Evidence map›Paper›PMID 35190865›Full record

ArticleEuropean journal of applied physiology2022

Repeated sprint exercise in hypoxia stimulates HIF-1-dependent gene expression in skeletal muscle.

Roberto Carlos Nava, Zachary McKenna, Zachary Fennel, Quint Berkemeier, Jeremy Ducharme, Flávio de Castro Magalhães, Fabiano Trigueiro Amorim, Christine Mermier

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In one paragraph

Article in European journal of applied physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
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  6. Endothelial metabolic zonation in the vascular network: a spatiotemporal blueprint for angiogenesis.American journal of physiology. Heart and circulatory physiology · 2025
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  7. Role of theGenes · 2024
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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

8 authors at 2 institutions in 2 countries.

Roberto Carlos NavaDepartment of Health, Exercise, and Sports Sciences, University of New Mexico, Albuquerque, NM, USA. roberto.nava@joslin.harvard.edu.ORCID http://orcid.org/0000-0003-4538-7539
Zachary McKennaDepartment of Health, Exercise, and Sports Sciences, University of New Mexico, Albuquerque, NM, USA.
Zachary FennelDepartment of Health, Exercise, and Sports Sciences, University of New Mexico, Albuquerque, NM, USA.
Quint BerkemeierDepartment of Health, Exercise, and Sports Sciences, University of New Mexico, Albuquerque, NM, USA.
Jeremy DucharmeDepartment of Health, Exercise, and Sports Sciences, University of New Mexico, Albuquerque, NM, USA.
Flávio de Castro MagalhãesDepartment of Health, Exercise, and Sports Sciences, University of New Mexico, Albuquerque, NM, USA.
Fabiano Trigueiro AmorimDepartment of Health, Exercise, and Sports Sciences, University of New Mexico, Albuquerque, NM, USA.
Christine MermierDepartment of Health, Exercise, and Sports Sciences, University of New Mexico, Albuquerque, NM, USA.
University of New Mexico · USNew Mexico Department of Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOur aim was to determine the effect of repeated sprint exercise in hypoxia on HIF-1 and HIF-1-regulated genes involved in glycolysis, mitochondrial turnover and oxygen transport. We also determined whether genes upregulated by exercise in hypoxia were dependent on the activation of HIF-1 in an in vitro model of exercise in hypoxia.

methodsEight endurance athletes performed bouts of repeated sprint exercise in control and hypoxic conditions. Skeletal muscle was sampled pre, post and 3 h post-exercise. HIF-1α protein and HIF1A, PDK1, GLUT4, VEGFA, BNIP3, PINK1 and PGC1A mRNA were measured. C2C12 myotubes were exposed to hypoxia and muscle contraction following treatment with a HIF-1α inhibitor to determine whether hypoxia-sensitive gene expression was dependent on HIF-1α.

resultsSprint exercise in hypoxia increased HIF-1α protein expression immediately post-exercise [fold change (FC) = 3.5 ± 2.0]. Gene expression of PDK1 (FC = 2.1 ± 1.2), BNIP3 (FC = 2.4 ± 1.4) and VEGFA (FC = 2.7 ± 1.7) increased 3 h post-exercise in hypoxia but not control. PGC1A mRNA increased 3 h post-exercise in control (FC = 5.16) and hypoxia (FC = 5.7 ± 4.1) but there was no difference between the trials. Results from the in vitro experiment showed that hypoxia plus contraction also increased PDK1, BNIP3, and VEGFA gene expression. These responses were inhibited when HIF-1 protein activity was suppressed.

conclusionRepeated sprint exercise in hypoxia upregulates some genes involved in glycolytic metabolism, mitochondrial turnover, and oxygen transport. HIF-1α is necessary for the expression of these genes in skeletal muscle cells.

Indexed as

ExerciseMuscle, SkeletalGene ExpressionHumansHypoxiaMuscle ContractionBNIP3C2C12Gene expressionLLTHPGC-1RSH

Identifiers

PMID35190865
OpenAlexW4212847195

What OpenQuestion holds

Textmetadata
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.