Evidence map›Paper›PMID 24859218›Full record

ArticleCell and tissue research2014

Testosterone is essential for skeletal muscle growth in aged mice in a heterochronic parabiosis model.

Indranil Sinha, Amiya P Sinha-Hikim, Amy J Wagers, Indrani Sinha-Hikim

Open access · greenAbstract read
In one paragraph

Article in Cell and tissue research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
3.6field-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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Review
  6. Article
  7. Review
  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
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  9. GDF11 and aging biology - controversies resolved and pending.The journal of cardiovascular aging · 2023
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  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. The ageing epigenome and its rejuvenation.Nature reviews. Molecular cell biology · 2020
    Review
  16. Review
  17. Article
  18. A young testicular microenvironment protects Leydig cells against age-related dysfunction in a mouse model of premature aging.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  19. Review
  20. Androgen-mediated regulation of skeletal muscle protein balance.Molecular and cellular endocrinology · 2017
    Review
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

4 authors at 3 institutions in 1 country.

Indranil SinhaDivision of Plastic Surgery, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA, isinha@partners.org.
Amiya P Sinha-Hikim
Amy J Wagers
Indrani Sinha-Hikim
Charles R. Drew University of Medicine and Science · USHarvard Stem Cell Institute · USHoward Hughes Medical Institute · US

Funding

Workshop for Junior Biostatisticians in Health ResearchU54MD007598 · NIMHD · CHARLES R. DREW UNIVERSITY OF MED & SCI · PI David Sane Martins · 2012 to 2026
$60.0M
TUFTS--FIELDINGP30AG031679 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI SHALENDER BHASIN · 2008 to 2026
$23.9M
Reversing age-related dysfunction of skeletal muscle stem cellsR01AG033053 · NIA · JOSLIN DIABETES CENTER · PI WAGERS, AMY JO · 2009 to 2014
$2.0M
Reversing age-related dysfunction of skeletal muscle stem cellsF32AG034703 · NIA · JOSLIN DIABETES CENTER · PI SINHA, INDRANIL · 2009 to 2010
$106k
NIA NIH HHS 1 P30 AG031679NIA NIH HHS 1 RO1 AG033053NIA NIH HHS F32 AG034703NIA NIH HHS P30 AG031679NIA NIH HHS R01 AG033053NIMHD NIH HHS U54 MD007598
6 · The paper itself

Abstract

As humans age, they lose both muscle mass and strength (sarcopenia). Testosterone, a circulating hormone, progressively declines in aging and is associated with loss of muscle mass and strength. The surgical joining of a young and old mouse (heterochronic parabiosis) activates Notch signaling and restores muscle regenerative potential in aged mice. We hypothesize that testosterone is at least one of the factors required for the improvement seen in muscles in old mice in heterochronic parabiosis with young mice. To test this hypothesis, we established the following heterochronic parabioses between young (Y; 5 months old) and old (O; 22-23 months old) C57BL6 male mice: (1) Y:O; (2) castrated Y:O (ØY:O); (3) castrated + testosterone-treated Y:O (ØY + T:O). A group of normal young mice received empty implants, and old mice were used as controls. Parabiotic pairings were maintained for 4 weeks prior to analysis. Serum testosterone levels were three-fold higher in young than in old mice. The ØY + T:O pairing demonstrated significantly elevated levels of serum testosterone and an improvement in gastrocnemius muscle weight, muscle ultrastructure, muscle fiber cross-sectional area, and Notch-1 expression in old mice. These changes were not present in aged mice in the ØY:O pairing. These data indicate that testosterone has a critical role in mediating the improved muscle mass and ultrastructure seen in an experimental model of heterochronic parabiosis.

Indexed as

ParabiosisAnimalsDisease Models, AnimalHypertrophyMaleMice, Inbred C57BLMuscle DevelopmentMuscle Fibers, SkeletalMuscle, SkeletalOrgan SizeReceptors, NotchSignal TransductionTestosteroneReceptors, NotchTestosterone

Identifiers

PMID24859218
PMCPMC4149819
OpenAlexW1974218300

What OpenQuestion holds

Textmetadata
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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.