Evidence map›Paper›PMID 22586225›Full record

ArticleThe Journal of physiology2012

The electroneutral Na⁺:HCO₃⁻ cotransporter NBCn1 is a major pHi regulator in murine duodenum.

Mingmin Chen, Jeppe Praetorius, Wen Zheng, Fang Xiao, Brigitte Riederer, Anurag Kumar Singh, Nicole Stieger, Jian Wang, Gary E Shull, Christian Aalkjaer and 1 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. The electroneutral NaAmerican journal of physiology. Cell physiology · 2024
    Article
  3. Bicarbonate secretion and acid/base sensing by the intestine.Pflugers Archiv : European journal of physiology · 2024
    Review
  4. Article
  5. Understanding the Physiological Role of Electroneutral NaPharmaceuticals (Basel, Switzerland) · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Advances in CaExperimental and therapeutic medicine · 2020
    Review
  10. Review
  11. Article
  12. Mouse models of SLC4-linked disorders of HCOAmerican journal of physiology. Cell physiology · 2018
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Cation-coupled bicarbonate transporters.Comprehensive Physiology · 2014
    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

11 authors at 3 institutions in 3 countries.

Mingmin ChenDepartment of Gastroenterology, Hannover Medical School, Carl-Neuberg-Straße 1, Hannover, D-30625, Germany.
Jeppe Praetorius
Wen Zheng
Fang Xiao
Brigitte Riederer
Anurag Kumar Singh
Nicole Stieger
Jian Wang
Gary E Shull
Christian Aalkjaer
Ursula Seidler
Medizinische Hochschule Hannover · DEAarhus University · DKUniversity of Cincinnati · US

Funding

MODELS FOR GENETIC DISORDERS OF ACID-BASE TRANSPORTR37DK050594 · NIDDK · UNIVERSITY OF CINCINNATI · PI SHULL, GARY EDWARD · 2000 to 2009
$6.0M
MODELS FOR GENETIC DISORDERS OF ACID BASE TRANSPORTR01DK050594 · NIDDK · UNIVERSITY OF CINCINNATI · PI SHULL, GARY EDWARD · 1996 to 2013
$1.9M
NIDDK NIH HHS DK050594NIDDK NIH HHS R01 DK050594NIDDK NIH HHS R37 DK050594
6 · The paper itself

Abstract

Duodenocyte pHi control and HCO3 − secretion protects the proximal duodenum against damage by gastric acid. The molecular details of duodenocyte pH control are not well understood. A selective duodenal expression (within the upper GI tract) has been reported for the electroneutral Na+:HCO3 − cotransporter NBCn1 (Slc4a7). We aimed to determine the role of NBCn1 and NBCe2 in duodenocyte intracellular pH regulation as well as basal and agonist-stimulated duodenal bicarbonate secretion (JHCO3 −), exploiting mouse models of genetic slc4a7 and slc4a5 disruption. Basal and forskolin (FSK)-stimulated JHCO3 − was measured by single-pass perfusion in the duodenum of slc4a7−/− and slc4a7+/+ as well as slc4a5−/− and slc4a5+/+ mice in vivo, and by pH-stat titration in isolated duodenal mucosa in vitro. Duodenocyte HCO3 − uptake rates were fluorometrically assessed after acidification of intact villi and of isolated duodenocytes. Slc4a7−/− mice displayed significantly lower basal and FSK-stimulated duodenal HCO3 − secretion than slc4a7+/+ littermates in vivo. FSK-stimulated HCO3 − secretion was significantly reduced in slc4a7−/− isolated duodenal mucosa. Na+- and HCO3 −-dependent base uptake rates were significantly decreased in slc4a7−/− compared with slc4a7+/+ villus duodenocytes when measured in intact villi. Carbonic anhydrase (CA)-mediated CO2 hydration played no apparent role as a HCO3 − supply mechanism for basal or FSK-stimulated secretion in the slc4a7+/+ duodenum, but was an important alternative HCO3 − supply mechanism in the slc4a7−/− duodenum. NBCe2 (Slc4a5) displayed markedly lower duodenal mRNA expression levels, and its disruption did not interfere with duodenal HCO3 − secretion. The electroneutral Na+:HCO3 − cotransporter NBCn1 (slc4a7) is a major duodenal HCO3 − importer that supplies HCO3 − during basal and FSK-stimulated HCO3 − secretion.

Indexed as

AnimalsBicarbonatesCarbon DioxideCarbonic AnhydrasesColforsinDuodenumHydrogen-Ion ConcentrationIntestinal MucosaMiceMice, Inbred C57BLMice, KnockoutRNA, MessengerSodiumSodium-Bicarbonate SymportersBicarbonatesCarbon DioxideCarbonic AnhydrasesColforsinRNA, MessengerSLC4A5 protein, mouseSlc4a7 protein, mouseSodiumSodium-Bicarbonate Symporters

Identifiers

PMID22586225
PMCPMC3459045
OpenAlexW2149915104

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.