Evidence map›Paper›PMID 26273023›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2016

Increased Adipocyte Area in Injured Muscle With Aging and Impaired Remodeling in Female Mice.

Caitlin M Fearing, David W Melton, Xiufen Lei, Heather Hancock, Hanzhou Wang, Zaheer U Sarwar, Laurel Porter, Matthew McHale, Linda M McManus, Paula K Shireman

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Skeletal Muscle Regeneration in Cardiotoxin-Induced Muscle Injury Models.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. 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

10 authors.

Caitlin M FearingDepartment of Surgery.
David W MeltonDepartment of Surgery, Department of Cellular and Structural Biology, Sam and Ann Barshop Institute for Longevity and Aging Studies.
Xiufen LeiDepartment of Surgery.
Heather HancockDepartment of Surgery.
Hanzhou WangDepartment of Surgery.
Zaheer U SarwarDepartment of Surgery.
Laurel PorterDepartment of Surgery.
Matthew McHaleDepartment of Surgery.
Linda M McManusSam and Ann Barshop Institute for Longevity and Aging Studies, Department of Pathology, and Department of Periodontics, University of Texas Health Science Center, San Antonio.
Paula K ShiremanDepartment of Surgery, Sam and Ann Barshop Institute for Longevity and Aging Studies, The South Texas Veterans Health Care System, San Antonio. shireman@uthscsa.edu.

Funding

Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
CHEMOKINES AND IMMUNE CELLS IN HIND LIMB ISCHEMIAR01HL074236 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SHIREMAN, PAULA K · 2003 to 2011
$3.0M
Improved Muscle Regeneration by Anti-miRNA Alteration in Macrophage PolarizationF30HL110743 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI MELTON, DAVID · 2011 to 2015
$158k
BLRD VA I01 BX001186NCATS NIH HHS UL1 TR001120NHLBI NIH HHS F30 HL110743NHLBI NIH HHS R01 HL074236
6 · The paper itself

Abstract

We demonstrated that young male and female mice similarly regenerated injured skeletal muscle; however, female mice transiently increased adipocyte area within regenerated muscle in a sex hormone-dependent manner. We extended these observations to investigate the effect of aging and sex on sarcopenia and muscle regeneration. Cardiotoxin injury to the tibialis anterior muscle of young, middle, and old-aged C57Bl/6J male and female mice was used to measure regenerated myofiber cross-sectional area (CSA), adipocyte area, residual necrosis, and inflammatory cell recruitment. Baseline (uninjured) myofiber CSA was decreased in old mice of both sexes compared to young and middle-aged mice. Regenerated CSA was similar in male mice in all age groups until baseline CSA was attained but decreased in middle and old age female mice compared to young females. Furthermore, adipocyte area within regenerated muscle was transiently increased in young females compared to young males and these sex-dependent increases persisted in middle and old age female mice and were associated with increased Pparg Young female mice had more pro-inflammatory monocytes/macrophages in regenerating muscle than young male mice and increased Sca-1(+)CD45(-)cells. In conclusion, sex and age influence pro-inflammatory cell recruitment, muscle regeneration, and adipocyte area following skeletal muscle injury.

Indexed as

AgingRegenerationAdipocytesAnimalsCardiotoxinsDisease Models, AnimalFemaleMacrophagesMaleMiceMice, Inbred C57BLMonocytesMuscle, SkeletalSarcopeniaSex CharacteristicsCardiotoxinsMonocyte/macrophageMuscle regenerationSarcopenia

Identifiers

PMID26273023
PMCPMC4945881

What OpenQuestion holds

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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.