Evidence map›Paper›PMID 19692483›Full record

ArticleAmerican journal of physiology. Renal physiology2009

Activation of the epithelial Na+ channel in the collecting duct by vasopressin contributes to water reabsorption.

Vladislav Bugaj, Oleh Pochynyuk, James D Stockand

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

52 citing papers in PubMed, 84 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Ovarian hormones moderate systolic hypertension in femaleAmerican journal of physiology. Renal physiology · 2026
    Article
  5. Ovarian Hormones Moderate Systolic Hypertension in FemalebioRxiv : the preprint server for biology · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Stimulation of the Epithelial NaFrontiers in physiology · 2021
    Article
  12. Article
  13. A peek into Epac physiology in the kidney.American journal of physiology. Renal physiology · 2019
    Article
  14. Article
  15. Review
  16. EHD4 is a novel regulator of urinary water homeostasis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  17. Article
  18. Involvement of ENaC in the development of salt-sensitive hypertension.American journal of physiology. Renal physiology · 2017
    Review
  19. Alveolar nonselective channels are ASIC1a/α-ENaC channels and contribute to AFC.American journal of physiology. Lung cellular and molecular physiology · 2017
    Article
  20. 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 1 institution in 1 country.

Vladislav BugajDepartment of Physiology, University of Texas Health Science Center, San Antonio, Texas 78229-3900, USA.
Oleh Pochynyuk
James D Stockand
The University of Texas Health Science Center at San Antonio · US

Funding

Regulation of the epithelial Na+ channel by Ras and SgkR01DK059594 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI STOCKAND, JAMES D · 2002 to 2012
$2.7M
NIDDK NIH HHS R01-DK-059594
6 · The paper itself

Abstract

We used patch-clamp electrophysiology on isolated, split-open murine collecting ducts (CD) to test the hypothesis that regulation of epithelial sodium channel (ENaC) activity is a physiologically important effect of vasopressin. Surprisingly, this has not been tested directly before. We ask whether vasopressin affects ENaC activity distinguishing between acute and chronic effects, as well as, parsing the cellular signaling pathway and molecular mechanism of regulation. In addition, we quantified possible synergistic regulation of ENaC by vasopressin and aldosterone associating this with a requirement for distal nephron Na+ reabsorption during water conservation vs. maintenance of Na+ balance. We find that vasopressin significantly increases ENaC activity within 2-3 min by increasing open probability (P(o)). This activation was dependent on adenylyl cyclase (AC) and PKA. Water restriction (18-24 h) and pretreatment of isolated CD with vasopressin (approximately 30 min) resulted in a similar increase in P(o). In addition, this also increased the number (N) of active ENaC in the apical membrane. Similar to P(o), increases in N were sensitive to inhibitors of AC. Stressing animals with water and salt restriction separately and jointly revealed an important effect of vasopressin: conservation of water and Na+ each independently increased ENaC activity and jointly had a synergistic effect on channel activity. These results demonstrate a quantitatively important action of vasopressin on ENaC suggesting that distal nephron Na+ reabsorption mediated by this channel contributes to maintenance of water reabsorption. In addition, our results support that the combined actions of vasopressin and aldosterone are required to achieve maximally activated ENaC.

Indexed as

Epithelial Sodium Channel AgonistsAbsorptionAdenylyl Cyclase InhibitorsAdenylyl CyclasesAldosteroneAnimalsArginine VasopressinCyclic AMP-Dependent Protein KinasesElectrophysiologyEpithelial Sodium ChannelsFemaleKidney Tubules, CollectingMaleMicePatch-Clamp TechniquesRenal AgentsAdenylyl Cyclase InhibitorsAdenylyl CyclasesAldosteroneArginine VasopressinCyclic AMP-Dependent Protein KinasesEpithelial Sodium Channel AgonistsEpithelial Sodium ChannelsRenal AgentsSodiumVasopressinsWater

Identifiers

PMID19692483
PMCPMC2781343
OpenAlexW2032226073

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.