Evidence map›Paper›PMID 32144492›Full record

ReviewEuropean journal of applied physiology2020

A focused review of myokines as a potential contributor to muscle hypertrophy from resistance-based exercise.

Stephen M Cornish, Eric M Bugera, Todd A Duhamel, Jason D Peeler, Judy E Anderson

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in European journal of applied physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04540367 (Blood Flow Restriction Training for The Shoulder), which is not on this map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 9% 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.

NCT04540367 nacompletednot on this map

Blood Flow Restriction Training for The Shoulder: A Case for Proximal Benefit

TypeinterventionalSponsorThe Methodist Hospital Research InstituteRan2017 to 2020Enrolled69ConditionsHealthyArmsBlood flow restriction therapy
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  11. Potential Vitamin E Signaling Mediators in Skeletal Muscle.Antioxidants (Basel, Switzerland) · 2024
    Review
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  17. What do we really know about the external urethral sphincter?Continence (Amsterdam, Netherlands) · 2024
    Review
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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

5 authors at 1 institution in 1 country.

Stephen M CornishFaculty of Kinesiology and Recreation Management, University of Manitoba, 117 Frank Kennedy Centre, Winnipeg, MB, R3T 2N2, Canada. Stephen.Cornish@umanitoba.ca.
Eric M BugeraFaculty of Kinesiology and Recreation Management, University of Manitoba, 117 Frank Kennedy Centre, Winnipeg, MB, R3T 2N2, Canada.
Todd A DuhamelFaculty of Kinesiology and Recreation Management, University of Manitoba, 117 Frank Kennedy Centre, Winnipeg, MB, R3T 2N2, Canada.
Jason D PeelerDepartment of Human Anatomy and Cell Science, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
Judy E AndersonDepartment of Biological Sciences, Faculty of Science, University of Manitoba, Winnipeg, MB, Canada.
University of Manitoba · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeResistance exercise induces muscle growth and is an important treatment for age-related losses in muscle mass and strength. Myokines are hypothesized as a signal conveying physiological information to skeletal muscle, possibly to "fine-tune" other regulatory pathways. While myokines are released from skeletal muscle following contraction, their role in increasing muscle mass and strength in response to resistance exercise or training is not established. Recent research identified both local and systemic release of myokines after an acute bout of resistance exercise. However, it is not known whether myokines with putative anabolic function are mechanistically involved in producing muscle hypertrophy after resistance exercise. Further, nitric oxide (NO), an important mediator of muscle stem cell activation, upregulates the expression of certain myokine genes in skeletal muscle.

methodIn the systemic context of complex hypertrophic signaling, this review: (1) summarizes literature on several well-recognized, representative myokines with anabolic potential; (2) explores the potential mechanistic role of myokines in skeletal muscle hypertrophy; and (3) identifies future research required to advance our understanding of myokine anabolism specifically in skeletal muscle.

resultThis review establishes a link between myokines and NO production, and emphasizes the importance of considering systemic release of potential anabolic myokines during resistance exercise as complementary to other signals that promote hypertrophy.

conclusionInvestigating adaptations to resistance exercise in aging opens a novel avenue of interdisciplinary research into myokines and NO metabolites during resistance exercise, with the longer-term goal to improve muscle health in daily living, aging, and rehabilitation.

Indexed as

ExerciseResistance TrainingCytokinesHumansHypertrophyMuscle, SkeletalCytokinesAnabolismCytokineMuscleMyokineNitric oxideSkeletal muscle hypertrophy

Identifiers

PMID32144492
OpenAlexW3010118646

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.