Evidence map›Paper›PMID 25591867›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2015

Allergen challenge sensitizes TRPA1 in vagal sensory neurons and afferent C-fiber subtypes in guinea pig esophagus.

Zhenyu Liu, Youtian Hu, Xiaoyun Yu, Jiefeng Xi, Xiaoming Fan, Chung-Ming Tse, Allen C Myers, Pankaj J Pasricha, Xingde Li, Shaoyong Yu

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Heartburn and dyspepsia symptom severity improves after treatment and correlates with histology in adults with eosinophilic esophagitis.Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus · 2019
    Trial
  2. Article
  3. Mouse models of eosinophilic esophagitis: molecular and translational insights.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Review
  4. Article
  5. Animal models of eosinophilic esophagitis.Journal of leukocyte biology · 2024
    Review
  6. Animal models of eosinophilic esophagitis, review and perspectives.Animal models and experimental medicine · 2024
    Review
  7. Eosinophilic Esophagitis: What's in a Name?Digestive diseases and sciences · 2024
    Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Mechanisms of organophosphorus pesticide toxicity in the context of airway hyperreactivity and asthma.American journal of physiology. Lung cellular and molecular physiology · 2018
    Review
  16. Article
  17. Review
  18. Ethyl Vanillin Activates TRPA1.The Journal of pharmacology and experimental therapeutics · 2017
    Article
  19. Article
  20. Biomedical physics & engineering express · 2017
    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

10 authors at 3 institutions in 2 countries.

Zhenyu LiuDivision of Gastroenterology, Peking University Shenzhen Hospital, Shenzhen, China; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland;
Youtian HuDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland;
Xiaoyun YuDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland;
Jiefeng XiDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland; and.
Xiaoming FanDivision of Gastroenterology and Hepatology, Jinshan Hospital of Fudan University, Shanghai, China.
Chung-Ming TseDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland;
Allen C MyersDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland;
Pankaj J PasrichaDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland;
Xingde LiDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland; and.
Shaoyong YuDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland; syyu@jhmi.edu.
Johns Hopkins University · USJohns Hopkins Medicine · USJinshan Hospital of Fudan University · CN

Funding

Esophageal Mast Cell Nerve InteractionsR01DK087991 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YU, SHAOYONG · 2010 to 2014
$1.3M
NIDDK NIH HHS DK087991NIDDK NIH HHS R01 DK087991
6 · The paper itself

Abstract

Transient receptor potential A1 (TRPA1) is a newly defined cationic ion channel, which selectively expresses in primary sensory afferent nerve, and is essential in mediating inflammatory nociception. Our previous study demonstrated that TRPA1 plays an important role in tissue mast cell activation-induced increase in the excitability of esophageal vagal nodose C fibers. The present study aims to determine whether prolonged antigen exposure in vivo sensitizes TRPA1 in a guinea pig model of eosinophilic esophagitis (EoE). Antigen challenge-induced responses in esophageal mucosa were first assessed by histological stains and Ussing chamber studies. TRPA1 function in vagal sensory neurons was then studied by calcium imaging and by whole cell patch-clamp recordings in 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI)-labeled esophageal vagal nodose and jugular neurons. Extracellular single-unit recordings were performed in vagal nodose and jugular C-fiber neuron subtypes using ex vivo esophageal-vagal preparations with intact nerve endings in the esophagus. Antigen challenge significantly increased infiltrations of eosinophils and mast cells in the esophagus. TRPA1 agonist allyl isothiocyanate (AITC)-induced calcium influx in nodose and jugular neurons was significantly increased, and current densities in esophageal DiI-labeled nodose and jugular neurons were also significantly increased in antigen-challenged animals. Prolonged antigen challenge decreased esophageal epithelial barrier resistance, which allowed intraesophageal-infused AITC-activating nodose and jugular C fibers at their nerve endings. Collectively, these results demonstrated that prolonged antigen challenge sensitized TRPA1 in esophageal sensory neurons and afferent C fibers. This novel finding will help us to better understand the molecular mechanism underlying esophageal sensory and motor dysfunctions in EoE.

Indexed as

AllergensOvalbuminAction PotentialsAnimalsCalcium SignalingDisease Models, AnimalEosinophilic EsophagitisEosinophilsEsophagusGuinea PigsIsothiocyanatesMaleMast CellsNerve Fibers, UnmyelinatedNodose GanglionSensationAllergensallyl isothiocyanateIsothiocyanatesOvalbuminTransient Receptor Potential Channelsdysphagiaeosinophilic esophagitisheartburnjugularnodose

Identifiers

PMID25591867
PMCPMC4360047
OpenAlexW2096063647

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.