Evidence map›Paper›PMID 23739593›Full record

ArticleAmerican journal of physiology. Renal physiology2013

Aldosterone acutely stimulates NCC activity via a SPAK-mediated pathway.

Benjamin Ko, Abinash C Mistry, Lauren Hanson, Rickta Mallick, Brandi M Wynne, Tiffany L Thai, James L Bailey, Janet D Klein, Robert S Hoover

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

32 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Kidney-specific KO of the circadian clock protein PER1 alters renal NaAmerican journal of physiology. Renal physiology · 2022
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. NBCe1-A is required for the renal ammonia and KAmerican journal of physiology. Renal physiology · 2020
    Article
  13. Hyperkalemia: pathophysiology, risk factors and consequences.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2019
    Review
  14. Article
  15. Review
  16. Severe hyperkalemia is rescued by low-potassium diet in renal βENaC-deficient mice.Pflugers Archiv : European journal of physiology · 2017
    Article
  17. (Pro)Renin receptor regulates potassium homeostasis through a local mechanism.American journal of physiology. Renal physiology · 2017
    Article
  18. Article
  19. Article
  20. Serum and Glucocorticoid Regulated Kinase 1 in Sodium Homeostasis.International journal of molecular sciences · 2016
    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

9 authors at 2 institutions in 1 country.

Benjamin KoDepartment of Medicine, University of Chicago, Chicago, Illinois, USA. bko@uchicago.edu
Abinash C Mistry
Lauren Hanson
Rickta Mallick
Brandi M Wynne
Tiffany L Thai
James L Bailey
Janet D Klein
Robert S Hoover
Emory University · USUniversity of Chicago · US

Funding

Regulation of Renal Inner Medullary FunctionR01DK041707 · NIDDK · EMORY UNIVERSITY · PI SANDS, JEFF M · 1996 to 2017
$4.3M
Nephrology Institutional Training Grant FLSA SupplementT32DK007656 · NIDDK · EMORY UNIVERSITY · PI SANDS, JEFF M, WALL, SUSAN MARIE · 1990 to 2020
$3.5M
Mechanisms of Hormonal Regulation of the Sodium Chloride CotransporterR01DK085097 · NIDDK · EMORY UNIVERSITY · PI HOOVER, ROBERT S · 2010 to 2015
$1.5M
The Role of Ubiquitin in Sodium Chloride Co-Transporter RegulationK08DK081728 · NIDDK · UNIVERSITY OF CHICAGO · PI KO, BENJAMIN S · 2008 to 2012
$691k
NIDDK NIH HHS K08 DK081728NIDDK NIH HHS R01 DK-085097NIDDK NIH HHS R01 DK085097NIDDK NIH HHS R01 DK41707NIDDK NIH HHS T32 DK007656NIDDK NIH HHS T32 DK07656
6 · The paper itself

Abstract

Hypertension is a leading cause of morbidity and mortality worldwide, and disordered sodium balance has long been implicated in its pathogenesis. Aldosterone is perhaps the key regulator of sodium balance and thus blood pressure. The sodium chloride cotransporter (NCC) in the distal convoluted tubule of the kidney is a major site of sodium reabsorption and plays a key role in blood pressure regulation. Chronic exposure to aldosterone increases NCC protein expression and function. However, more acute effects of aldosterone on NCC are unknown. In our salt-abundant modern society where chronic salt deprivation is rare, understanding the acute effects of aldosterone is critical. Here, we examined the acute effects (12-36 h) of aldosterone on NCC in the rodent kidney and in a mouse distal convoluted tubule cell line. Studies demonstrated that aldosterone acutely stimulated NCC activity and phosphorylation without affecting total NCC abundance or surface expression. This effect was dependent upon the presence of the mineralocorticoid receptor and serum- and glucocorticoid-regulated kinase 1 (SGK1). Furthermore, STE20/SPS-1-related proline/alanine-rich kinase (SPAK) phosphorylation also increased, and gene silencing of SPAK eliminated the effect of aldosterone on NCC activity. Aldosterone administration via a minipump in adrenalectomized rodents confirmed an increase in NCC phosphorylation without a change in NCC total protein. These data indicate that acute aldosterone-induced SPAK-dependent phosphorylation of NCC increases individual transporter activity.

Indexed as

AdrenalectomyAldosteroneAnimalsCells, CulturedImmediate-Early ProteinsMaleMicePhosphorylationProtein Serine-Threonine KinasesRatsRats, Sprague-DawleyReceptors, MineralocorticoidSerum-Glucocorticoid Regulated KinasesSodium Chloride SymportersSolute Carrier Family 12, Member 3AldosteroneImmediate-Early ProteinsPAS domain kinasesProtein Serine-Threonine KinasesReceptors, MineralocorticoidSerum-Glucocorticoid Regulated KinasesSlc12a3 protein, mouseSodium Chloride SymportersSolute Carrier Family 12, Member 3aldosteroneNCCSPAKWNK4

Identifiers

PMID23739593
PMCPMC3761211
OpenAlexW2139600905

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.