Evidence map›Paper›PMID 28465283›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2017

Expression of microRNAs and target proteins in skeletal muscle of rats selectively bred for high and low running capacity.

Samuel K Pinto, Séverine Lamon, Erin J Stephenson, Ming Kalanon, Jasmine Mikovic, Lauren G Koch, Steven L Britton, John A Hawley, Donny M Camera

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 17 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

9 authors at 5 institutions in 3 countries.

Samuel K PintoCentre for Exercise and Nutrition, Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, Victoria, Australia.
Séverine LamonSchool of Exercise and Nutrition Sciences, Institute for Physical Activity and Nutrition, Deakin University Geelong, Victoria, Australia.
Erin J StephensonDepartment of Physiology, University of Tennessee Health Science Center, Memphis, Tennessee.
Ming KalanonSchool of Exercise and Nutrition Sciences, Institute for Physical Activity and Nutrition, Deakin University Geelong, Victoria, Australia.
Jasmine MikovicSchool of Exercise and Nutrition Sciences, Institute for Physical Activity and Nutrition, Deakin University Geelong, Victoria, Australia.
Lauren G KochDepartment of Anesthesiology, University of Michigan, Ann Arbor, Michigan; and.
Steven L BrittonDepartment of Anesthesiology, University of Michigan, Ann Arbor, Michigan; and.
John A HawleyCentre for Exercise and Nutrition, Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, Victoria, Australia.
Donny M CameraCentre for Exercise and Nutrition, Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, Victoria, Australia; donny.camera@acu.edu.au.
Deakin University · AUAustralian Catholic University · AUUniversity of Michigan–Ann Arbor · USLiverpool John Moores University · GBUniversity of Tennessee Health Science Center · US

Funding

Resource for Rat Genetic Models of Aerobic CapacityP40OD021331 · OD · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI KOCH, LAUREN GERARD · 2015 to 2019
$1.9M
NIH HHS P40 OD021331
6 · The paper itself

Abstract

Impairments in mitochondrial function and substrate metabolism are implicated in the etiology of obesity and Type 2 diabetes. MicroRNAs (miRNAs) can degrade mRNA or repress protein translation and have been implicated in the development of such disorders. We used a contrasting rat model system of selectively bred high- (HCR) or low- (LCR) intrinsic running capacity with established differences in metabolic health to investigate the molecular mechanisms through which miRNAs regulate target proteins mediating mitochondrial function and substrate oxidation processes. Quantification of select miRNAs using the rat miFinder miRNA PCR array revealed differential expression of 15 skeletal muscles (musculus tibialis anterior) miRNAs between HCR and LCR rats (14 with higher expression in LCR;

Indexed as

RunningAnimalsBlotting, WesternCell LineCitrate (si)-SynthaseEnergy MetabolismExercise ToleranceIn Vitro TechniquesMiceMicroRNAsMitochondria, MuscleMuscle Fibers, SkeletalMuscle, SkeletalRatsRats, Inbred StrainsReal-Time Polymerase Chain ReactionCitrate (si)-SynthaseMicroRNAsMIRN103 microRNA, ratMIRN181 microRNA, ratMIRN194 microRNA, ratMIRN19 microRNA, ratMIRN223 microRNA, ratMIRN24 microRNA, ratMIRN26 microRNA, ratMIRN30 microRNA, ratRNA, MessengerVoltage-Dependent Anion Channel 1citrate synthasegene expressionmitochondrial dysfunctionsubstrate oxidation

Identifiers

PMID28465283
PMCPMC6189633
OpenAlexW2610655324

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.