Evidence map›Paper›PMID 22219516›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2012

Testing the oxidative stress hypothesis of aging in primate fibroblasts: is there a correlation between species longevity and cellular ROS production?

Anna Csiszar, Andrej Podlutsky, Natalia Podlutskaya, William E Sonntag, Steven Z Merlin, Eva E R Philipp, Kristian Doyle, Antonio Davila, Fabio A Recchia, Praveen Ballabh and 2 more

Open access · greenAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
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  7. Membrane lipids and maximum lifespan in clownfish.Fish physiology and biochemistry · 2022
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  8. A new approach method for characterizing inter-species toxicodynamic variability.Journal of toxicology and environmental health. Part A · 2021
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  9. Oxidative Stress, Diet and Prostate Cancer.The world journal of men's health · 2021
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  12. Review
  13. Aging Exacerbates Pressure-Induced Mitochondrial Oxidative Stress in Mouse Cerebral Arteries.The journals of gerontology. Series A, Biological sciences and medical sciences · 2015
    Article
  14. Article
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  19. Aging exacerbates obesity-induced cerebromicrovascular rarefaction, neurovascular uncoupling, and cognitive decline in mice.The journals of gerontology. Series A, Biological sciences and medical sciences · 2014
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 9 institutions in 3 countries.

Anna CsiszarReynolds Oklahoma Center on Aging, Department of Geriatric Medicine, University of Oklahoma Health Science Center, 975 NE 10th Street, BRC-1315A, Oklahoma City, OK 73104, USA. annacsiszar@ouhsc.edu
Andrej Podlutsky
Natalia Podlutskaya
William E Sonntag
Steven Z Merlin
Eva E R Philipp
Kristian Doyle
Antonio Davila
Fabio A Recchia
Praveen Ballabh
John T Pinto
Zoltan Ungvari
University of Oklahoma · USNew York Medical College · USColumbia University · USKiel University · DEScuola Superiore Sant'Anna · ITStanford University · USThe University of Texas Health Science Center at San Antonio · USUniversity of California, Irvine · USUniversity of Oklahoma Health Sciences Center · US

Funding

STRUCTURAL AND MOLECULAR CHANGES WITH AGEP01AG011370 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SONNTAG, WILLIAM EDMUND · 1995 to 2010
$10.7M
Role of SIRT1 in vasoprotectionR01AT006526 · NCCIH · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI UNGVARI, ZOLTAN ISTVAN · 2010 to 2014
$1.8M
VEGF receptor-1-mediated protection in dilated cardiomyopathyR01HL108213 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI RECCHIA, FABIO A · 2012 to 2015
$1.6M
Comparative Mechanisms of Exceptionally Slow AgingR01AG022873 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI AUSTAD, STEVEN N. · 2003 to 2007
$1.4M
San Antonio Comparative Biology of Aging CenterK07AG025063 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI AUSTAD, STEVEN N. · 2004 to 2008
$540k
Vasoprotection by Caloric Restriction Mimetics in AgingK08AG031085 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI CSISZAR, ANNA · 2010 to 2012
$518k
NCCIH NIH HHS AT006526NCCIH NIH HHS R01 AT006526NHLBI NIH HHS R01 HL108213NIA NIH HHS AG022873NIA NIH HHS AG025063NIA NIH HHS AG031085NIA NIH HHS P01 AG011370
6 · The paper itself

Abstract

The present study was conducted to test predictions of the oxidative stress theory of aging assessing reactive oxygen species production and oxidative stress resistance in cultured fibroblasts from 13 primate species ranging in body size from 0.25 to 120 kg and in longevity from 20 to 90 years. We assessed both basal and stress-induced reactive oxygen species production in fibroblasts from five great apes (human, chimpanzee, bonobo, gorilla, and orangutan), four Old World monkeys (baboon, rhesus and crested black macaques, and patas monkey), three New World monkeys (common marmoset, red-bellied tamarin, and woolly monkey), and one lemur (ring-tailed lemur). Measurements of cellular MitoSox fluorescence, an indicator of mitochondrial superoxide (O2(·-)) generation, showed an inverse correlation between longevity and steady state or metabolic stress-induced mitochondrial O2(·-) production, but this correlation was lost when the effects of body mass were removed, and the data were analyzed using phylogenetically independent contrasts. Fibroblasts from longer-lived primate species also exhibited superior resistance to H(2)O(2)-induced apoptotic cell death than cells from shorter-living primates. After correction for body mass and lack of phylogenetic independence, this correlation, although still discernible, fell short of significance by regression analysis. Thus, increased longevity in this sample of primates is not causally associated with low cellular reactive oxygen species generation, but further studies are warranted to test the association between increased cellular resistance to oxidative stressor and primate longevity.

Indexed as

AnimalsBiological EvolutionCell LineCellular SenescenceFibroblastsHaplorhiniHominidaeHumansLongevityMitochondriaOxidative StressOxygenPrimatesReactive Oxygen SpeciesSpecies SpecificityOxygenReactive Oxygen Species

Identifiers

PMID22219516
PMCPMC3403864
OpenAlexW2138155244

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.