Evidence map›Paper›PMID 21474426›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2011

Ion transport mechanisms linked to bicarbonate secretion in the esophageal submucosal glands.

Solange Abdulnour-Nakhoul, Hani N Nakhoul, Medhat I Kalliny, Alex Gyftopoulos, Edd Rabon, Rienk Doetjes, Karen Brown, Nazih L Nakhoul

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Ussing Chamber Methods to Study the Esophageal Epithelial Barrier.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  3. Advances in CaExperimental and therapeutic medicine · 2020
    Review
  4. Lubiprostone protects esophageal mucosa from acid injury in porcine esophagus.American journal of physiology. Gastrointestinal and liver physiology · 2020
    Article
  5. Review
  6. Review
  7. Article
  8. CaOncotarget · 2017
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. 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

8 authors at 2 institutions in 1 country.

Solange Abdulnour-NakhoulSoutheast Louisiana Veterans Health Care Network, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA. solange@tulane.edu
Hani N Nakhoul
Medhat I Kalliny
Alex Gyftopoulos
Edd Rabon
Rienk Doetjes
Karen Brown
Nazih L Nakhoul
Southeast Louisiana Veterans Health Care System · USTulane University · US

Funding

Membrane Transport of NH3 and NH4+R01DK062295 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI NAKHOUL, NAZIH · 2003 to 2008
$1.5M
NIDDK NIH HHS DK-62295
6 · The paper itself

Abstract

The esophageal submucosal glands (SMG) secrete HCO(3)(-) and mucus into the esophageal lumen, where they contribute to acid clearance and epithelial protection. This study characterized the ion transport mechanisms linked to HCO(3)(-) secretion in SMG. We localized ion transporters using immunofluorescence, and we examined their expression by RT-PCR and in situ hybridization. We measured HCO(3)(-) secretion by using pH stat and the isolated perfused esophagus. Using double labeling with Na(+)-K(+)-ATPase as a marker, we localized Na(+)-coupled bicarbonate transporter (NBCe1) and Cl(-)-HCO(3)(-) exchanger (SLC4A2/AE2) to the basolateral membrane of duct cells. Expression of cystic fibrosis transmembrane regulator channel (CFTR) was confirmed by immunofluorescence, RT-PCR, and in situ hybridization. We identified anion exchanger SLC26A6 at the ducts' luminal membrane and Na(+)-K(+)-2Cl(-) (NKCC1) at the basolateral membrane of mucous and duct cells. pH stat experiments showed that elevations in cAMP induced by forskolin or IBMX increased HCO(3)(-) secretion. Genistein, an activator of CFTR, which does not increase intracellular cAMP, also stimulated HCO(3)(-) secretion, whereas glibenclamide, a Cl(-) channel blocker, and bumetanide, a Na(+)-K(+)-2Cl(-) blocker, decreased it. CFTR(inh)-172, a specific CFTR channel blocker, inhibited basal HCO(3)(-) secretion as well as stimulation of HCO(3)(-) secretion by IBMX. This is the first report on the presence of CFTR channels in the esophagus. The role of CFTR in manifestations of esophageal disease in cystic fibrosis patients remains to be determined.

Indexed as

AnimalsAntiportersBicarbonatesCystic Fibrosis Transmembrane Conductance RegulatorEsophagusHydrogen-Ion ConcentrationIon TransportModels, AnimalMucous MembraneSodium-Potassium-Chloride SymportersSodium-Potassium-Exchanging ATPaseSwineAntiportersBicarbonatesCystic Fibrosis Transmembrane Conductance RegulatorSodium-Potassium-Chloride SymportersSodium-Potassium-Exchanging ATPase

Identifiers

PMID21474426
PMCPMC3129871
OpenAlexW1997998072

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.