Evidence map›Paper›PMID 19955190›Full record

ArticleAmerican journal of physiology. Renal physiology2010

Characterization of vasopressin-responsive collecting duct adenylyl cyclases in the mouse.

Kevin A Strait, Peter K Stricklett, Mark Chapman, Donald E Kohan

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

31 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Stimulation of the Epithelial NaFrontiers in physiology · 2021
    Article
  6. Review
  7. Renomedullary Interstitial Cell Endothelin A Receptors Regulate BP and Renal Function.Journal of the American Society of Nephrology : JASN · 2020
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. PGEAmerican journal of physiology. Renal physiology · 2017
    Article
  14. STIM1fl/fl Ksp-Cre Mouse has Impaired Renal Water Balance.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2016
    Article
  15. Glycogen synthase kinase 3α regulates urine concentrating mechanism in mice.American journal of physiology. Renal physiology · 2015
    Article
  16. Tolvaptan plus pasireotide shows enhanced efficacy in a PKD1 model.Journal of the American Society of Nephrology : JASN · 2015
    Article
  17. Article
  18. Article
  19. Regulation of nephron water and electrolyte transport by adenylyl cyclases.American journal of physiology. Renal physiology · 2014
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Kevin A StraitDivision of Nephrology, University of Utah Health Sciences Center, 1900 East 30 North, Salt Lake City, UT 84132, USA.
Peter K Stricklett
Mark Chapman
Donald E Kohan
University of Utah · US

Funding

NIDDK NIH HHS DK-96392
6 · The paper itself

Abstract

Little is known about collecting duct adenylyl cyclase (AC) isoforms or regulation in the mouse. We performed RT-PCR for AC isoforms 1-9 in microdissected cortical (CCD) and outer medullary (OMCD) and acutely isolated inner medullary (IMCD) collecting duct. All collecting duct regions contained AC3, AC4, and AC6 mRNA, while CCD and OMCD, but not IMCD, also contained AC5 mRNA. Acutely isolated IMCD expressed AC3, AC4, and AC6 proteins by Western blot analysis. The mIMCD3 cell line expressed AC2, AC3, AC4, AC5, and AC6 mRNA; M-1 CCD cells expressed AC2, 3, 4, and 6, while mpkCCD cell lines contained AC3, AC4, and AC6 mRNA. AVP stimulated cAMP accumulation in acutely isolated mouse IMCD; this was reduced by chelation of extracellular calcium (EGTA) and almost completely abolished by blockade of calmodulin (W-7). Blockade of calmodulin kinase with KN-93 or endoplasmic reticulum calcium ATPase (thapsigargin) also reduced the AVP response. A similar inhibitory effect of W-7, KN-93, and thapsigargin was seen on forskolin-stimulated cAMP content in acutely isolated mouse IMCD. These three agents had the same pattern of blockade of AVP- or forskolin-stimulated AC activity in acutely isolated rat IMCD. AVP responsiveness in primary cultures of mouse IMCD was also reduced by W-7, KN-93, and thapsigargin. Small interfering RNA (siRNA) designed to knock down AC3 or AC6 in primary cultured mouse IMCD significantly reduced AVP-stimulated cAMP accumulation. Together, these data are consistent with a role of AC3 and AC6 in the activation of mouse collecting duct by AVP.

Indexed as

Adenylyl CyclasesAnimalsAntidiuretic AgentsBlotting, WesternCell LineCyclic AMPGene Expression Regulation, EnzymologicIsoenzymesKidney Tubules, CollectingMiceMice, Inbred C57BLRatsRats, Sprague-DawleyReverse Transcriptase Polymerase Chain ReactionRNA InterferenceRNA, Small InterferingAdenylyl CyclasesAntidiuretic AgentsCyclic AMPIsoenzymesRNA, Small InterferingVasopressins

Identifiers

PMID19955190
PMCPMC2853316
OpenAlexW2137061543

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.