Evidence map›Paper›PMID 25527780›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2015

Caveolin-1 prevents sustained angiotensin II-induced resistance artery constriction and obesity-induced high blood pressure.

Istvan Czikora, Attila Feher, Rudolf Lucas, David J R Fulton, Zsolt Bagi

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2015. 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
0.9field-weighted citation impact, top 28% 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, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Orthogonal Peptide-Templated Labeling Elucidates Lateral ETChembiochem : a European journal of chemical biology · 2022
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  8. Review
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  10. Review
  11. Article
  12. Brain Renin-Angiotensin System Blockade Attenuates Methamphetamine-Induced Hyperlocomotion and Neurotoxicity.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Article
  13. Upregulation of ATFrontiers in physiology · 2018
    Article
  14. Article
  15. Article
  16. Review
  17. 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

5 authors at 1 institution in 1 country.

Istvan CzikoraVascular Biology Center, Medical College of Georgia, Georgia Regents University, Augusta, Georgia.
Attila FeherVascular Biology Center, Medical College of Georgia, Georgia Regents University, Augusta, Georgia.
Rudolf LucasVascular Biology Center, Medical College of Georgia, Georgia Regents University, Augusta, Georgia.
David J R FultonVascular Biology Center, Medical College of Georgia, Georgia Regents University, Augusta, Georgia.
Zsolt BagiVascular Biology Center, Medical College of Georgia, Georgia Regents University, Augusta, Georgia zbagi@gru.edu.
Augusta University · US

Funding

Metabolic Determinants of Cardiovascular Dysfunction in ObesityR01HL092446 · NHLBI · AUGUSTA UNIVERSITY · PI FULTON, DAVID J, STEPP, DAVID W · 2009 to 2013
$2.1M
Flow-induced coronary vasospasm in diabetic patientsR01HL104126 · NHLBI · NEW YORK MEDICAL COLLEGE · PI BAGI, ZSOLT · 2010 to 2014
$1.9M
NHLBI NIH HHS R01 HL-104126NHLBI NIH HHS R01 HL104126
6 · The paper itself

Abstract

The type 1 angiotensin II (ANG II) receptor (AT1R) undergoes internalization following stimulation by ANG II. Internalization reduces cell surface AT1Rs, and it is required for AT1R resensitization. In this process AT1R may interact with caveolin-1 (Cav1), the main scaffolding protein of caveolae. We hypothesized that the interaction between Cav1 and AT1R delays AT1R resensitization and thereby prevents sustained ANG II-induced resistance artery (RA) constriction under normal conditions and in experimental obesity. In rat and mouse skeletal muscle RA (diameter: ∼90-120 μm) ANG II-induced constrictions were reduced upon repeated (30-min apart) administrations. Upon disruption of caveolae with methyl-β-cyclodextrin or in RA of Cav1 knockout mice, repeated ANG II applications resulted in essentially maintained constrictions. In vascular smooth muscle cells, AT1R interacted with Cav1, and the degree of cell surface interactions was reduced by long-term (15-min), but not short-term (2-min), exposure to ANG II. When Cav1 was silenced, the amount of membrane-associated AT1R was significantly reduced by a short-term ANG II exposure. Moreover, Cav1 knockout mice fed a high-fat diet exhibited augmented and sustained RA constriction to ANG II and had elevated systemic blood pressure, when compared with normal or high-fat fed wild-type mice. Thus, Cav1, through a direct interaction, delays internalization and subsequent resensitization of AT1R. We suggest that this mechanism prevents sustained ANG II-induced RA constriction and elevated systemic blood pressure in diet-induced obesity.

Indexed as

Vascular ResistanceVasoconstrictionAngiotensin IIAnimalsArteriesCaveolaeCaveolin 2Cell MembraneHypertensionMaleMuscle, Smooth, VascularObesityProtein BindingRatsRats, WistarReceptor, Angiotensin, Type 1Angiotensin IICaveolin 2Receptor, Angiotensin, Type 1Vasoconstrictor Agentsangiotensin receptorarteriolecaveolaehypertensionobesitytrafficking

Identifiers

PMID25527780
PMCPMC4346763
OpenAlexW2100842359

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.