Evidence map›Paper›PMID 28684629›Full record

ArticleCirculation research2017

Genetic Deletion of NADPH Oxidase 1 Rescues Microvascular Function in Mice With Metabolic Disease.

Jennifer A Thompson, Sebastian Larion, James D Mintz, Eric J Belin de Chantemèle, David J Fulton, David W Stepp

Open access · hybridAbstract read
In one paragraph

Article in Circulation research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

30 citing papers in PubMed, 41 citations in OpenAlex.

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  10. NADPH oxidase 1 promotes hepatic steatosis in obese mice and is abrogated by augmented skeletal muscle mass.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  11. Galectin-3 Mediates Vascular Dysfunction in Obesity by Regulating NADPH Oxidase 1.Arteriosclerosis, thrombosis, and vascular biology · 2023
    Article
  12. Article
  13. Cross-Talk of NADPH Oxidases and Inflammation in Obesity.Antioxidants (Basel, Switzerland) · 2023
    Review
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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

6 authors at 2 institutions in 2 countries.

Jennifer A ThompsonFrom the Vascular Biology Center (J.A.T., S.L., J.D.M., E.J.B.d.C., D.J.F., D.W.S.), Department of Physiology (D.W.S), Department of Pharmacology (D.J.F.), and Department of Medicine (S.L., E.J.B.d.C.), Augusta University, GA.
Sebastian LarionFrom the Vascular Biology Center (J.A.T., S.L., J.D.M., E.J.B.d.C., D.J.F., D.W.S.), Department of Physiology (D.W.S), Department of Pharmacology (D.J.F.), and Department of Medicine (S.L., E.J.B.d.C.), Augusta University, GA.
James D MintzFrom the Vascular Biology Center (J.A.T., S.L., J.D.M., E.J.B.d.C., D.J.F., D.W.S.), Department of Physiology (D.W.S), Department of Pharmacology (D.J.F.), and Department of Medicine (S.L., E.J.B.d.C.), Augusta University, GA.
Eric J Belin de ChantemèleFrom the Vascular Biology Center (J.A.T., S.L., J.D.M., E.J.B.d.C., D.J.F., D.W.S.), Department of Physiology (D.W.S), Department of Pharmacology (D.J.F.), and Department of Medicine (S.L., E.J.B.d.C.), Augusta University, GA.
David J FultonFrom the Vascular Biology Center (J.A.T., S.L., J.D.M., E.J.B.d.C., D.J.F., D.W.S.), Department of Physiology (D.W.S), Department of Pharmacology (D.J.F.), and Department of Medicine (S.L., E.J.B.d.C.), Augusta University, GA.
David W SteppFrom the Vascular Biology Center (J.A.T., S.L., J.D.M., E.J.B.d.C., D.J.F., D.W.S.), Department of Physiology (D.W.S), Department of Pharmacology (D.J.F.), and Department of Medicine (S.L., E.J.B.d.C.), Augusta University, GA. dstepp@augusta.edu.
Jisc · GBJacobson Holman (United States) · US

Funding

Novel mechanistic pathways of cardiovascular disease in obesityR01HL124773 · NHLBI · AUGUSTA UNIVERSITY · PI FULTON, DAVID J, STEPP, DAVID W · 2015 to 2018
$2.2M
Aldosterone Contribution to Leptin-mediated Hypertension in Obese FemalesR01HL130301 · NHLBI · AUGUSTA UNIVERSITY · PI BELIN DE CHANTEMELE, ERIC J · 2016 to 2020
$1.9M
Metabolic risk factors for vascular disease throughout the lifespanK99HD087527 · NICHD · AUGUSTA UNIVERSITY · PI THOMPSON, JENNIFER ANNE · 2016 to 2017
$171k
NHLBI NIH HHS R01 HL124773NHLBI NIH HHS R01 HL130301NICHD NIH HHS K99 HD087527
6 · The paper itself

Abstract

rationaleEarly vascular changes in metabolic disease that precipitate the development of cardiovascular complications are largely driven by reactive oxygen species accumulation, yet the extent to which excess reactive oxygen species derive from specific NADPH oxidase isoforms remains ill defined.

objectiveIdentify the role of Nox1 in the development of microvascular dysfunction in metabolic disease. METHODS AND

resultsFour genotypes were generated by breeding Nox1 knockout mice with

conclusionsNox1 deletion reduces oxidant load and restores microvascular health in

Indexed as

Gene DeletionAnimalsBlood GlucoseMaleMetabolic DiseasesMiceMice, Inbred C57BLMice, KnockoutMice, ObeseMicrovesselsMuscle, Smooth, VascularNADH, NADPH OxidoreductasesNADPH Oxidase 1Oxidative StressBlood GlucoseNADH, NADPH OxidoreductasesNADPH Oxidase 1NOX1 protein, mouseacetylcholineanimalsinsulin resistanceobesityprotein isoforms

Identifiers

PMID28684629
PMCPMC5729041
OpenAlexW2734060625

What OpenQuestion holds

Textmetadata
LicenceTDM
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.