Evidence map›Paper›PMID 9199469›Full record

ArticleInfection and immunity1997

Induction of nitric oxide synthesis and xanthine oxidase and their roles in the antimicrobial mechanism against Salmonella typhimurium infection in mice.

K Umezawa, T Akaike, S Fujii, M Suga, K Setoguchi, A Ozawa, H Maeda

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In one paragraph

Article in Infection and immunity, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

55 citing papers in PubMed, 152 citations in OpenAlex.

  1. Article
  2. Article
  3. Mechanisms of TLR4-Mediated Autophagy and Nitroxidative Stress.Frontiers in cellular and infection microbiology · 2021
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  4. Interplay between enterohaemorrhagicEmerging microbes & infections · 2020
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  6. Humoral Immunity vs.Frontiers in immunology · 2019
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  11. Article
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  13. Article
  14. Review
  15. Redox proteomics of protein-bound methionine oxidation.Molecular & cellular proteomics : MCP · 2011
    Article
  16. Nitric oxide and salmonella pathogenesis.Frontiers in microbiology · 2011
    Article
  17. Article
  18. Article
  19. Article
  20. Resistance to peroxynitrite in Neisseria gonorrhoeae.Microbiology (Reading, England) · 2009
    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

7 authors at 1 institution in 1 country.

K UmezawaDepartment of Microbiology, Kumamoto University School of Medicine, Honjo, Japan.
T Akaike
S Fujii
M Suga
K Setoguchi
A Ozawa
H Maeda
Sojo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of superoxide anion (O2-) and nitric oxide (NO) in the host defense mechanism against Salmonella typhimurium (LT-2) was examined by focusing on xanthine oxidase (XO) as an O2(-)-generating system and on inducible NO synthase (iNOS). When ICR mice were infected with a 0.1 50% lethal dose (2 x 10(5) CFU) of S. typhimurium, bacterial growth in the liver reached a peak value 3 days after infection (10(4.32) CFU/g of liver) and decreased thereafter. XO activity in the liver became maximum at 7 days after infection; the value was 34.6 +/- 1.4 mU/g of liver at 7 days (compared with 11.0 +/- 1.3 mU/g of liver before infection). The time profile of NO production in the liver as determined by electron spin resonance spectroscopy was consistent with that of XO activity. Histological examination of infected liver showed the formation of multiple microabscesses with granulomatous lesions consisting of polymorphonuclear cells and mononuclear cells, and iNOS-expressing cells were localized in the confined areas of the microabscesses. When XO inhibitors such as allopurinol and 4-amino-6-hydroxypyrazolo[3,4-d]pyrimidine (AHPP) were administered to the infected mice, the mortality of the mice was significantly increased (10 of 21 and 11 of 20 for the allopurinol- and AHPP-treated groups, respectively, versus 2 of 20 for control mice), and bacterial growth was significantly enhanced. A similar exacerbation of the infection was obtained with N(omega)-monomethyl-L-arginine (L-NMMA) treatment of the mice. Of considerable importance is that granuloma formation in the liver was poorly developed by treatment with either XO inhibitors or L-NMMA. These results suggest that XO and NO play an important role in the antimicrobial mechanism against S. typhimurium in mice.

Indexed as

Salmonella typhimuriumAllopurinolAnimalsAntimetabolitesEnzyme InhibitorsLiverMaleMiceMice, Inbred ICRNitric Oxideomega-N-MethylarginineSalmonella Infections, AnimalXanthine OxidaseAllopurinolAntimetabolitesEnzyme InhibitorsNitric Oxideomega-N-MethylarginineXanthine Oxidase

Identifiers

PMID9199469
PMCPMC175411
OpenAlexW2156041007

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.