Evidence map›Paper›PMID 23997094›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2013

Transcriptional and phenotypic changes in aorta and aortic valve with aging and MnSOD deficiency in mice.

Carolyn M Roos, Michael Hagler, Bin Zhang, Elise A Oehler, Arman Arghami, Jordan D Miller

Open access · greenAbstract readComparative Study
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
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  5. Physical Resilience as a Predictor of Lifespan and Late-Life Health in Genetically Heterogeneous Mice.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
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  13. Screening Analysis of Sirtuins Family Expression on Anti-Inflammation of Resveratrol in Endothelial Cells.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
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  15. Article
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  19. Cellular senescence: Implications for metabolic disease.Molecular and cellular endocrinology · 2017
    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 1 institution in 1 country.

Carolyn M RoosDepartment of Surgery, Mayo Clinic, Rochester, Minnesota;
Michael Hagler
Bin Zhang
Elise A Oehler
Arman Arghami
Jordan D Miller
Mayo Clinic · US

Funding

Role of SIRT6 in calcific aortic valve diseaseR01HL111121 · NHLBI · MAYO CLINIC ROCHESTER · PI MILLER, JORDAN D · 2013 to 2017
$2.0M
Oxidative stress and aortic valve diseaseR00HL092235 · NHLBI · MAYO CLINIC ROCHESTER · PI MILLER, JORDAN D · 2009 to 2011
$747k
Oxidative stress and aortic valve diseaseK99HL092235 · NHLBI · UNIVERSITY OF IOWA · PI MILLER, JORDAN D · 2008 to 2008
$107k
NHLBI NIH HHS HL-092235NHLBI NIH HHS HL-111121NHLBI NIH HHS R01 HL111121
6 · The paper itself

Abstract

The purpose of this study was to characterize changes in antioxidant and age-related gene expression in aorta and aortic valve with aging, and test the hypothesis that increased mitochondrial oxidative stress accelerates age-related endothelial and aortic valve dysfunction. Wild-type (MnSOD(+/+)) and manganese SOD heterozygous haploinsufficient (MnSOD(+/-)) mice were studied at 3 and 18 mo of age. In aorta from wild-type mice, antioxidant expression was preserved, although there were age-associated increases in Nox2 expression. Haploinsufficiency of MnSOD did not alter antioxidant expression in aorta, but increased expression of Nox2. When compared with that of aorta, age-associated reductions in antioxidant expression were larger in aortic valves from wild-type and MnSOD haploinsufficient mice, although Nox2 expression was unchanged. Similarly, sirtuin expression was relatively well-preserved in aorta from both genotypes, whereas expression of SIRT1, SIRT2, SIRT3, SIRT4, and SIRT6 were significantly reduced in the aortic valve. Expression of p16(ink4a), a marker of cellular senescence, was profoundly increased in both aorta and aortic valve from MnSOD(+/+) and MnSOD(+/-) mice. Functionally, we observed comparable age-associated reductions in endothelial function in aorta from both MnSOD(+/+) and MnSOD(+/-) mice. Interestingly, inhibition of NAD(P)H oxidase with apocynin or gp91ds-tat improved endothelial function in MnSOD(+/+) mice but significantly impaired endothelial function in MnSOD(+/-) mice at both ages. Aortic valve function was not impaired by aging or MnSOD haploinsufficiency. Changes in antioxidant and sirtuin gene expression with aging differ dramatically between aorta and aortic valve. Furthermore, although MnSOD does not result in overt cardiovascular dysfunction with aging, compensatory transcriptional responses to MnSOD deficiency appear to be tissue specific.

Indexed as

Oxidative StressTranscription, GeneticAge FactorsAgingAnimalsAntioxidantsAorta, ThoracicAortic ValveCalciumCellular SenescenceCyclin-Dependent Kinase Inhibitor p16Dose-Response Relationship, DrugEnzyme InhibitorsForkhead Transcription FactorsGene Expression RegulationGenotypeAntioxidantsCalciumCyclin-Dependent Kinase Inhibitor p16Enzyme InhibitorsForkhead Transcription FactorsInflammation MediatorsNADPH OxidasesNitric Oxide SynthaseSirtuinsSuperoxide DismutaseSuperoxide Dismutase 2Vasodilator Agentsagingaortaaortic valveendothelial functionmitochondrial oxidative stress

Identifiers

PMID23997094
PMCPMC3840262
OpenAlexW1966990212

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.