Evidence map›Paper›PMID 25377912›Full record

ArticleAmerican journal of physiology. Renal physiology2015

Renal NHE expression and activity in neonatal NHE3- and NHE8-null mice.

Kwanchai Pirojsakul, Jyothsna Gattineni, Vangipuram Dwarakanath, Michel Baum

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

4 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. The Physiological Function and Potential Role of the Ubiquitous NaInternational journal of molecular sciences · 2022
    Review
  3. Article
  4. 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

4 authors at 1 institution in 1 country.

Kwanchai PirojsakulDepartment of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas; and.
Jyothsna GattineniDepartment of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas; and.
Vangipuram DwarakanathDepartment of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas; and.
Michel BaumDepartment of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas; and Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas Michel.Baum@UTSouthwestern.edu.
The University of Texas Southwestern Medical Center · US

Funding

UT Southwestern O'Brien Kidney Research Core CenterP30DK079328 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI MOE, ORSON W · 2007 to 2021
$16.9M
Neonatal Proximal Tubule AcidificationR01DK041612 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI BAUM, MICHEL GERARD, MOE, ORSON W · 1991 to 2013
$2.7M
Effect of Prenatal Programming on Renal Tubular TransportR01DK078596 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI BAUM, MICHEL GERARD · 2009 to 2012
$1.3M
NIDDK NIH HHS DK078596NIDDK NIH HHS DK41612NIDDK NIH HHS P30 DK079328NIDDK NIH HHS P30DK079328PHS HHS NIDDK 100000062
6 · The paper itself

Abstract

Na(+)/H(+) exchanger (NHE)3 is the predominant NHE on the brush-border membrane of the proximal tubule in adult animals. NHE8 has been localized to the brush-border membrane of proximal tubules and is more highly expressed in neonates than in adult animals. However, the relative role of NHE8 in neonatal renal acidification is unclear. The present study examined if there was a compensatory increase in NHE3 in NHE8-null neonatal mice and whether there was a compensatory increase in NHE8 in NHE3-null neonatal mice. In addition, we examined whether wild-type, NHE3-null, and NHE8-null mice had an increase in NHE activity in response to metabolic acidosis. We found that at baseline, there was comparable renal NHE3 mRNA, total protein, and brush-border membrane protein abundance as in neonatal control and NHE8-null mice. There was comparable renal NHE8 mRNA, total protein, and brush-border membrane protein abundance in NHE3-null neonatal and control mice. Both NHE3- and NHE8-null mice had a comparable but lower rate of NHE activity than control mice. We next imposed metabolic acidosis in wild-type, NHE3-null, and NHE8-null mice. Acidemic NHE8-null mice had an increase in brush-border membrane vesicle NHE3 protein abundance and NHE activity compared with vehicle-treated mice. Likewise, NHE3-null mice had an increase in NHE8 brush-border membrane protein abundance and NHE activity in response to metabolic acidosis. In conclusion, both NHE3 and NHE8 likely play a role in neonatal acidification.

Indexed as

AnimalsAnimals, NewbornFemaleKidneyMaleMice, Inbred C57BLMicrovilliSodium-Hydrogen Exchanger 3Sodium-Hydrogen ExchangersSlc9a3 protein, mouseSlc9a8 protein, mouseSodium-Hydrogen Exchanger 3Sodium-Hydrogen Exchangersacidosisdevelopmentproximal tubulesodium/hydrogen exchanger

Identifiers

PMID25377912
PMCPMC4281693
OpenAlexW1995289299

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.