Evidence map›Paper›PMID 18682519›Full record

ArticleGut2008

CO2 chemosensing in rat oesophagus.

Y Akiba, M Mizumori, M Kuo, M Ham, P H Guth, E Engel, J D Kaunitz

Open access · greenAbstract read
In one paragraph

Article in Gut, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 57 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Review
  7. Upregulation of acid sensing ion channels is associated with esophageal hypersensitivity in GERD.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  8. Review
  9. Article
  10. Review
  11. Short-chain fatty acid sensing in rat duodenum.The Journal of physiology · 2015
    Article
  12. Article
  13. ENaCs and ASICs as therapeutic targets.American journal of physiology. Cell physiology · 2012
    Review
  14. ATP: a mediator for HCl-induced TRPV1 activation in esophageal mucosa.American journal of physiology. Gastrointestinal and liver physiology · 2011
    Article
  15. Review
  16. ASIC3 channels in multimodal sensory perception.ACS chemical neuroscience · 2011
    Review
  17. Luminal chemosensing in the duodenal mucosa.Acta physiologica (Oxford, England) · 2011
    Review
  18. Article
  19. Review
  20. 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

7 authors at 2 institutions in 1 country.

Y AkibaDepartment of Medicine, School of Medicine, Los Angeles, California, USA.
M Mizumori
M Kuo
M Ham
P H Guth
E Engel
J D Kaunitz
University of California, Los Angeles · USVA Greater Los Angeles Healthcare System · US

Funding

Duodenal Muscosal Defense MechanismsR01DK054221 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KAUNITZ, JONATHAN D. · 1999 to 2016
$4.4M
BLRD VA I01 BX001245NIDDK NIH HHS R01 DK054221NIDDK NIH HHS R01 DK54221
6 · The paper itself

Abstract

backgroundAcid in the oesophageal lumen is often sensed as heartburn. It was hypothesised that luminal CO(2), a permeant gas, rather than H(+), permeates through the epithelium, and is converted to H(+), producing an afferent neural signal by activating chemosensors.

methodsThe rat lower oesophageal mucosa was superfused with pH 7.0 buffer, and pH 1.0 or pH 6.4 high CO(2) (P(CO2) = 260 Torr) solutions with or without the cell-permeant carbonic anhydrase (CA) inhibitor methazolamide (MTZ, 1 mM), the cell-impermeant CA inhibitor benzolamide (BNZ, 0.1 mM), the transient receptor potential vanilloid 1 (TRPV1) antagonist capsazepine (CPZ, 0.5 mM) or the acid-sensing ion channel (ASIC) inhibitor amiloride (0.1 mM). Interstitial pH (pH(int)) was measured with 5',6'-carboxyfluorescein (5 mg/kg intravenously) loaded into the interstitial space, and blood flow was measured with laser-Doppler.

resultsPerfusion of a high CO(2) solution induced hyperaemia without changing pH(int), mimicking the effect of pH 1.0 perfusion. Perfused MTZ, BNZ, CPZ and amiloride all inhibited CO(2)-induced hyperaemia. CA XIV was expressed in the prickle cells, with CA XII in the basal cells. TRPV1 was expressed in the stratum granulosum and in the muscularis mucosa, whereas all ASICs were expressed in the prickle cells, with ASIC3 additionally in the muscularis mucosa.

conclusionsThe response to CO(2) perfusion suggests that CO(2) diffuses through the stratum epithelium, interacting with TRPV1 and ASICs in the epithelium or in the submucosa. Inhibition of the hyperaemic response to luminal CO(2) by CA, TRPV1 and ASIC inhibitors implicates CA and these chemosensors in transduction of the luminal acid signal. Transepithelial CO(2) permeation may explain how luminal H(+) equivalents can rapidly be transduced into hyperaemia, and the sensation of heartburn.

Indexed as

Acid Sensing Ion ChannelsAmilorideAnimalsBenzolamideCapsaicinCarbon DioxideCarbonic Anhydrase InhibitorsEpithelial CellsEsophageal pH MonitoringEsophagusGastroesophageal RefluxHyperemiaMaleMethazolamideMucous MembraneNerve Tissue ProteinsAcid Sensing Ion ChannelsAmilorideASIC3 protein, ratBenzolamideCapsaicincapsazepineCarbon DioxideCarbonic Anhydrase InhibitorsMethazolamideNerve Tissue ProteinsSodium ChannelsTrpv1 protein, ratTRPV Cation Channels

Identifiers

PMID18682519
PMCPMC4861555
OpenAlexW2120973569

What OpenQuestion holds

Textmetadata
LicenceTDM
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.