Evidence map›Paper›PMID 19136577›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2009

Mechanisms of eosinophil major basic protein-induced hyperexcitability of vagal pulmonary chemosensitive neurons.

Qihai Gu, Michelle E Lim, Gerald J Gleich, Lu-Yuan Lee

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

30 citing papers in PubMed, 40 citations in OpenAlex.

  1. Neuroplasticity and neuroimmune interactions with type 2 inflammation in asthma.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  2. Article
  3. Review
  4. The diversity of neuroimmune circuits controlling lung inflammation.American journal of physiology. Lung cellular and molecular physiology · 2023
    Review
  5. Review
  6. KThe Journal of physiology · 2022
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Cough responses to inhaled irritants are enhanced by eosinophil major basic protein in awake mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2019
    Article
  14. Article
  15. Eosinophil and airway nerve interactions in asthma.Journal of leukocyte biology · 2018
    Review
  16. Review
  17. Article
  18. Article
  19. Review
  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

4 authors at 1 institution in 1 country.

Qihai GuDepartment of Physiology, University of Kentucky Medical Center, Lexington, Kentucky 40536-0298, USA.
Michelle E Lim
Gerald J Gleich
Lu-Yuan Lee
University of Kentucky · US

Funding

THE FUNCTIONS OF EOSINOPHILSR01AI009728 · NIAID · UNIVERSITY OF UTAH · PI GLEICH, GERALD J · 1985 to 2006
$2.4M
CHEMOSENSITIVITY OF TACHYKININ CONTAINING LUNG AFFERENTSR01HL058686 · NHLBI · UNIVERSITY OF KENTUCKY · PI LEE, LU-YUAN · 1998 to 2008
$1.3M
PULMONARY C-NEURON HYPERSENSITIVITY:CELLULAR MECHANISMSR01HL067379 · NHLBI · UNIVERSITY OF KENTUCKY · PI LEE, LU-YUAN · 2002 to 2005
$1.1M
Pulmonary C-Neuron Hypersensitivity: Cellular MechanismsR56HL067379 · NHLBI · UNIVERSITY OF KENTUCKY · PI LEE, LU-YUAN · 2007 to 2007
$293k
THE FUNCTIONS OF EOSINOPHILSR37AI009728 · NIAID · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI GLEICH, GERALD J · 1987 to 1996
–
NHLBI NIH HHS HL58686NHLBI NIH HHS HL67379NIAID NIH HHS AI09728
6 · The paper itself

Abstract

We have reported recently that eosinophil-derived basic proteins directly enhance the capsaicin- and electrical stimulation-evoked whole cell responses in rat pulmonary sensory neurons (19). Our present study further elucidates the mechanisms underlying the sensitization of pulmonary afferent nerves induced by these cationic proteins. Our results show that pretreatment with eosinophil major basic protein (MBP; 2 microM, 60 s) significantly enhanced the excitability of isolated rat vagal pulmonary chemosensitive neurons to acid and ATP in the current-clamp mode, but this potentiating effect was absent in the voltage-clamp recordings. The hyperexcitability induced by MBP was not prevented by the blockade of either transient receptor potential vanilloid type-1 receptor (TRPV1) selectively (inhibitor: AMG 9810; 1 microM, 2 min) or all TRPV1-4 channels (inhibitor: ruthenium red; 5 microM, 2 min). In addition, MBP also markedly potentiated the excitability of mouse pulmonary chemosensitive neurons, and no detectable difference was found between those isolated from wild-type and TRPV1 knockout mice. Furthermore, MBP pretreatment affected the decay time and recovery phase of the action potentials evoked by current injections and significantly inhibited both the sustained delayed-rectifier voltage-gated K(+) current (IK(dr)) and the A-type, fast-inactivating K(+) current (IK(a)) in these sensory neurons. In conclusion, our results indicate that the inhibition of IK(dr) and IK(a) should, at least in part, account for the hyperexcitability of pulmonary chemosensitive neurons induced by eosinophil-derived cationic proteins, whereas an interaction with TRPV1 channels does not seem to be required for the sensitizing effect of these proteins.

Indexed as

Action PotentialsAnimalsEosinophil Major Basic ProteinHumansIn Vitro TechniquesLungMiceMice, Inbred C57BLMice, KnockoutPatch-Clamp TechniquesPotassium Channels, Voltage-GatedRatsRats, Sprague-DawleySensory Receptor CellsTRPV Cation ChannelsVagus NerveEosinophil Major Basic ProteinPotassium Channels, Voltage-GatedTRPV1 protein, mouseTrpv1 protein, ratTRPV Cation Channels

Identifiers

PMID19136577
PMCPMC2660213
OpenAlexW1984210151

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.