Evidence map›Paper›PMID 21813872›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2011

Angiotensin II utilizes Janus kinase 2 in hypertension, but not in the physiological control of blood pressure, during low-salt intake.

Amy K L Banes-Berceli, Hind Al-Azawi, Daniel Proctor, Harvey Qu, Dominic Femminineo, Crystal Hill-Pyror, R Clinton Webb, Michael W Brands

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  11. Downregulation of KCNQ4 by Janus kinase 2.The Journal of membrane biology · 2013
    Article
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  13. Review
  14. 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 2 institutions in 1 country.

Amy K L Banes-BerceliDepartment of Physiology, Medical College of Georgia, Augusta, Georgia, USA. banesber@oakland.edu
Hind Al-Azawi
Daniel Proctor
Harvey Qu
Dominic Femminineo
Crystal Hill-Pyror
R Clinton Webb
Michael W Brands
Oakland University · USAugusta University · US

Funding

Vascular Rho-kinase Signaling in Angiotensin II hypertenP01HL074167 · NHLBI · MEDICAL COLLEGE OF GEORGIA (MCG) · PI BRANDS, MICHAEL W. · 2004 to 2008
$10.5M
Mechanisms for Cardiovascular Control Early in DiabetesR01HL056259 · NHLBI · MEDICAL COLLEGE OF GEORGIA (MCG) · PI BRANDS, MICHAEL W. · 2003 to 2016
$4.4M
Physiological Role of Activation of the JAK/STAT pathway in HypertensionR00HL091177 · NHLBI · OAKLAND UNIVERSITY · PI BANES-BERCELI, AMY · 2009 to 2011
$726k
CARDIOVASCULAR AND RENAL DYSFUNCTION IN EARLY DIABETESR29HL056259 · NHLBI · UNIVERSITY OF MISSISSIPPI MEDICAL CENTER · PI BRANDS, MICHAEL W · 1997 to 2000
$100k
Physiological Role of Activation of the JAK/STAT pathway in HypertensionK99HL091177 · NHLBI · AUGUSTA UNIVERSITY · PI BANES-BERCELI, AMY · 2008 to 2008
$90k
NHLBI NIH HHS HL-091177NHLBI NIH HHS HL-56259NHLBI NIH HHS HL-74167NHLBI NIH HHS P01 HL074167NHLBI NIH HHS R01 HL056259
6 · The paper itself

Abstract

Janus kinase (JAK) 2 is activated by ANG II in vitro and in vivo, and chronic blockade of JAK2 by the JAK2 inhibitor AG-490 has been shown recently to attenuate ANG II hypertension in mice. In this study, AG-490 was infused intravenously in chronically instrumented rats to determine if the blunted hypertension was linked to attenuation of the renal actions of ANG II. In male Sprague-Dawley rats, after a control period, ANG II at 10 ng·kg(-1)·min(-1) was infused intravenously with or without AG-490 at 10 ng·kg(-1)·min(-1) iv for 11 days. ANG II infusion (18 h/day) increased mean arterial pressure from 91 ± 3 to 168 ± 7 mmHg by day 11. That response was attenuated significantly in the ANG II + AG-490 group, with mean arterial pressure increasing only from 92 ± 5 to 127 ± 3 mmHg. ANG II infusion markedly decreased urinary sodium excretion, caused a rapid and sustained decrease in glomerular filtration rate to ∼60% of control, and increased renal JAK2 phosphorylation; all these responses were blocked by AG-490. However, chronic AG-490 treatment had no effect on the ability of a separate group of normal rats to maintain normal blood pressure when they were switched rapidly to a low-sodium diet, whereas blood pressure fell dramatically in losartan-treated rats on a low-sodium diet. These data suggest that activation of the JAK/STAT pathway is critical for the development of ANG II-induced hypertension by mediating its effects on renal sodium excretory capability, but the physiological control of blood pressure by ANG II with a low-salt diet does not require JAK2 activation.

Indexed as

Diet, Sodium-RestrictedAngiotensin IIAnimalsBlood PressureDisease Models, AnimalEnzyme InhibitorsGlomerular Filtration RateHypertensionInfusions, IntravenousJanus Kinase 2MalePhosphorylationRatsRats, Sprague-DawleySignal TransductionSTAT3 Transcription Factoralpha-cyano-(3,4-dihydroxy)-N-benzylcinnamideAngiotensin IIEnzyme InhibitorsJak2 protein, ratJanus Kinase 2Stat3 protein, ratSTAT3 Transcription FactorTyrphostins

Identifiers

PMID21813872
PMCPMC3197339
OpenAlexW1975926008

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.