Evidence map›Paper›PMID 7593604›Full record

ArticleThe Journal of clinical investigation1995

Activation of protein kinase A acutely inhibits and phosphorylates Na/H exchanger NHE-3.

O W Moe, M Amemiya, Y Yamaji

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 93 citations in OpenAlex.

  1. NaInternational journal of molecular sciences · 2023
    Review
  2. Identification of a Primary Renal ATCirculation research · 2020
    Article
  3. Article
  4. Defective Renal Angiotensin III and ATJournal of the American Heart Association · 2019
    Article
  5. Article
  6. Review
  7. Na+/H+ and Na+/NH+4 activities of zebrafish NHE3b expressed in Xenopus oocytes.American journal of physiology. Regulatory, integrative and comparative physiology · 2014
    Article
  8. Article
  9. Article
  10. Article
  11. Luminal Na(+)/H (+) exchange in the proximal tubule.Pflugers Archiv : European journal of physiology · 2009
    Review
  12. Regulation of sodium pump endocytosis by cardiotonic steroids: Molecular mechanisms and physiological implications.Pathophysiology : the official journal of the International Society for Pathophysiology · 2007
    Article
  13. Review
  14. NHERF and regulation of the renal sodium-hydrogen exchanger NHE3.Pflugers Archiv : European journal of physiology · 2005
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. cAMP-mediated inhibition of the epithelial brush border Na+/H+ exchanger, NHE3, requires an associated regulatory protein.Proceedings of the National Academy of Sciences of the United States of America · 1997
    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

3 authors at 2 institutions in 2 countries.

O W MoeDepartment of Internal Medicine, Department of Veterans Affairs, Dallas, Texas, USA.
M Amemiya
Y Yamaji
The University of Texas Southwestern Medical Center · USDepartment of Veterans Affairs · AU

Funding

Acute Regulation of the Renal Na/H Exchanger NHE-3R01DK048482 · NIDDK · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI MOE, ORSON W · 2001 to 2005
$1.3M
REGULATION OF RENAL NA+/H+ EXCHANGER BY PROTEIN KINASE AR29DK048482 · NIDDK · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI MOE, ORSON W · 1995 to 1999
–
NIDDK NIH HHS DK48482-01
6 · The paper itself

Abstract

In the mammalian renal proximal tubule, protein kinase A (PKA) plays an important role in mediating hormonal regulation of apical membrane Na/H exchanger activity. This exchanger is likely encoded by NHE-3. The present studies examined regulation of NHE-3 by PKA. NHE-3 was stably expressed in Na/H exchanger-deficient fibroblasts (AP-1/NHE-3 cells). PKA activation (0.1 mM 8-BrcAMP x 20 min) inhibited NHE-3 activity by 39% (P < 0.01) with no change in NHE-3 protein abundance in the plasma membrane. To define the structural requirements for PKA-mediated inhibition, full-length NHE-3 and a cytoplasmic domain-truncated mutant (NHE-3 delta cyto) were expressed in Xenopus laevis oocytes. 8-BrcAMP inhibited NHE-3 activity by 27% (P < 0.05), an effect that was blocked by 10(-7) M PKA inhibitor peptide. NHE-3 delta cyto had baseline activity similar to that of full-length NHE-3 but its activity was not regulated by 8-BrcAMP. The purified recombinant cytoplasmic domain of NHE-3 was phosphorylated in vitro by the catalytic subunit of PKA on serine residues. In AP-1/NHE-3 cells, NHE-3 was immunoprecipitated as a approximately 87-kD phosphoprotein. Addition of 0.1 mM 8-BrcAMP increased the phosphocontent of NHE-3 by threefold. In summary, acute activation of PKA inhibits NHE-3 activity, an effect that is likely mediated by phosphorylation of its cytoplasmic domain.

Indexed as

Amino Acid SequenceAnimalsBiological TransportCHO CellsCricetinaeCyclic AMP-Dependent Protein KinasesEnzyme ActivationFemaleGene ExpressionMolecular Sequence DataPhosphorylationRNA, MessengerSodium-Hydrogen ExchangersXenopus laevisCyclic AMP-Dependent Protein KinasesRNA, MessengerSodium-Hydrogen Exchangers

Identifiers

PMID7593604
PMCPMC185868
OpenAlexW2004104084

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.