Evidence map›Paper›PMID 41326383›Full record

Trial reportNature communications2025

Sprint interval exercise disrupts mitochondrial ultrastructure driving a unique mitochondrial stress response and remodelling in men.

J Botella, E Perri, N J Caruana, S López-Calcerrada, M Brischigliaro, N A Jamnick, V Oorschot, N J Saner, J Díaz-Lara, D F Taylor and 7 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. 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

17 authors.

J BotellaInstitute for Health and Sport (IHES), Victoria University, Melbourne, Australia. javier.botella.ruiz@gmail.com.ORCID http://orcid.org/0000-0001-9722-8519
E PerriInstitute for Health and Sport (IHES), Victoria University, Melbourne, Australia.
N J CaruanaInstitute for Health and Sport (IHES), Victoria University, Melbourne, Australia.ORCID http://orcid.org/0000-0002-0817-1686
S López-CalcerradaHospital 12 de Octubre Research Institute (i+12), Madrid, Spain.ORCID http://orcid.org/0000-0002-0385-8067
M BrischigliaroVeneto Institute of Molecular Medicine, Padova, Italy.ORCID http://orcid.org/0000-0003-1520-1342
N A JamnickInstitute for Health and Sport (IHES), Victoria University, Melbourne, Australia.
V OorschotMonash Ramaciotti Centre for Cryo Electron Microscopy, Monash University, Melbourne, Australia.ORCID http://orcid.org/0000-0002-8122-8271
N J SanerInstitute for Health and Sport (IHES), Victoria University, Melbourne, Australia.
J Díaz-LaraInstitute for Health and Sport (IHES), Victoria University, Melbourne, Australia.ORCID http://orcid.org/0000-0003-1970-6313
D F TaylorInstitute for Health and Sport (IHES), Victoria University, Melbourne, Australia.
A GarnhamInstitute for Health and Sport (IHES), Victoria University, Melbourne, Australia.
E Fernández-VizarraVeneto Institute of Molecular Medicine, Padova, Italy.ORCID http://orcid.org/0000-0002-2469-142X
C UgaldeHospital 12 de Octubre Research Institute (i+12), Madrid, Spain.
G RammMonash Ramaciotti Centre for Cryo Electron Microscopy, Monash University, Melbourne, Australia.ORCID http://orcid.org/0000-0003-3596-2288
D A StroudDepartment of Biochemistry and Pharmacology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Australia.ORCID http://orcid.org/0000-0002-2048-3383
M LazarouDepartment of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Melbourne, Australia.ORCID http://orcid.org/0000-0003-2150-5545
D J BishopInstitute for Health and Sport (IHES), Victoria University, Melbourne, Australia. david.bishop@vu.edu.au.ORCID http://orcid.org/0000-0002-6956-9188

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exercise is a key lifestyle intervention for mitochondrial health, yet the molecular mechanisms by which different exercise prescriptions regulate mitochondrial remodeling remain unclear. We conducted an open-label counterbalanced randomized controlled trial (ACTRN12617001105336) and observed that sprint-interval exercise (SIE; n = 14), compared to moderate-intensity continuous exercise (MICE; n = 14), induces a mitochondrial stress signature and unfolded protein response (UPR

Indexed as

ExerciseHigh-Intensity Interval TrainingMitochondriaAdultAnimalsCitric Acid CycleHumansMaleMiceOxidative PhosphorylationStress, PhysiologicalUnfolded Protein ResponseYoung Adult

Identifiers

PMID41326383
PMCPMC12769668

What Socratic 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 Socratic graph.