Evidence map›Paper›PMID 26608789›Full record

ArticleAmerican journal of physiology. Renal physiology2016

Vasopressin/V2 receptor stimulates renin synthesis in the collecting duct.

Alexis A Gonzalez, Flavia Cifuentes-Araneda, Cristobal Ibaceta-Gonzalez, Alex Gonzalez-Vergara, Leonardo Zamora, Ricardo Henriquez, Carla B Rosales, L Gabriel Navar, Minolfa C Prieto

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2016. 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
2.8field-weighted citation impact, top 9% 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, 32 citations in OpenAlex.

  1. Effect of Pituitary-Target Gland Axis on RAAS in the Context of COVID-19.International journal of medical sciences · 2025
    Review
  2. Review
  3. Review
  4. Article
  5. Complementary Role of Oxytocin and Vasopressin in Cardiovascular Regulation.International journal of molecular sciences · 2021
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Soluble (pro)renin receptor as a potential therapy for diabetes insipidus.American journal of physiology. Renal physiology · 2018
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. PGEAmerican journal of physiology. Renal physiology · 2017
    Article
  16. Prostaglandin EThe American journal of the medical sciences · 2017
    Article
  17. Review
  18. Bradykinin/BPhysiological reports · 2017
    Article
  19. Review
  20. 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 2 countries.

Alexis A GonzalezInstituto de Química, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile; alexis.gonzalez@pucv.cl.
Flavia Cifuentes-AranedaInstituto de Química, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile;
Cristobal Ibaceta-GonzalezInstituto de Química, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile;
Alex Gonzalez-VergaraInstituto de Química, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile;
Leonardo ZamoraInstituto de Química, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile;
Ricardo HenriquezInstituto de Química, Pontificia Universidad Católica de Valparaíso, Valparaíso, Chile;
Carla B RosalesDepartment of Physiology Tulane University, School of Medicine, New Orleans, Louisiana; and.
L Gabriel NavarDepartment of Physiology Tulane University, School of Medicine, New Orleans, Louisiana; and Hypertension and Renal Center of Excellence, Tulane University, School of Medicine, New Orleans, Louisiana.
Minolfa C PrietoDepartment of Physiology Tulane University, School of Medicine, New Orleans, Louisiana; and Hypertension and Renal Center of Excellence, Tulane University, School of Medicine, New Orleans, Louisiana.
Pontificia Universidad Católica de Valparaíso · CLTulane University · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
Translational Research in Hypertension and Renal BiologyP30GM103337 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI NAVAR, LUIS GABRIEL · 2012 to 2016
$5.8M
PLEIOTROPIC EFFECTS OF PRORENIN RECEPOR IN COLLECTING DUCT AND INTRARENAL RAS ACTIVATIONR01DK104375 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI PRIETO, MINOLFA C · 2014 to 2018
$1.7M
NIDDK NIH HHS DK104375-01NIDDK NIH HHS R01 DK104375NIGMS NIH HHS P30 GM103337NIGMS NIH HHS P30GM-103337NIGMS NIH HHS U54 GM104940NIGMS NIH HHS U54-GM104940
6 · The paper itself

Abstract

Renin is synthesized in the principal cells of the collecting duct (CD), and its production is increased via cAMP in angiotensin (ANG) II-dependent hypertension, despite suppression of juxtaglomerular (JG) renin. Vasopressin, one of the effector hormones of the renin-angiotensin system (RAS) via the type 2-receptor (V2R), activates the cAMP/PKA/cAMP response element-binding protein (CREB) pathway and aquaporin-2 expression in principal cells of the CD. Accordingly, we hypothesized that activation of V2R increases renin synthesis via PKA/CREB, independently of ANG II type 1 (AT1) receptor activation in CD cells. Desmopressin (DDAVP; 10(-6) M), a selective V2R agonist, increased renin mRNA (∼3-fold), prorenin (∼1.5-fold), and renin (∼2-fold) in cell lysates and cell culture media in the M-1 CD cell line. Cotreatment with DDAVP+H89 (PKA inhibitor) or CREB short hairpin (sh) RNA prevented this response. H89 also blunted DDAVP-induced CREB phosphorylation and nuclear localization. In 48-h water-deprived (WD) mice, prorenin-renin protein levels were increased in the renal inner medulla (∼1.4- and 1.8-fold). In WD mice treated with an ACE inhibitor plus AT1 receptor blockade, renin mRNA and prorenin protein levels were still higher than controls, while renin protein content was not changed. In M-1 cells, ANG II or DDAVP increased prorenin-renin protein levels; however, there were no further increases by combined treatment. These results indicate that in the CD the activation of the V2R stimulates renin synthesis via the PKA/CREB pathway independently of RAS, suggesting a critical role for vasopressin in the regulation of renin in the CD.

Indexed as

Angiotensin-Converting Enzyme InhibitorsAngiotensin II Type 1 Receptor BlockersAnimalsCell LineCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteinDeamino Arginine VasopressinGene Knockdown TechniquesIsoquinolinesKidney MedullaKidney Tubules, CollectingMicePhosphorylationProtein Kinase InhibitorsReceptor, Angiotensin, Type 1Receptors, VasopressinAngiotensin-Converting Enzyme InhibitorsAngiotensin II Type 1 Receptor BlockersCreb1 protein, mouseCyclic AMP-Dependent Protein KinasesCyclic AMP Response Element-Binding ProteinDeamino Arginine VasopressinIsoquinolinesN-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamideProtein Kinase InhibitorsReceptor, Angiotensin, Type 1Receptors, VasopressinReninRNA, Small InterferingSulfonamidescollecting ductdistal tubular reninintrarenal renin-angiotensin systemPKA/CREBproreninwater deprivation

Identifiers

PMID26608789
PMCPMC4888561
OpenAlexW2180749458

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.