Evidence map›Paper›PMID 19842024›Full record

ArticleInflammation2010

Carbon monoxide liberated from CO-releasing molecule (CORM-2) attenuates ischemia/reperfusion (I/R)-induced inflammation in the small intestine.

Kazuhiro Katada, Aurelia Bihari, Shinjiro Mizuguchi, Norimasa Yoshida, Toshikazu Yoshikawa, Douglas D Fraser, Richard F Potter, Gediminas Cepinskas

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
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  11. Microbiome and intestinal ischemia/reperfusion injury.Journal of clinical biochemistry and nutrition · 2018
    Review
  12. Article
  13. Article
  14. Article
  15. Carbon monoxide inhibits the nuclear-cytoplasmic translocation of HMGB1 in an in vitro oxidative stress injury model of mouse renal tubular epithelial cells.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2016
    Article
  16. Cytoprotective role of heme oxygenase-1 in liver ischemia reperfusion injury.International journal of clinical and experimental medicine · 2015
    Review
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 3 institutions in 2 countries.

Kazuhiro KatadaCentre for Critical Illness Research, Lawson Health Research Institute, 800 Commissioners Rd., London, ON, N6A4G5, Canada.
Aurelia Bihari
Shinjiro Mizuguchi
Norimasa Yoshida
Toshikazu Yoshikawa
Douglas D Fraser
Richard F Potter
Gediminas Cepinskas
Lawson Health Research Institute · CAKyoto Prefectural University of Medicine · JPWestern University · CA

Funding

Canadian Institutes of Health Research MOP-68848
6 · The paper itself

Abstract

CORM-released CO has been shown to be beneficial in resolution of acute inflammation. The acute phase of intestinal ischemia-reperfusion (I/R) injury is characterized by oxidative stress-related inflammation and leukocyte recruitment. In this study, we assessed the effects and potential mechanisms of CORM-2-released CO in modulation of inflammatory response in the small intestine following I/R-challenge. To this end mice (C57Bl/6) small intestine were challenged with ischemia by occluding superior mesenteric artery (SMA) for 45 min. CORM-2 (8 mg/kg; i.v.) was administered immediately before SMA occlusion. Sham operated mice were injected with vehicle (0.25% DMSO). Inflammatory response in the small intestine (jejunum) was assessed 4 h following reperfusion by measuring tissue levels of TNF-alpha protein (ELISA), adhesion molecules E-selectin and ICAM-1 (Western blot), NF-kappaB activation (EMSA), along with PMN tissue accumulation (MPO assay) and leukocyte rolling/adhesion in the microcirculation of jejunum (intravital microscopy). The obtained results indicate that tissue levels of TNF-alpha, E-selectin and ICAM-1 protein expression, activation of NF-kappaB, and subsequent accumulation of PMN were elevated in I/R-challenged jejunum. The above changes were significantly attenuated in CORM-2-treated mice. Taken together these findings indicate that CORM-2-released CO confers anti-inflammatory effects by interfering with NF-kappaB activation and subsequent up-regulation of vascular pro-adhesive phenotype in I/R-challenged small intestine.

Indexed as

AnimalsAnti-Inflammatory AgentsBlotting, WesternCarbon DioxideElectrophoretic Mobility Shift AssayEnzyme-Linked Immunosorbent AssayE-SelectinGastrointestinal AgentsInflammation MediatorsInflammatory Bowel DiseasesIntercellular Adhesion Molecule-1JejunumLeukocyte RollingMaleMesenteric Vascular OcclusionMiceAnti-Inflammatory AgentsCarbon DioxideE-SelectinGastrointestinal AgentsInflammation MediatorsIntercellular Adhesion Molecule-1NF-kappa BOrganometallic Compoundstricarbonyldichlororuthenium (II) dimerTumor Necrosis Factor-alpha

Identifiers

PMID19842024
OpenAlexW2037280078

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.