Evidence map›Paper›PMID 9109429›Full record

ArticleThe Journal of clinical investigation1997

Role of renal aquaporins in escape from vasopressin-induced antidiuresis in rat.

C A Ecelbarger, S Nielsen, B R Olson, T Murase, E A Baker, M A Knepper, J G Verbalis

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

51 citing papers in PubMed, 228 citations in OpenAlex.

  1. Trial
  2. Proteomics and AQP2 regulation.The Journal of physiology · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Soluble (pro)renin receptor as a potential therapy for diabetes insipidus.American journal of physiology. Renal physiology · 2018
    Review
  12. Genome-Wide Mapping of DNA Accessibility and Binding Sites for CREB and C/EBPJournal of the American Society of Nephrology : JASN · 2018
    Article
  13. Article
  14. Article
  15. Diagnosis and Treatment of Hyponatremia: Compilation of the Guidelines.Journal of the American Society of Nephrology : JASN · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Disruption of prostaglandin E2 receptor EP4 impairs urinary concentration via decreasing aquaporin 2 in renal collecting ducts.Proceedings of the National Academy of Sciences of the United States of America · 2015
    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

7 authors at 5 institutions in 2 countries.

C A EcelbargerLaboratory of Kidney and Electrolyte Metabolism, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
S Nielsen
B R Olson
T Murase
E A Baker
M A Knepper
J G Verbalis
Georgetown University · USAalborg University · DKNational Heart Lung and Blood Institute · USNational Institutes of Health · USWaterbury Hospital · US

Funding

PHYSIOLOGICAL ADAPTATION TO SUSTAINED HYPO-OSOMOLALITYR01DK038094 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VERBALIS, JOSEPH G · 1988 to 2002
$451k
NIDDK NIH HHS DK-38094
6 · The paper itself

Abstract

The purpose of this study was to investigate whether escape from vasopressin-induced antidiuresis is associated with altered regulation of any of the known aquaporin water channels. After 4-d pretreatment with 1-deamino-[8-D-arginine]-vasopressin (dDAVP) by osmotic mini-pump, rats were divided into two groups: control (continued dDAVP) and water-loaded (continued dDAVP plus a daily oral water load). A significant increase in urine volume in the water-loaded rats was observed by the second day of water loading, indicating onset of vasopressin escape. The onset of escape coincided temporally with a marked decrease in renal aquaporin-2 protein (measured by semiquantitative immunoblotting), which began at day 2 and fell to 17% of control levels by day 3. In contrast, there was no decrease in the renal expression of aquaporins 1, 3, or 4. The marked suppression of whole kidney aquaporin-2 protein was accompanied by a concomitant suppression of whole kidney aquaporin-2 mRNA levels. Immunocytochemical localization and differential centrifugation studies demonstrated that trafficking of aquaporin-2 to the plasma membrane remained intact during vasopressin escape. The results suggest that escape from vasopressin-induced antidiuresis is attributable, at least in part, to a vasopressin-independent decrease in aquaporin-2 water channel expression in the renal collecting duct.

Indexed as

AquaporinsAnimalsAquaporin 2Aquaporin 3Aquaporin 6Base SequenceCell Membrane PermeabilityDeamino Arginine VasopressinDiuresisDNA PrimersIon ChannelsKidneyKidney Tubules, CollectingKineticsMaleRatsAqp2 protein, ratAqp3 protein, ratAquaporin 2Aquaporin 3Aquaporin 6AquaporinsDeamino Arginine VasopressinDNA PrimersIon ChannelsRenal AgentsRNA, MessengerWater

Identifiers

PMID9109429
PMCPMC508009
OpenAlexW1994266582

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.