Evidence map›Paper›PMID 22193384›Full record

ArticleJournal of the American Society of Nephrology : JASN2012

Binding of losartan to angiotensin AT1 receptors increases dopamine D1 receptor activation.

Dong Li, Lena Scott, Susanne Crambert, Sergey Zelenin, Ann-Christine Eklöf, Luis Di Ciano, Fernando Ibarra, Anita Aperia

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Role of G-Proteins and GPCRs in Cardiovascular Pathologies.Bioengineering (Basel, Switzerland) · 2023
    Review
  9. Review
  10. Review
  11. Role of the central renin‑angiotensin system in hypertension (Review).International journal of molecular medicine · 2021
    Review
  12. Article
  13. Review
  14. Brain Renin-Angiotensin System Blockade Attenuates Methamphetamine-Induced Hyperlocomotion and Neurotoxicity.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Article
  15. ATBMC cardiovascular disorders · 2017
    Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Regulation of blood pressure, oxidative stress and AT1R by high salt diet in mutant human dopamine D5 receptor transgenic mice.Hypertension research : official journal of the Japanese Society of Hypertension · 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

8 authors at 3 institutions in 2 countries.

Dong LiDepartment of Women's and Children's Health, Karolinska University Hospital, Q2:09, S-171 76 Stockholm, Sweden.
Lena Scott
Susanne Crambert
Sergey Zelenin
Ann-Christine Eklöf
Luis Di Ciano
Fernando Ibarra
Anita Aperia
Karolinska Institutet · SEInstituto de Diagnóstico e Investigaciones Metabólicas · ARUniversity of Buenos Aires · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Signaling through both angiotensin AT1 receptors (AT1R) and dopamine D1 receptors (D1R) modulates renal sodium excretion and arterial BP. AT1R and D1R form heterodimers, but whether treatment with AT1R antagonists functionally modifies D1R via allosterism is unknown. In this study, the AT1R antagonist losartan strengthened the interaction between AT1R and D1R and increased expression of D1R on the plasma membrane in vitro. In rat proximal tubule cells that express endogenous AT1R and D1R, losartan increased cAMP generation. Losartan increased cAMP in HEK 293a cells transfected with both AT1R and D1R, but it did not increase cAMP in cells transfected with either receptor alone, suggesting that losartan induces D1R activation. Furthermore, losartan did not increase cAMP in HEK 293a cells expressing AT1R and mutant S397/S398A D1R, which disrupts the physical interaction between AT1R and D1R. In vivo, administration of a D1R antagonist significantly attenuated the antihypertensive effect of losartan in rats with renal hypertension. Taken together, these data imply that losartan might exert its antihypertensive effect both by inhibiting AT1R signaling and by enhancing D1R signaling.

Indexed as

Angiotensin II Type 1 Receptor BlockersAnimalsAortic CoarctationBenzazepinesCell MembraneCyclic AMPDisease Models, AnimalHEK293 CellsHumansHypertensionIn Vitro TechniquesKidneyKidney Tubules, ProximalLosartanMaleProtein BindingAngiotensin II Type 1 Receptor BlockersBenzazepinesCyclic AMPLosartanReceptor, Angiotensin, Type 1Receptors, Dopamine D1SCH 23390

Identifiers

PMID22193384
PMCPMC3294303
OpenAlexW2116490811

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.