Evidence map›Paper›PMID 32192914›Full record

ArticleEBioMedicine2020

Social stress is lethal in the mdx model of Duchenne muscular dystrophy.

Maria Razzoli, Angus Lindsay, Michelle L Law, Christopher M Chamberlain, William M Southern, Madeleine Berg, John Osborn, William C Engeland, Joseph M Metzger, James M Ervasti and 1 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Synthetic bottlebrush block copolymer prevents disease onset in Duchenne muscular dystrophy.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
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  7. Review
  8. Article
  9. Review
  10. The behavioural consequences of dystrophinopathy.Disease models & mechanisms · 2025
    Article
  11. Article
  12. Article
  13. Animal Models Relevant for Geroscience: Current Trends and Future Perspectives in Biomarkers, and Measures of Biological Aging.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
    Review
  14. Article
  15. Article
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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

11 authors at 2 institutions in 1 country.

Maria RazzoliDepartment of Integrative Biology and Physiology, University of Minnesota Medical School, Minneapolis, MN, United States.
Angus LindsayDepartment of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota Medical School, Minneapolis, MN, United States.
Michelle L LawDepartment of Integrative Biology and Physiology, University of Minnesota Medical School, Minneapolis, MN, United States.
Christopher M ChamberlainDepartment of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota Medical School, Minneapolis, MN, United States.
William M SouthernDepartment of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota Medical School, Minneapolis, MN, United States.
Madeleine BergDepartment of Integrative Biology and Physiology, University of Minnesota Medical School, Minneapolis, MN, United States.
John OsbornDepartment of Integrative Biology and Physiology, University of Minnesota Medical School, Minneapolis, MN, United States.
William C EngelandDepartment of Neuroscience, University of Minnesota Medical School, Minneapolis, MN, United States.
Joseph M MetzgerDepartment of Integrative Biology and Physiology, University of Minnesota Medical School, Minneapolis, MN, United States.
James M ErvastiDepartment of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota Medical School, Minneapolis, MN, United States. Electronic address: jervasti@umn.edu.
Alessandro BartolomucciDepartment of Integrative Biology and Physiology, University of Minnesota Medical School, Minneapolis, MN, United States. Electronic address: abartolo@umn.edu.
University of Minnesota Medical Center · USUniversity of Minnesota · US

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Jeffrey S. Miller · 1998 to 2026
$100.4M
TRAINING PROGRAM IN MUSCLE RESEARCHT32AR007612 · NIAMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI JAMES M ERVASTI, DAWN A LOWE · 2001 to 2026
$11.3M
CYTOSKELETAL INTERACTIONS OF DYSTROPHINR01AR042423 · NIAMS · UNIVERSITY OF WISCONSIN MADISON · PI ERVASTI, JAMES M · 1994 to 2025
$9.3M
Costamere Defects in Muscular DystrophiesR01AR049899 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI ERVASTI, JAMES M · 2005 to 2025
$8.2M
NCI NIH HHS P30 CA077598NIAMS NIH HHS R01 AR042423NIAMS NIH HHS R01 AR049899NIAMS NIH HHS T32 AR007612
6 · The paper itself

Abstract

backgroundDuchenne muscular dystrophy (DMD) is caused by the loss of dystrophin. Severe and ultimately lethal, DMD progresses relatively slowly in that patients become wheelchair bound only around age twelve with a survival expectancy reaching the third decade of life.

methodsThe mildly-affected mdx mouse model of DMD, and transgenic DysΔMTB-mdx and Fiona-mdx mice expressing dystrophin or utrophin, respectively, were exposed to either mild (scruffing) or severe (subordination stress) stress paradigms and profiled for their behavioral and physiological responses. A subgroup of mdx mice exposed to subordination stress were pretreated with the beta-blocker metoprolol.

findingsSubordination stress caused lethality in ∼30% of mdx mice within 24 h and ∼70% lethality within 48 h, which was not rescued by metoprolol. Lethality was associated with heart damage, waddling gait and hypo-locomotion, as well as marked up-regulation of the hypothalamus-pituitary-adrenocortical axis. A novel cardiovascular phenotype emerged in mdx mice, in that scruffing caused a transient drop in arterial pressure, while subordination stress caused severe and sustained hypotension with concurrent tachycardia. Transgenic expression of dystrophin or utrophin in skeletal muscle protected mdx mice from scruffing and social stress-induced responses including mortality.

interpretationWe have identified a robust new stress phenotype in the otherwise mildly affected mdx mouse that suggests relatively benign handling may impact the outcome of behavioural experiments, but which should also expedite the knowledge-based therapy development for DMD.

fundingGreg Marzolf Jr. Foundation, Summer's Wish Fund, NIAMS, Muscular Dystrophy Association, University of Minnesota and John and Cheri Gunvalson Trust.

Indexed as

Adrenergic beta-AntagonistsAnimalsArterial PressureDisease Models, AnimalDystrophinGait Disorders, NeurologicGene ExpressionHeart FailureHumansHypotensionHypothalamo-Hypophyseal SystemMaleMetoprololMiceMice, Inbred mdxMuscle, SkeletalAdrenergic beta-AntagonistsDystrophinMetoprololUtrophinHPA-axisHypertensionMuscular dystrophySocial stressUtrophin

Identifiers

PMID32192914
PMCPMC7251247
OpenAlexW3011885018

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.