Evidence map›Paper›PMID 19703164›Full record

ReviewBritish journal of pharmacology2009

Arginase: a key enzyme in the pathophysiology of allergic asthma opening novel therapeutic perspectives.

Harm Maarsingh, Johan Zaagsma, Herman Meurs

Open access · bronzeAbstract readCommentReview
In one paragraph

Review in British journal of pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

59 citing papers in PubMed, 147 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Targeting alarmins in asthma: From bench to clinic.The Journal of allergy and clinical immunology · 2025
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Update on the Role of FeNO in Asthma Management.Diagnostics (Basel, Switzerland) · 2023
    Review
  14. Article
  15. Review
  16. Review
  17. Arginine Therapy for Lung Diseases.Frontiers in pharmacology · 2021
    Review
  18. Article
  19. Class C GPCRs in the airway.Current opinion in pharmacology · 2020
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Harm MaarsinghDepartment of Molecular Pharmacology, University of Groningen, Groningen, The Netherlands. h.maarsingh@rug.nl
Johan Zaagsma
Herman Meurs
University of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allergic asthma is a chronic inflammatory airways' disease, characterized by allergen-induced early and late bronchial obstructive reactions, airway hyperresponsiveness (AHR), airway inflammation and airway remodelling. Recent ex vivo and in vivo studies in animal models and asthmatic patients have indicated that arginase may play a central role in all these features. Thus, increased arginase activity in the airways induces reduced bioavailability of L-arginine to constitutive (cNOS) and inducible (iNOS) nitric oxide synthases, causing a deficiency of bronchodilating and anti-inflammatory NO, as well as increased formation of peroxynitrite, which may be involved in allergen-induced airways obstruction, AHR and inflammation. In addition, both via reduced NO production and enhanced synthesis of L-ornithine, increased arginase activity may be involved in airway remodelling by promoting cell proliferation and collagen deposition in the airway wall. Therefore, arginase inhibitors may have therapeutic potential in the treatment of acute and chronic asthma. This review focuses on the pathophysiological role of arginase in allergic asthma and the emerging effectiveness of arginase inhibitors in the treatment of this disease.

Indexed as

Airway RemodelingAnimalsAnti-Allergic AgentsAnti-Inflammatory AgentsArginaseAsthmaBronchial HyperreactivityHumansInflammationNitric OxideNitric Oxide SynthaseRespiratory Physiological PhenomenaAnti-Allergic AgentsAnti-Inflammatory AgentsArginaseNitric OxideNitric Oxide Synthase

Identifiers

PMID19703164
PMCPMC2765587
OpenAlexW2162852294

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.