Evidence map›Paper›PMID 26159698›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2015

Sodium butyrate stimulates NHE8 expression via its role on activating NHE8 basal promoter activity.

Hua Xu, Anthony McCoy, Jing Li, Yang Zhao, Fayez K Ghishan

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Nutrients · 2022
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Pathophysiology of Intestinal NaCellular and molecular gastroenterology and hepatology · 2017
    Article
  8. Review
  9. Article
  10. Intestinal NHE8 is highly expressed in goblet cells and its expression is subject to TNF-α regulation.American journal of physiology. Gastrointestinal and liver physiology · 2016
    Article
  11. Protein-DNA Interactions at the Opossum Npt2a Promoter are Dependent upon NHERF-1.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2016
    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

5 authors at 1 institution in 1 country.

Hua XuUniversity of Arizona, Tucson, Arizona.
Anthony McCoyUniversity of Arizona, Tucson, Arizona.
Jing LiUniversity of Arizona, Tucson, Arizona.
Yang ZhaoUniversity of Arizona, Tucson, Arizona.
Fayez K GhishanUniversity of Arizona, Tucson, Arizona fghishan@peds.arizona.edu.
University of Arizona · US

Funding

Regulation of a Novel Intestinal NHE Isoform (NHE8)R01DK073638 · NIDDK · UNIVERSITY OF ARIZONA · PI GHISHAN, FAYEZ KHALAF · 2006 to 2015
$3.1M
NIDDK NIH HHS R01 DK073638NIDDK NIH HHS R01-DK-073638
6 · The paper itself

Abstract

Butyrate is a major metabolite in colonic lumen. It is produced from bacterial fermentation of dietary fiber. Butyrate has been shown to stimulate electroneutral sodium absorption through its regulation on sodium/hydrogen exchanger 3 (NHE3). Although NHE8, the newest addition of intestinal NHE family, is involved in sodium absorption in the intestinal tract, whether butyrate modulates NHE8 expression in the intestinal epithelial cells is not known. In the current study, we showed that butyrate treatment strongly induced NHE8 protein and NHE8 mRNA expression in human intestinal epithelial cells. Transfection with the human NHE8 promoter reporter constructs showed that butyrate treatment stimulated reporter gene expression at an amount comparable with its stimulation of NHE8 mRNA expression. Interestingly, a similar result was also observed in human NHE8 promoter transfected cells after trichostatin (TSA) treatment. Gel mobility shift assay identified an enhanced Sp3 protein binding on the human NHE8 basal promoter region upon butyrate stimulation. Furthermore, Sp3 acetylation modification is involved in butyrate-mediated NHE8 activation in Caco-2 cells. Our findings suggest that the mechanism of butyrate action on NHE8 expression involves enhanced Sp3 interaction at the basal promoter region of the human NHE8 gene promoter to activate NHE8 gene transcription. Thus butyrate is involved in intestinal regulation of NHE8 resulting enhanced sodium absorption.

Indexed as

AcetylationButyric AcidCaco-2 CellsGene Expression RegulationGenes, ReporterHumansPromoter Regions, GeneticRNA, MessengerSodium-Hydrogen ExchangersSp3 Transcription FactorButyric AcidRNA, MessengerSLC9A8 protein, humanSodium-Hydrogen ExchangersSP3 protein, humanSp3 Transcription FactoracetylationbutyrateintestineNHE8Sp3

Identifiers

PMID26159698
PMCPMC4572406
OpenAlexW2164787408

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.