Evidence mapPaperPMID 40448802Full record

ArticleThe Journal of physiology2025

Mitochondrial haplotype and sex modulate responses to endurance exercise training.

Bumsoo Ahn, Tianhao Wei, Ryan Pettit-Mee, Eunyoung Kim, Robert V Musci, Jonathan Wanagat, Hoang Van M Nguyen, Arlan Richardson, Hyunyoung Kim

Abstract read
In one paragraph

Article in The Journal of physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Bumsoo AhnDepartment of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.ORCID https://orcid.org/0000-0002-2743-7099
Tianhao WeiDepartment of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.ORCID https://orcid.org/0009-0000-6003-0592
Ryan Pettit-MeeDepartment of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Eunyoung KimDepartment of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Robert V MusciDepartment of Health and Human Sciences, Frank R Seaver College of Science and Engineering, Loyola Marymount University, Los Angeles, California, USA.ORCID https://orcid.org/0000-0001-9123-3472
Jonathan WanagatDivisions of Geriatrics, Department of Medicine, University of California Los Angeles, Los Angeles, California, USA.ORCID https://orcid.org/0000-0002-8460-8616
Hoang Van M NguyenDepartment of Nutritional Sciences, University of Oklahoma Health Sciences, Oklahoma City, Oklahoma, USA.
Arlan RichardsonOklahoma City VA Medical Center, Oklahoma City, Oklahoma, USA.
Hyunyoung KimDepartment of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.

Funding

A New Translational Rat Model for Evaluating Anti-Aging InterventionsR33AG072137 · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · 2025 to 2025
$714k
Mitochondrial DNA Deletion Mutation Frequency as a Metric of Biologic AgeR01AG069924 · UNIVERSITY OF CALIFORNIA LOS ANGELES · 2025 to 2025
$409k
Mitochondrial biogenesis, genetics and cell loss in mammalian agingR01AG055518 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JUDD M. AIKEN, Allen Herbst · 2021 to 2021
$401k
Relationship of exercise frequency, intensity, and fitness to improved cognition and biomarkers in Gerofit participantsI01RX004521 · VA GREATER LOS ANGELES HEALTHCARE SYSTEM · 2025 to 2025
BLRD VA IK6 BX005238HHS | NIH | National Institute on Aging (NIA) AG072137HHS | NIH | National Institute on Aging (NIA) I01RX004521HHS | NIH | National Institute on Aging (NIA) K02AG059847HHS | NIH | National Institute on Aging (NIA) R00AG064143HHS | NIH | National Institute on Aging (NIA) R01AG055518HHS | NIH | National Institute on Aging (NIA) R01AG069924NIA NIH HHS K02 AG059847NIA NIH HHS R00 AG064143NIA NIH HHS R01 AG055518NIA NIH HHS R01 AG069924NIA NIH HHS R01 AG092766NIA NIH HHS R33 AG072137RRD VA I01 RX004521U.S. Department of Veterans Affairs (VA) 1IK6BX005238
6 · The paper itself

Abstract

Heterogeneity in the response to exercise training is widely demonstrated in the literature. Although the variability in exercise acclimation is not entirely understood, a large portion of exercise response variability is attributable to genetic heritability potentially due to inherited maternal mitochondrial characteristics. Humans exhibit a heterogenous genome and mitochondrial haplotype; however much of the preclinical research proposed to investigate molecular transducers of exercise has been implemented using mouse models that lack mitochondrial and nuclear genomic diversity. Leveraging a novel rat model of heterogeneous genome, OKC-HET rats, we investigated the impact of mitochondrial (mt) haplotype on exercise training. We hypothesized that rats with divergent mitochondrial genomes will respond differently to endurance exercise training. OKC-HET rats aged 18-19 months old were subjected to 8 weeks of voluntary wheel running as their endurance exercise training programme. We found mt haplotype-specific effects on responses to endurance exercise and motor co-ordination, which were consistent with mitochondrial bioenergetics and markers of oxidative stress. Mitochondrial copy number and the expression of mitochondrial proteins were similar between the two mt haplotypes, suggesting intrinsic alterations of mitochondrial functions by the two distinct mitochondrial genomes. Motor co-ordination and fragmentation of acetylcholine receptors were also affected by mitochondrial haplotype. The mt haplotype effects on training responses were specific to biological sex also. Collectively we report that mitochondrial haplotype significantly affects responses to endurance exercise in a sex-specific manner. KEY POINTS: Mitochondrial haplotype affects the responses to endurance exercise. Sex modulates the effects of mitochondrial haplotype in the responses to endurance training. Mitochondrial DNA (mtDNA) deletion frequency increases following endurance exercise. mtDNA deletion frequency is higher in males than females after endurance exercise in OKC-HET rats.

Indexed as

endurance exercisemitochondrial bioenergeticsmitochondrial DNAmitochondrial haplotypemotor co‐ordinationneuromuscular junctionsex

Identifiers

PMID40448802
PMCPMC13127427

What Socratic holds

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Registered trials

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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 Socratic graph.