Evidence map›Paper›PMID 37115626›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2023

Female C57BL/6N mice are a viable model of aortic aging in women.

Abigail G Longtine, Ravinandan Venkatasubramanian, Melanie C Zigler, Alexandra J Lindquist, Sophia A Mahoney, Nathan T Greenberg, Nicholas S VanDongen, Katelyn R Ludwig, Kerrie L Moreau, Douglas R Seals and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.6field-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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. The impact of age and sex on cerebral and large artery stiffness and the response to pulse pressure.American journal of physiology. Heart and circulatory physiology · 2025
    Article
  6. Review
  7. X's, Y's, and vascular ties: exploring the role of sex chromosomes in arterial stiffness and vascular aging.American journal of physiology. Heart and circulatory physiology · 2025
    Article
  8. Role of the circulating milieu in age-related arterial dysfunction: a novel ex vivo approach.American journal of physiology. Heart and circulatory physiology · 2024
    Article
  9. Review
  10. Review
  11. 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

11 authors at 2 institutions in 1 country.

Abigail G LongtineDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.ORCID 0000-0001-7905-8341
Ravinandan VenkatasubramanianDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.
Melanie C ZiglerDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.ORCID 0000-0002-2058-4897
Alexandra J LindquistDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.
Sophia A MahoneyDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.ORCID 0000-0002-0013-4514
Nathan T GreenbergDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.ORCID 0000-0001-5174-3195
Nicholas S VanDongenDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.
Katelyn R LudwigDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.ORCID 0009-0005-0592-2711
Kerrie L MoreauUniversity of Colorado Anschutz Medical Campus, Aurora, Colorado, United States.ORCID 0000-0001-9298-047X
Douglas R SealsDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.ORCID 0000-0002-2391-9824
Zachary S ClaytonDepartment of Integrative Physiology, University of Colorado Boulder, Boulder, Colorado, United States.ORCID 0000-0003-3878-3533
University of Colorado Boulder · USUniversity of Colorado Anschutz Medical Campus · US

Funding

University of Colorado Aging Training GrantT32AG000279 · NIA · UNIVERSITY OF COLORADO DENVER · PI Kerrie Moreau · 2001 to 2026
$10.1M
Translational studies of cellular senescence as a regulator of doxorubicin-mediated arterial dysfunctionK99HL159241 · NHLBI · UNIVERSITY OF COLORADO · PI CLAYTON, ZACHARY S. · 2022 to 2023
$350k
Targeting cellular senescence with oral fisetin supplementation to improve vascular agingF31HL165885 · NHLBI · UNIVERSITY OF COLORADO · PI MAHONEY, SOPHIA ANDREA · 2022 to 2025
$123k
Mitochondrial oxidative stress: a target for treatment of doxorubicin-associated vascular endothelial dysfunctionF32HL151022 · NHLBI · UNIVERSITY OF COLORADO · PI CLAYTON, ZACHARY S. · 2020 to 2021
$89k
Role of the human gut microbiome and related metabolites for causally mediating vascular endothelial functionF31HL160173 · NHLBI · UNIVERSITY OF COLORADO · PI LONGTINE, ABIGAIL GRACE · 2022 to 2023
$65k
NHLBI NIH HHS F31 HL160173NHLBI NIH HHS F31 HL165885NHLBI NIH HHS F32 HL151022NHLBI NIH HHS K99 HL159241NIA NIH HHS T32 AG000279
6 · The paper itself

Abstract

The aorta stiffens with aging in both men and women, which predicts cardiovascular mortality. Aortic wall structural and extracellular matrix (ECM) remodeling, induced in part by chronic low-grade inflammation, contribute to aortic stiffening. Male mice are an established model of aortic aging. However, there is little information regarding whether female mice are an appropriate model of aortic aging in women, which we aimed to elucidate in the present study. We assessed two strains of mice and found that in C57BL/6N mice, in vivo aortic stiffness (pulse wave velocity, PWV) was higher with aging in both sexes, whereas in B6D2F1 mice, PWV was higher in old versus young male mice, but not in old versus young female mice. Because the age-related stiffening that occurs in men and women was reflected in male and female C57BL/6N mice, we examined the mechanisms of stiffening in this strain. In both sexes, aortic modulus of elasticity (pin myography) was lower in old mice, occurred in conjunction with and was related to higher plasma levels of the elastin-degrading enzyme matrix metalloproteinase-9 (MMP-9), and was accompanied by higher numbers of aortic elastin breaks and higher abundance of adventitial collagen-1. Plasma levels of the inflammatory cytokines interferon-γ, interleukin 6, and monocyte chemoattractant protein-1 were higher in both sexes of old mice. In conclusion, female C57BL/6N mice exhibit aortic stiffening, reduced modulus of elasticity and structural/ECM remodeling, and associated increases in MMP-9 and systemic inflammation with aging, and thus are an appropriate model of aortic aging in women.

Indexed as

ElastinVascular StiffnessAgingAnimalsAortaFemaleHumansInflammationMaleMatrix Metalloproteinase 9MiceMice, Inbred C57BLPulse Wave AnalysisElastinMatrix Metalloproteinase 9aginganimal modelsartery stiffeningpulse wave velocitysex differences

Identifiers

PMID37115626
PMCPMC10202480
OpenAlexW4367310873

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.