Evidence map›Paper›PMID 22214405›Full record

ArticleAntioxidants & redox signaling2012

NADPH oxidase-derived H(2)O(2) contributes to angiotensin II-induced aldosterone synthesis in human and rat adrenal cortical cells.

Senthilkumar B Rajamohan, Gayatri Raghuraman, Nanduri R Prabhakar, Ganesh K Kumar

Open access · greenAbstract read
In one paragraph

Article in Antioxidants & redox signaling, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

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  17. Oxidative stress in hypertension: role of the kidney.Antioxidants & redox signaling · 2014
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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

4 authors at 1 institution in 1 country.

Senthilkumar B RajamohanDepartment of Medicine, Institute for Integrative Physiology, University of Chicago, Chicago, IL 60637-1470, USA.
Gayatri Raghuraman
Nanduri R Prabhakar
Ganesh K Kumar
University of Chicago · US

Funding

Integrative Consequences of HypoxiaP01HL090554 · NHLBI · UNIVERSITY OF CHICAGO · PI PRABHAKAR, NANDURI R · 2008 to 2017
$21.4M
Neurotransmitter Metabolism in Intermittent HypoxiaR01HL089616 · NHLBI · UNIVERSITY OF CHICAGO · PI KUMAR, GANESH K · 2008 to 2011
$1.5M
NHLBI NIH HHS HL-089616NHLBI NIH HHS HL-090554
6 · The paper itself

Abstract

backgroundThe Renin-Angiotensin-Aldosterone-System plays a pivotal role in hypertension. Angiotensin II (Ang II) is a major regulator of aldosterone synthesis and secretion, and it is known to facilitate reactive oxygen species (ROS) generation in many cell types.

aimsHere, we assessed the role of ROS signaling in Ang II-induced aldosterone synthesis by focusing on the regulation of aldosterone synthase (CYP11B2), a cytochrome P450 oxidase that catalyzes the final step in aldosterone biosynthetic pathway.

resultsAng II increased CYP11B2 activity, mRNA and protein with a concomitant elevation of 6-Carboxy- 2',7'-dichlorodihydrofluorescein diacetate fluorescence, malondialdehyde and protein carbonyl levels (indices of ROS), NADPH oxidase (Nox) activity, and H(2)O(2) levels in human and rat adrenal cortical cells. The expression of nuclear receptor related 1 protein, a transcription factor known to regulate CYP11B2 expression, was also augmented by Ang II. These Ang II-evoked effects were either abolished or attenuated by pretreatment of cells with either Ang II type I receptor (AT(1)R) antagonist, or antioxidants or Nox inhibitor or siRNA silencing of Nox1, 2 and 4, or inhibitors of phospholipase C and protein kinase C. Exogenous H(2)O(2) mimicked the facilitatory effects of Ang II on CYP11B2 activity, mRNA, and protein expression, and these changes were significantly reduced by PEG-catalase. INNOVATION: ROS, particularly H(2)O(2), is identified as a key regulator of aldosterone production.

conclusionOur results suggest that Ang II facilitates CYP11B2 activity and the ensuing aldosterone production via activation of AT(1)R-Nox-H(2)O(2) signaling pathway.

Indexed as

Adrenal CortexAldosteroneAngiotensin IIAngiotensin Receptor AntagonistsAnimalsAntioxidantsCell Line, TumorCytochrome P-450 CYP11B2Enzyme InhibitorsGene ExpressionGene Expression Regulation, EnzymologicHumansHydrogen PeroxideIn Vitro TechniquesIsoenzymesMaleAldosteroneAngiotensin IIAngiotensin Receptor AntagonistsAntioxidantsCYBB protein, humanCytochrome P-450 CYP11B2Enzyme InhibitorsHydrogen PeroxideIsoenzymesMembrane GlycoproteinsNADPH Oxidase 2NADPH OxidasesNitric Oxide SynthaseNR4A2 protein, humanNuclear Receptor Subfamily 4, Group A, Member 2Receptors, AngiotensinSuperoxidesType C Phospholipases

Identifiers

PMID22214405
PMCPMC3365360
OpenAlexW1993781006

What OpenQuestion holds

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Registered trials

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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.