Evidence map›Paper›PMID 22170617›Full record

ReviewAmerican journal of physiology. Regulatory, integrative and comparative physiology2012

Lessons from in vitro studies and a related intracellular angiotensin II transgenic mouse model.

Julia L Cook, Richard N Re

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Regulatory, integrative and comparative physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Intracrine angiotensin II functions originate from noncanonical pathways in the human heart.American journal of physiology. Heart and circulatory physiology · 2016
    Review
  12. Biochemical evaluation of the renin-angiotensin system: the good, bad, and absolute?American journal of physiology. Heart and circulatory physiology · 2016
    Review
  13. Review
  14. Article
  15. Review
  16. The ins and outs of angiotensin processing within the kidney.American journal of physiology. Regulatory, integrative and comparative physiology · 2014
    Review
  17. Review
  18. Direct evidence of intracrine angiotensin II signaling in neurons.American journal of physiology. Cell physiology · 2014
    Article
  19. Article
  20. Thirty years of intracrinology.Ochsner journal · 2014
    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

2 authors at 2 institutions in 2 countries.

Julia L CookLaboratory of Molecular Genetics, Department of Research, New Orleans, LA 70121, USA. jcook@ochsner.org
Richard N Re
Laboratory of Molecular Genetics · PLOchsner Medical Center · US

Funding

Effects of intracellular angiotensin IIR01HL072795 · NHLBI · OCHSNER CLINIC FOUNDATION · PI COOK, JULIA L · 2005 to 2009
$1.7M
NHLBI NIH HHS HL-072795NHLBI NIH HHS R01 HL072795
6 · The paper itself

Abstract

In the classical renin-angiotensin system, circulating ANG II mediates growth stimulatory and hemodynamic effects through the plasma membrane ANG II type I receptor, AT1. ANG II also exists in the intracellular space in some native cells, and tissues and can be upregulated in diseases, including hypertension and diabetes. Moreover, intracellular AT1 receptors can be found associated with endosomes, nuclei, and mitochondria. Intracellular ANG II can function in a canonical fashion through the native receptor and also in a noncanonical fashion through interaction with alternative proteins. Likewise, the receptor and proteolytic fragments of the receptor can function independently of ANG II. Participation of the receptor and ligand in alternative intracellular pathways may serve to amplify events that are initiated at the plasma membrane. We review historical and current literature relevant to ANG II, compared with other intracrines, in tissue culture and transgenic models. In particular, we describe a new transgenic mouse model, which demonstrates that intracellular ANG II is linked to high blood pressure. Appreciation of the diverse, pleiotropic intracellular effects of components of the renin-angiotensin system should lead to alternative disease treatment targets and new therapies.

Indexed as

Angiotensin IIAnimalsCell NucleusCytoplasmDisease Models, AnimalHypertensionIn Vitro TechniquesMiceMice, TransgenicReceptor, Angiotensin, Type 1Renin-Angiotensin SystemAngiotensin IIReceptor, Angiotensin, Type 1

Identifiers

PMID22170617
PMCPMC3311520
OpenAlexW2040458141

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.