Evidence map›Paper›PMID 9410903›Full record

ArticleThe Journal of clinical investigation1997

Pretreatment with antibody to eosinophil major basic protein prevents hyperresponsiveness by protecting neuronal M2 muscarinic receptors in antigen-challenged guinea pigs.

C M Evans, A D Fryer, D B Jacoby, G J Gleich, R W Costello

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
5.1field-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

68 citing papers in PubMed, 184 citations in OpenAlex.

  1. Optogenetic vagotomy inhibits reflex bronchoconstriction and cardiac chronotropy.American journal of respiratory cell and molecular biology · 2026
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  2. Review
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  6. Review
  7. Eosinophils prevent diet-induced airway hyperresponsiveness in mice on a high-fat diet.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  8. Review
  9. Unique Allergic Asthma Phenotypes in Offspring of House Dust Mite-exposed Mice.American journal of respiratory cell and molecular biology · 2022
    Article
  10. Review
  11. Article
  12. Review
  13. Optogenetic Control of Airway Cholinergic NeuronsAmerican journal of respiratory cell and molecular biology · 2020
    Article
  14. IL-5 ExposureAmerican journal of respiratory cell and molecular biology · 2020
    Article
  15. Lung eosinophils increase vagus nerve-mediated airway reflex bronchoconstriction in mice.American journal of physiology. Lung cellular and molecular physiology · 2020
    Article
  16. Airway Innervation and Plasticity in Asthma.Physiology (Bethesda, Md.) · 2019
    Review
  17. Mechanisms of organophosphorus pesticide toxicity in the context of airway hyperreactivity and asthma.American journal of physiology. Lung cellular and molecular physiology · 2018
    Review
  18. Eosinophil and airway nerve interactions in asthma.Journal of leukocyte biology · 2018
    Review
  19. Article
  20. Protective Role of Eosinophils and TNFa after Ozone Inhalation.Research report (Health Effects Institute) · 2017
    Article

8 more citing papers are in PubMed but not listed here.

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

5 authors at 4 institutions in 2 countries.

C M EvansDepartment of Environmental Health Sciences, School of Hygiene and Public Health, Johns Hopkins University, Baltimore, Maryland 21205, USA.
A D Fryer
D B Jacoby
G J Gleich
R W Costello
Johns Hopkins University · USJohns Hopkins Medicine · USMayo Clinic · USMinistère de la Santé et de l'Hygiène Publique · ML

Funding

PILOT STUDY--ACID FOG, AN EXPERIMENTAL MODELP30ES003819 · NIEHS · JOHNS HOPKINS UNIVERSITY · PI GROOPMAN, JOHN D · 1985 to 2012
$22.6M
VIRAL ENZYMES &NEURONAL MUSCARINIC RECEPTORS IN LUNGR29HL044727 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI FRYER, ALLISON DEBORAH · 1991 to 1995
–
NHLBI NIH HHS HL-44727NHLBI NIH HHS HL-53543NIEHS NIH HHS ES-03819
6 · The paper itself

Abstract

In antigen-challenged guinea pigs there is recruitment of eosinophils into the lungs and to airway nerves, decreased function of inhibitory M2 muscarinic autoreceptors on parasympathetic nerves in the lungs, and airway hyperresponsiveness. A rabbit antibody to guinea pig eosinophil major basic protein was used to determine whether M2 muscarinic receptor dysfunction, and the subsequent hyperresponsiveness, are due to antagonism of the M2 receptor by eosinophil major basic protein. Guinea pigs were sensitized, challenged with ovalbumin and hyperresponsiveness, and M2 receptor function tested 24 h later with the muscarinic agonist pilocarpine. Antigen-challenged guinea pigs were hyperresponsive to electrical stimulation of the vagus nerves compared with controls. Likewise, loss of M2 receptor function was demonstrated since the agonist pilocarpine inhibited vagally-induced bronchoconstriction in control but not challenged animals. Pretreatment with rabbit antibody to guinea pig eosinophil major basic protein prevented hyperresponsiveness, and protected M2 receptor function in the antigen-challenged animals without inhibiting eosinophil accumulation in the lungs or around the nerves. Thus, hyperresponsiveness is a result of inhibition of neuronal M2 muscarinic receptor function by eosinophil major basic protein in antigen-challenged guinea pigs.

Indexed as

RibonucleasesAcetylcholineAnimalsAntigensAsthmaBlood ProteinsElectric StimulationEosinophil Granule ProteinsEosinophilsFemaleGuinea PigsImmunologic TechniquesOvalbuminRabbitsReceptor, Muscarinic M2Receptors, MuscarinicAcetylcholineAntigensBlood ProteinsEosinophil Granule ProteinsOvalbuminReceptor, Muscarinic M2Receptors, MuscarinicRibonucleases

Identifiers

PMID9410903
PMCPMC508421
OpenAlexW1999800943

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.