Evidence map›Paper›PMID 21148403›Full record

ArticleAmerican journal of physiology. Cell physiology2011

Reciprocal regulation of the primary sodium absorptive pathways in rat intestinal epithelial cells.

Steven Coon, Ramesh Kekuda, Prosenjit Saha, Uma Sundaram

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2011. 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
0.4field-weighted citation impact, top 36% 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, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Inhibition of intestinal villus cell Na/K-ATPase mediates altered glucose and NaCl absorption in obesity-associated diabetes and hypertension.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Small intestinal ion transport.Current opinion in gastroenterology · 2012
    Review
  17. 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

4 authors at 1 institution in 1 country.

Steven CoonWest Virginia Univ. School of Medicine, Morgantown, WV 26506, USA.
Ramesh Kekuda
Prosenjit Saha
Uma Sundaram
West Virginia University · US

Funding

REGULATION OF NA-NUTRIENT CO-TRANSPORTR01DK058034 · NIDDK · WEST VIRGINIA UNIVERSITY · PI SUNDARAM, UMA · 2000 to 2010
$3.0M
PATHOPHYSIOLOGY OF INTESTINAL SECRETION IN DIARRHEAR29DK045062 · NIDDK · YALE UNIVERSITY · PI SUNDARAM, UMA · 1993 to 2000
$95k
NIDDK NIH HHS DK45062NIDDK NIH HHS DK58034
6 · The paper itself

Abstract

Sodium absorption in the mammalian small intestine occurs predominantly by two primary pathways that include Na/H exchange (NHE3) and Na-glucose cotransport (SGLT1) on the brush border membrane (BBM) of villus cells. However, whether NHE3 and SGLT1 function together to regulate intestinal sodium absorption is unknown. Nontransformed small intestinal epithelial cells (IEC-18) were transfected with either NHE3 or SGLT1 small interfering RNAs (siRNAs) and were grown in confluent monolayers on transwell plates to measure the effects on Na absorption. Uptake studies were performed as well as molecular studies to determine the effects on NHE3 and SGLT1 activity. When IEC-18 monolayers were transfected with silencing NHE3 RNA, the cells demonstrated decreased NHE3 activity as well as decreased NHE3 mRNA and protein. However, in NHE3 siRNA-transected cells, SGLT1 activity, mRNA, and protein in the BBM were significantly increased. Thus, inhibition of NHE3 expression regulates the expression and function of SGLT1 in the BBM of intestinal epithelial cells. In addition, IEC-18 cells transected with silencing SGLT1 RNA demonstrated an inhibition of Na-dependent glucose uptake and a decrease in SGLT1 activity, mRNA, and protein levels. However, in these cells, Na/H exchange activity was significantly increased. Furthermore, NHE3 mRNA and protein levels were also increased. Therefore, the inhibition of SGLT1 expression stimulates the transcription and function of NHE3 and vice versa in the BBM of intestinal epithelial cells. Thus this study demonstrates that the major sodium absorptive pathways together function to regulate sodium absorption in epithelial cells.

Indexed as

AnimalsCell LineDown-RegulationFeedback, PhysiologicalGene Knockdown TechniquesIntestinal AbsorptionIntestinal MucosaMicrovilliRatsRNA, MessengerRNA, Small InterferingSignal TransductionSodiumSodium-Glucose Transporter 1Sodium-Hydrogen Exchanger 3Sodium-Hydrogen ExchangersRNA, MessengerRNA, Small InterferingSlc5a1 protein, ratSlc9a3 protein, ratSodiumSodium-Glucose Transporter 1Sodium-Hydrogen Exchanger 3Sodium-Hydrogen Exchangers

Identifiers

PMID21148403
PMCPMC3063980
OpenAlexW2157476765

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.