Mediators and the Lymphatic System.International journal of molecular sciences · 2021
    Review
  7. Article
  8. 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

14 authors at 7 institutions in 3 countries.

Felix BeckerDepartment of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center-Shreveport, Shreveport, Louisiana; Department of General, Visceral and Transplant Surgery, University of Münster, Münster, Germany.
Emily RomeroNew Iberia Research Center, University of Louisiana at Lafayette, New Iberia, Louisiana.
Jason GoetzmannNew Iberia Research Center, University of Louisiana at Lafayette, New Iberia, Louisiana.
Dana L HasselschwertNew Iberia Research Center, University of Louisiana at Lafayette, New Iberia, Louisiana.
Beth DrayDepartment of Veterinary Science and Keeling Center for Comparative Medicine and Research, The University of Texas MD Anderson Cancer Center, Bastrop, Texas.
John VanchiereSection of Pediatric Infectious Diseases, Department of Pediatrics, Louisiana State University Health Sciences Center-Shreveport, Shreveport, Louisiana.
Jane FontenotNew Iberia Research Center, University of Louisiana at Lafayette, New Iberia, Louisiana.
J Winny YunDepartment of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center-Shreveport, Shreveport, Louisiana.
Paul C NorrisCenter for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative, and Pain Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Luke WhiteDepartment of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center-Shreveport, Shreveport, Louisiana.
Melany MussoNew Iberia Research Center, University of Louisiana at Lafayette, New Iberia, Louisiana.
Charles N SerhanCenter for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative, and Pain Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
J Steven AlexanderDepartment of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center-Shreveport, Shreveport, Louisiana; Department of Neurology, Louisiana State University Health Sciences Center-Shreveport, Shreveport, Louisiana.
Felicity N E GavinsDepartment of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center-Shreveport, Shreveport, Louisiana; Department of Life Sciences, Brunel University London, London, United Kingdom. Electronic address: fgavin@lsuhsc.edu.
University of Louisiana at Lafayette · USBrigham and Women's Hospital · USLouisiana State University Health Sciences Center Shreveport · USLouisiana State University in Shreveport · USBrunel University of London · GBThe University of Texas MD Anderson Cancer Center · USUniversity of Münster · DE

Funding

Resolution Mechanisms in Acute Inflammation: Resolution PharmacologyP01GM095467 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI PETASIS, NICOS A · 2011 to 2020
$14.8M
Investigating the dysfunction of the cerebral microvasculature in sickle cell diseaseR01HL134959 · NHLBI · LOUISIANA STATE UNIV HSC SHREVEPORT · PI STOKES, KAREN Y · 2017 to 2020
$1.4M
NHLBI NIH HHS R01 HL134959NIGMS NIH HHS P01 GM095467
6 · The paper itself

Abstract

Changes in the intestinal lymphatic vascular system, such as lymphatic obstruction, are characteristic features of inflammatory bowel diseases. The lymphatic vasculature forms a conduit to enable resolution of inflammation; this process is driven by specialized endogenous proresolving mediators (SPMs). To evaluate contributions of lymphatic obstruction to intestinal inflammation and to study profiles of SPMs, we generated a novel animal model of lymphatic obstruction using African green monkeys. Follow-up studies were performed at 7, 21, and 61 days. Inflammation was determined by histology. Luminex assays were performed to evaluate chemokine and cytokine levels. In addition, lipid mediator metabololipidomic profiling was performed to identify SPMs. After 7 days, lymphatic obstruction resulted in a localized inflammatory state, paralleled by an increase in inflammatory chemokines and cytokines, which were found to be up-regulated after 7 days but returned to baseline after 21 and 61 days. At the same time, a distinct pattern of SPMs was profiled, with an increase for D-series resolvins, protectins, maresins, and lipoxins at 61 days. These results indicate that intestinal lymphatic obstruction can lead to an acute inflammatory state, accompanied by an increase in proinflammatory mediators, followed by a phase of resolution, paralleled by an increase and decrease of respective SPMs.

Indexed as

Disease Models, AnimalAnimalsChlorocebus aethiopsInflammationInflammation MediatorsIntestinal DiseasesLipid MetabolismLipidsLymphatic DiseasesMaleInflammation MediatorsLipids

Identifiers

PMID31547920
PMCPMC6880773
OpenAlexW2974351289

What OpenQuestion holds

Textmetadata
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.