Evidence map›Paper›PMID 8698857›Full record

ArticleThe Journal of clinical investigation1996

Expression of type II cGMP-dependent protein kinase in rat kidney is regulated by dehydration and correlated with renin gene expression.

S Gambaryan, C Häusler, T Markert, D Pöhler, T Jarchau, U Walter, W Haase, A Kurtz, S M Lohmann

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
  2. cGMP-dependent protein kinase I in vascular smooth muscle cells improves ischemic stroke outcome in mice.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2019
    Article
  3. Article
  4. Article
  5. Article
  6. Function of cGMP-dependent protein kinase II in volume load-induced diuresis.Pflugers Archiv : European journal of physiology · 2014
    Article
  7. Review
  8. Article
  9. ENaC is regulated by natriuretic peptide receptor-dependent cGMP signaling.American journal of physiology. Renal physiology · 2013
    Article
  10. Regulation of renin secretion by renal juxtaglomerular cells.Pflugers Archiv : European journal of physiology · 2013
    Review
  11. Article
  12. Article
  13. Megakaryocyte hyperplasia and enhanced agonist-induced platelet activation in vasodilator-stimulated phosphoprotein knockout mice.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  14. Article
  15. Article
  16. Article
  17. 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

9 authors at 3 institutions in 2 countries.

S GambaryanMedizinische Universitäts-Klinik, Klinische Biochemie and Pathobiochemie, Würzburg, Germany.
C Häusler
T Markert
D Pöhler
T Jarchau
U Walter
W Haase
A Kurtz
S M Lohmann
Research Institute of Inorganic Chemistry · CZMax Planck Institute of Biophysics · DEUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

cGMP-based regulatory systems are vital for counteracting the renin-angiotensin system (RAS) which promotes volume expansion and high blood pressure. Natriuretic peptides and nitric oxide acting through their second messenger cGMP normally increase natriuresis and diuresis, and regulate renin release; however, the severe pathological state of cardiac heart failure is characterized by elevated levels of atrial natriuretic peptide that are no longer able to effectively oppose exaggerated RAS effects. There is presently limited information on the intracellular effectors of cGMP actions in the kidney. Recently we reported the cloning of the cDNA for type II cGMP-dependent protein kinase (cGK II), which is highly enriched in intestinal mucosa but was also detected for the first time in kidney. In the present study, cGK II was localized to juxtaglomerular (JG) cells, the ascending thin limb (ATL), and to a lesser extent the brush border of proximal tubules. An activator of renin gene expression, the angiotensin II type I receptor inhibitor, losartan, increased cGK II mRNA and protein three to fourfold in JG cells. In other experiments, water deprivation increased cGK II mRNA and protein three to fourfold in the inner medulla where both cGK II, and a kidney specific CI- channel shown by others to be regulated by dehydration, are localized in the ATL. Whereas additional data suggest that cGK I may primarily mediate cGMP-related changes in renal hemodynamics, cGK II may regulate renin release and ATL ion transport.

Indexed as

Gene Expression Regulation, EnzymologicAnimalsAtrial Natriuretic FactorBase SequenceBiphenyl CompoundsChloridesCyclic GMP-Dependent Protein KinasesDehydrationImidazolesIsoenzymesKidneyLosartanMaleMolecular Sequence DataRatsRats, Sprague-DawleyAtrial Natriuretic FactorBiphenyl CompoundsChloridesCyclic GMP-Dependent Protein KinasesImidazolesIsoenzymesLosartanReninRNA, MessengerTetrazoles

Identifiers

PMID8698857
PMCPMC507475
OpenAlexW2057641167

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.