Evidence map›Paper›PMID 30231055›Full record

ArticlePloS one2018

Oxygen conserving mitochondrial adaptations in the skeletal muscles of breath hold divers.

Thomas Kjeld, Nis Stride, Anders Gudiksen, Egon Godthaab Hansen, Henrik Christian Arendrup, Peter Frederik Horstmann, Bo Zerahn, Lars Thorbjørn Jensen, Nikolai Nordsborg, Jacob Bejder and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. 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
0.8field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

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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 1 institution in 1 country.

Thomas KjeldDepartment of Anesthesiology, Herlev Hospital, Herlev, University of Copenhagen, Denmark.ORCID 0000-0003-4348-9857
Nis StrideDepartment of Cardiology, Rigshospitalet, Copenhagen, University of Copenhagen, Denmark.
Anders GudiksenDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.
Egon Godthaab HansenDepartment of Anesthesiology, Herlev Hospital, Herlev, University of Copenhagen, Denmark.
Henrik Christian ArendrupDepartment of Cardiothoracic Surgery, Rigshospitalet, Copenhagen, University of Copenhagen, Denmark.
Peter Frederik HorstmannDepartment of Ortopedic Surgery, Hillerød Hospital, Hillerød, University of Copenhagen, Denmark.
Bo ZerahnDepartment of Clinical Physiology and Nuclear Medicine, Herlev Hospital, Herlev, University of Copenhagen, Denmark.
Lars Thorbjørn JensenDepartment of Clinical Physiology and Nuclear Medicine, Herlev Hospital, Herlev, University of Copenhagen, Denmark.
Nikolai NordsborgDepartment of Nutrition, Exercise and Sport (NEXS), Copenhagen, University of Copenhagen, Denmark.
Jacob BejderDepartment of Nutrition, Exercise and Sport (NEXS), Copenhagen, University of Copenhagen, Denmark.
Jens Frey HallingDepartment of Biology, University of Copenhagen, Copenhagen, Denmark.
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe performance of elite breath hold divers (BHD) includes static breath hold for more than 11 minutes, swimming as far as 300 m, or going below 250 m in depth, all on a single breath of air. Diving mammals are adapted to sustain oxidative metabolism in hypoxic conditions through several metabolic adaptations, including improved capacity for oxygen transport and mitochondrial oxidative phosphorylation in skeletal muscle. It was hypothesized that similar adaptations characterized human BHD. Hence, the purpose of this study was to examine the capacity for oxidative metabolism in skeletal muscle of BHD compared to matched controls.

methodsBiopsies were obtained from the lateral vastus of the femoral muscle from 8 Danish BHD and 8 non-diving controls (Judo athletes) matched for morphometry and whole body VO2max. High resolution respirometry was used to determine mitochondrial respiratory capacity and leak respiration with simultaneous measurement of mitochondrial H2O2 emission. Maximal citrate synthase (CS) and 3-hydroxyacyl CoA dehydrogenase (HAD) activity were measured in muscle tissue homogenates. Western Blotting was used to determine protein contents of respiratory complex I-V subunits and myoglobin in muscle tissue lysates.

resultsMuscle biopsies of BHD revealed lower mitochondrial leak respiration and electron transfer system (ETS) capacity and higher H2O2 emission during leak respiration than controls, with no differences in enzyme activities (CS and HAD) or protein content of mitochondrial complex subunits myoglobin, myosin heavy chain isoforms, markers of glucose metabolism and antioxidant enzymes.

conclusionWe demonstrated for the first time in humans, that the skeletal muscles of BHD are characterized by lower mitochondrial oxygen consumption both during low leak and high (ETS) respiration than matched controls. This supports previous observations of diving mammals demonstrating a lower aerobic mitochondrial capacity of the skeletal muscles as an oxygen conserving adaptation during prolonged dives.

Indexed as

Breath HoldingAdaptation, PhysiologicalAdultDivingElectron TransportHumansHydrogen PeroxideMaleMiddle AgedMitochondria, MuscleMuscle, SkeletalOxidative PhosphorylationOxygenOxygen ConsumptionSwimmingHydrogen PeroxideOxygen

Identifiers

PMID30231055
PMCPMC6145504
OpenAlexW2889917174

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.