Evidence map›Paper›PMID 26263434›Full record

ArticleShock (Augusta, Ga.)2015

Plasma-Mediated Gut Protection After Hemorrhagic Shock is Lessened in Syndecan-1-/- Mice.

Kechen Ban, Zhanglong Peng, Shibani Pati, Richard B Witkov, Pyong Woo Park, Rosemary A Kozar

Open access · greenAbstract read
In one paragraph

Article in Shock (Augusta, Ga.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Trauma-induced coagulopathy.Nature reviews. Disease primers · 2021
    Review
  5. Review
  6. Review
  7. Traumatic brain injury is associated with increased syndecan-1 shedding in severely injured patients.Scandinavian journal of trauma, resuscitation and emergency medicine · 2018
    Observational
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
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

6 authors at 2 institutions in 2 countries.

Kechen Ban*Department of Pathology and Immunology, Baylor College of Medicine, Houston, Texas †Shock Trauma Center, University of Maryland, Baltimore, Maryland ‡Blood Systems Research Institute §Department of Surgery, University of California, San Francisco, California ||University of Texas Health Science Center at Houston, Houston, Texas ¶Division of Respiratory Diseases, Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Zhanglong Peng
Shibani Pati
Richard B Witkov
Pyong Woo Park
Rosemary A Kozar
Government of the United Kingdom · GBUniversity of Maryland, Baltimore · US

Funding

Syndecan shedding after trauma and hemorrhagic shockR01GM107482 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KOZAR, ROSEMARY A · 2013 to 2016
$1.2M
NIGMS NIH HHS R01 GM107482NIGMS NIH HHS R01GM107482
6 · The paper itself

Abstract

We have shown in a rodent model of hemorrhagic shock (HS) that fresh frozen plasma (FFP) reduces lung inflammation and injury that are correlated with restitution of syndecan-1. As the gut is believed to contribute to distant organ injury and inflammation after shock, the current study sought to determine if the protective effects of plasma would extend to the gut and to elucidate the contribution of syndecan-1 to this protective effect. We also examined the potential role of TNFα, and a disintegrin and metalloproteinase (ADAM)-17, both intestinal sheddases of syndecan-1. Wild-type (WT) and syndecan-1 (KO) mice were subjected to HS followed by resuscitation with lactated Ringer's (LR) or FFP and compared with shock alone and shams. Small bowel and blood were obtained after 3  h for analysis of mucosal injury and inflammation and TNFα and ADAM-17 protein expression and activity. After HS, gut injury and inflammation were significantly increased compared with shams. Resuscitation with LR decreased both injury and inflammation that were further lessened by FFP. KO mice displayed worsened gut injury and inflammation after HS compared with WT mice, and LR and FFP equivalently inhibited injury and inflammation. Both systemic and intestinal TNFα and ADAM-17 followed similar trends, with increases after HS, reduction by LR, and a further decrease by FFP in WT but not KO mice. In conclusion, FFP decreased gut injury and inflammation after hemorrhagic shock, an effect that was abrogated in syndecan-1 mice. Plasma also decreased TNFα and ADAM-17, representing a potential mechanistic link to its protection via syndecan-1.

Indexed as

PlasmaADAM17 ProteinADAM ProteinsAnimalsDisease Models, AnimalEnteritisIntestinal DiseasesIntestinal MucosaIntestine, SmallMaleMice, KnockoutShock, HemorrhagicSyndecan-1Tumor Necrosis Factor-alphaADAM17 ProteinAdam17 protein, mouseADAM ProteinsSdc1 protein, mouseSyndecan-1Tumor Necrosis Factor-alpha

Identifiers

PMID26263434
PMCPMC4816460
OpenAlexW2395794835

What OpenQuestion holds

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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.