Evidence map›Paper›PMID 24875100›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2014

Increased acid responsiveness in vagal sensory neurons in a guinea pig model of eosinophilic esophagitis.

Youtian Hu, Zhenyu Liu, Xiaoyun Yu, Pankaj J Pasricha, Bradley J Undem, Shaoyong Yu

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.3field-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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Mouse models of eosinophilic esophagitis: molecular and translational insights.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Review
  2. Animal models of eosinophilic esophagitis.Journal of leukocyte biology · 2024
    Review
  3. Review
  4. Article
  5. Review
  6. Deoxycholic acid activates and sensitizes vagal nociceptive afferent C-fibers in guinea pig esophagus.American journal of physiology. Gastrointestinal and liver physiology · 2021
    Article
  7. Review
  8. Article
  9. Management of refractory eosinophilic oesophagitis.Nature reviews. Gastroenterology & hepatology · 2017
    Review
  10. TRP channel functions in the gastrointestinal tract.Seminars in immunopathology · 2016
    Review
  11. Mechanisms of the adenosine A2A receptor-induced sensitization of esophageal C fibers.American journal of physiology. Gastrointestinal and liver physiology · 2016
    Article
  12. Article
  13. Eosinophilic Esophagitis and Gastroenteritis.Current allergy and asthma reports · 2015
    Review
  14. Allergen challenge sensitizes TRPA1 in vagal sensory neurons and afferent C-fiber subtypes in guinea pig esophagus.American journal of physiology. Gastrointestinal and liver physiology · 2015
    Article
  15. TRPM8 function and expression in vagal sensory neurons and afferent nerves innervating guinea pig esophagus.American journal of physiology. Gastrointestinal and liver physiology · 2015
    Article
  16. Article
  17. Role of satellite glial cells in gastrointestinal pain.Frontiers in cellular neuroscience · 2015
    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

6 authors at 2 institutions in 1 country.

Youtian HuDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Zhenyu LiuDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Xiaoyun YuDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Pankaj J PasrichaDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Bradley J UndemDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Shaoyong YuDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland syyu@jhmi.edu.
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

Institute for Clinical and Translational ResearchUL1TR001079 · NCATS · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2013 to 2017
$60.1M
Translational Research Enhancement CoreP30DK089502 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI ZACHOS, NICHOLAS CONSTANTINE · 2011 to 2020
$12.0M
Esophageal Mast Cell Nerve InteractionsR01DK087991 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YU, SHAOYONG · 2010 to 2014
$1.3M
NCATS NIH HHS UL1 TR001079NIDDK NIH HHS DK-087991NIDDK NIH HHS P30 DK089502NIDDK NIH HHS R01 DK087991
6 · The paper itself

Abstract

Eosinophilic esophagitis (EoE) is characterized with eosinophils and mast cells predominated allergic inflammation in the esophagus and present with esophageal dysfunctions such as dysphagia, food impaction, and heartburn. However, the underlying mechanism of esophageal dysfunctions is unclear. This study aims to determine whether neurons in the vagal sensory ganglia are modulated in a guinea pig model of EoE. Animals were actively sensitized by ovalbumin (OVA) and then challenged with aerosol OVA inhalation for 2 wk. This results in a mild esophagitis with increases in mast cells and eosinophils in the esophageal wall. Vagal nodose and jugular neurons were disassociated, and their responses to acid, capsaicin, and transient receptor potential vanilloid type 1 (TRPV1) antagonist AMG-9810 were studied by calcium imaging and whole cell patch-clamp recording. Compared with naïve animals, antigen challenge significantly increased acid responsiveness in both nodose and jugular neurons. Their responses to capsaicin were also increased after antigen challenge. AMG-9810, at a concentration that blocked capsaicin-evoked calcium influx, abolished the increase in acid-induced activation in both nodose and jugular neurons. Vagotomy strongly attenuated those increased responses of nodose and jugular neurons to both acid and capsaicin induced by antigen challenge. These data for the first time demonstrated that prolonged antigen challenge significantly increases acid responsiveness in vagal nodose and jugular ganglia neurons. This sensitization effect is mediated largely through TRPV1 and initiated at sensory nerve endings in the peripheral tissues. Allergen-induced enhancement of responsiveness to noxious stimulation by acid in sensory nerve may contribute to the development of esophageal dysfunctions such as heartburn in EoE.

Indexed as

AcrylamidesAnimalsBridged Bicyclo Compounds, HeterocyclicCalcium SignalingCapsaicinDisease Models, AnimalDose-Response Relationship, DrugEosinophilic EsophagitisEsophagusGuinea PigsHeartburnHydrogen-Ion ConcentrationMaleMembrane PotentialsNodose GanglionOvalbumin3-(4-t-butylphenyl)-N-(2,3-dihydrobenzo(b)(1,4)dioxin-6-yl)acrylamideAcrylamidesBridged Bicyclo Compounds, HeterocyclicCapsaicinOvalbuminTRPV Cation Channelsantigentransient receptor potential vanilloid type 1

Identifiers

PMID24875100
PMCPMC4101676
OpenAlexW2051944884

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.