Evidence map›Paper›PMID 36835034›Full record

ArticleInternational journal of molecular sciences2023

Glucose 6-P Dehydrogenase Overexpression Improves Aging-Induced Endothelial Dysfunction in Aorta from Mice: Role of Arginase II.

Eva Serna, Maria D Mauricio, Teresa San-Miguel, Sol Guerra-Ojeda, David Verdú, Alicia Valls, Coralie Arc-Chagnaud, Adrián De la Rosa, José Viña

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 1 institution in 1 country.

Eva SernaDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0002-2968-3349
Maria D MauricioDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0002-7695-2898
Teresa San-MiguelDepartment of Pathology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.
Sol Guerra-OjedaDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.
David VerdúDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.
Alicia VallsDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0001-5653-9409
Coralie Arc-ChagnaudDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0001-6655-8734
Adrián De la RosaDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0001-6854-5988
José ViñaDepartment of Physiology, Faculty of Medicine, University of Valencia, 46010 Valencia, Spain.ORCID 0000-0001-9709-0089
Universitat de València · ES

Funding

Conselleria de Sanitat de la Generalitat Valenciana PROMETEO/2019/097Instituto de Salud Carlos III CB16/10/00435 (CIBERFES)Spanish Ministry of Innovation and Science PID2019-110906RB-I00/AEI/10.13039/501100011033
6 · The paper itself

Abstract

The increase of vascular arginase activity during aging causes endothelial dysfunction. This enzyme competes with the endothelial nitric oxide synthase (eNOS) for L-arginine substrate. Our hypothesis is that glucose 6-P dehydrogenase (G6PD) overexpression could improve the endothelial function modulating the arginase pathway in aorta from mice. For this study, three groups of male mice were used: young wild type (WT) (6-9 months), old WT (21-22 months) and old G6PD-Tg (21-22 months) mice. Vascular reactivity results showed a reduced acetylcholine-dependent relaxation in the old WT but not old G6PD-Tg group. Endothelial dysfunction was reverted by nor-NOHA, an arginase inhibitor. Mice overexpressing G6PD underexpressed arginase II and also displayed a lower activity of this enzyme. Moreover, histological analyses demonstrated that age causes a thickness of aortic walls, but this did not occur in G6PD-Tg mice. We conclude that the overexpressing G6PD mouse is a model to improve vascular health via the arginase pathway.

Indexed as

ArginaseGlucosephosphate DehydrogenaseVascular DiseasesAgingAnimalsAortaArginineEndothelium, VascularGlucoseMaleMiceNitric OxideNitric Oxide Synthase Type IIIArg2 protein, mouseArginaseArginineGlucoseGlucosephosphate DehydrogenaseNitric OxideNitric Oxide Synthase Type IIIagingaortaarginaseG6PDnitric oxidevascular reactivity

Identifiers

PMID36835034
PMCPMC9961129
OpenAlexW4320495900

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.