Evidence map›Paper›PMID 42443383›Full record

ArticleScientific reports2026

Sex differences in metabolic remodeling and skeletal muscle regeneration following cardiotoxin-induced injury.

Jong Beom Jin, Tori Soukup, Angelique Robinson, Ember Black, Addison Williams, Atul Pranay, Kenneth Humphries, Dong Yeon Kim, Yoo Kim, Edralin Lucas and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Jong Beom JinDepartment of Nutritional Sciences, Oklahoma State University, 420 Nancy Randolph Davis, Stillwater, OK, 74078, USA.
Tori SoukupDepartment of Nutritional Sciences, Oklahoma State University, 420 Nancy Randolph Davis, Stillwater, OK, 74078, USA.
Angelique RobinsonDepartment of Nutritional Sciences, Oklahoma State University, 420 Nancy Randolph Davis, Stillwater, OK, 74078, USA.
Ember BlackDepartment of Nutritional Sciences, Oklahoma State University, 420 Nancy Randolph Davis, Stillwater, OK, 74078, USA.
Addison WilliamsDepartment of Nutritional Sciences, Oklahoma State University, 420 Nancy Randolph Davis, Stillwater, OK, 74078, USA.
Atul PranayMetabolic Phenotyping Core, Aging & Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Kenneth HumphriesMetabolic Phenotyping Core, Aging & Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Dong Yeon KimDepartment of Food Science and Nutrition, Gyeongkuk National University, Andong, Gyeongsangbuk-Do, Republic of Korea.
Yoo KimDepartment of Nutritional Sciences, Oklahoma State University, 420 Nancy Randolph Davis, Stillwater, OK, 74078, USA.
Edralin LucasDepartment of Nutritional Sciences, Oklahoma State University, 420 Nancy Randolph Davis, Stillwater, OK, 74078, USA.
Shane M HammerSchool of Kinesiology, Applied Health, and Recreation, Oklahoma State University, Stillwater, OK, USA.
Jiyoung BaeDepartment of Nutritional Sciences, Oklahoma State University, 420 Nancy Randolph Davis, Stillwater, OK, 74078, USA. jiyoung.bae@okstate.edu.ORCID https://orcid.org/0000-0003-2367-7578

Funding

Viral sensor IFIH1 promotes SLE through an altered interferon programP20GM139763 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI Kenneth M Humphries · 2021 to 2026
$20.3M
American Heart Association 25AIREA1377296NIGMS NIH HHS P20 GM139763NIH HHS P20GM139763
6 · The paper itself

Abstract

Skeletal muscle regeneration is a dynamic biological process that requires metabolic remodeling, satellite cell activation, inflammatory responses, and tissue remodeling. Although biological sex is recognized as an important determinant of skeletal muscle regeneration, whether males and females utilize distinct metabolic programs during regeneration remains poorly understood. In the present study, we investigated sex-dependent differences in metabolic remodeling and regenerative responses following cardiotoxin (CTX)-induced skeletal muscle injury in mice. Targeted metabolomic analysis performed at 7 days post-injury (DPI) revealed clear sex-dependent metabolic remodeling. Principal component analysis and pathway enrichment analysis identified glycolysis/gluconeogenesis as the most significantly altered metabolic pathway following injury. Male mice exhibited higher levels of several glycolytic, tricarboxylic acid (TCA) cycle, and amino acid metabolites than female mice. In contrast, female mice showed greater expression of Pax7, Myf5, and Myod1, together with increased Pax7-positive cells, greater Cyclin D1 staining, and higher expression of Ccne1, Cdc2, and Cdk4. Local inflammatory responses also differed between sexes, with distinct temporal patterns of MCP-1, IL-6, TNF-α, and CD45 during regeneration. Histological analyses demonstrated greater lipid accumulation in female muscle at 7 DPI, whereas both sexes exhibited comparable percentages of centrally nucleated fibers and similar restoration of muscle architecture by 21 DPI. Together, these findings indicate that biological sex is associated with differences in metabolism, satellite cell-associated responses, inflammatory responses, and tissue remodeling during skeletal muscle regeneration. Although males and females ultimately achieved comparable structural recovery, the regenerative process differed substantially during the early phase after injury. These findings provide additional insight into the biological processes underlying sex-dependent skeletal muscle regeneration and establish a foundation for future studies investigating the mechanisms linking metabolism to regeneration.

Indexed as

GlycolysisMetabolomicsSex differencesSkeletal muscle regeneration

Identifiers

PMID42443383
PMCPMC13661242

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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.