Evidence map›Paper›PMID 24581232›Full record

ArticleCNS neuroscience & therapeutics2014

Angiotensin converting enzyme 2/Ang-(1-7)/mas axis protects brain from ischemic injury with a tendency of age-dependence.

Jiao-Lin Zheng, Guang-Ze Li, Shu-Zhen Chen, Jin-Ju Wang, James E Olson, Hui-Jing Xia, Eric Lazartigues, Yu-Lan Zhu, Yan-Fang Chen

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Pooled it
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  10. Article
  11. Oxidative Injury in Ischemic Stroke: A Focus on NADPH Oxidase 4.Oxidative medicine and cellular longevity · 2022
    Review
  12. Article
  13. Review
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  15. Article
  16. Review
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  18. Urgent need for evaluating agonists of angiotensin-(1-7)/Mas receptor axis for treating patients with COVID-19.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2020
    Article
  19. 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

9 authors at 3 institutions in 2 countries.

Jiao-Lin ZhengDepartment of Pharmacology and Toxicology, Wright State University Boonshoft School of Medicine, Dayton, OH, USA; Department of Neurology, the Second Hospital of Harbin Medical University, Harbin, China.
Guang-Ze Li
Shu-Zhen Chen
Jin-Ju Wang
James E Olson
Hui-Jing Xia
Eric Lazartigues
Yu-Lan Zhu
Yan-Fang Chen
Wright State University · USHarbin Medical University · CNLouisiana State University Health Sciences Center New Orleans · US

Funding

Mechanisms of ACE2 Regulation in Neurogenic HypertensionR01HL093178 · NHLBI · LSU HEALTH SCIENCES CENTER · PI LAZARTIGUES, ERIC D · 2008 to 2017
$3.4M
Balance of Angiotensin II/Angiotensin (1-1): A Target in Ischemic StrokeR01HL098637 · NHLBI · WRIGHT STATE UNIVERSITY · PI CHEN, YANFANG · 2010 to 2013
$1.4M
NHLBI NIH HHS HL-093178NHLBI NIH HHS HL-098637NHLBI NIH HHS R01 HL093178
6 · The paper itself

Abstract

backgroundThe angiotensin (Ang) converting enzyme 2 (ACE2)/Ang-(1-7)/Mas receptor pathway is an important component of the renin-angiotensin system and has been suggested to exert beneficial effects in ischemic stroke.

aimsThis study explored whether the ACE2/Ang-(1-7)/Mas pathway has a protective effect on cerebral ischemic injury and whether this effect is affected by age.

methodsWe used three-month and eight-month transgenic mice with neural over-expression of ACE2 (SA) and their age-matched nontransgenic (NT) controls. Neurological deficits and ischemic stroke volume were determined following middle cerebral artery occlusion (MCAO). In oxygen and glucose deprivation (OGD) experiments on brain slices, the effects of the Mas receptor agonist (Ang1-7) or antagonist (A779) on tissue swelling, Nox2/Nox4 expression reactive oxygen species (ROS) production and cell death were measured.

results(1) Middle cerebral artery occlusion -induced ischemic injury and neurological deficit were reduced in SA mice, especially in eight-month animals; (2) OGD-induced tissue swelling and cell death were decreased in SA mice with a greater reduction seen in eight-month mice; (3) Ang-(1-7) and A779 had opposite effects on OGD-induced responses, which correlated with changes in Nox2/Nox4 expression and ROS production.

conclusionsAngiotensin converting enzyme 2/Ang-(1-7)/Mas axis protects brain from ischemic injury via the Nox/ROS signaling pathway, with a greater effect in older animals.

Indexed as

Age FactorsAngiotensin-Converting Enzyme 2Angiotensin IAngiotensin IIAnimalsBrainBrain EdemaBrain IschemiaCell DeathFemaleGlucoseHypoxia, BrainInfarction, Middle Cerebral ArteryMaleMembrane GlycoproteinsMice, Transgenic7-Ala-angiotensin (1-7)Ace2 protein, mouseAngiotensin-Converting Enzyme 2Angiotensin Iangiotensin I (1-7)Angiotensin IICybb protein, mouseGlucoseMembrane GlycoproteinsNADPH Oxidase 2NADPH Oxidase 4NADPH OxidasesNox4 protein, mousePeptide FragmentsPeptidyl-Dipeptidase AReactive Oxygen SpeciesAgingAngiotensinAngiotensin-converting enzyme 2Ischemic strokeNADPH oxidase

Identifiers

PMID24581232
PMCPMC4840841
OpenAlexW2043702192

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.