Evidence map›Paper›PMID 28698572›Full record

ArticleScientific reports2017

The effect of calorie restriction on mouse skeletal muscle is sex, strain and time-dependent.

Luisa Boldrin, Jacob A Ross, Charlotte Whitmore, Bruno Doreste, Charlotte Beaver, Ayad Eddaoudi, Daniel J Pearce, Jennifer E Morgan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

37 citing papers in PubMed, 51 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

8 authors at 4 institutions in 2 countries.

Luisa BoldrinDubowitz Neuromuscular Centre, Molecular Neurosciences Section, Developmental Neurosciences Programme, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N1EH, UK.
Jacob A RossDubowitz Neuromuscular Centre, Molecular Neurosciences Section, Developmental Neurosciences Programme, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N1EH, UK.
Charlotte WhitmoreDubowitz Neuromuscular Centre, Molecular Neurosciences Section, Developmental Neurosciences Programme, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N1EH, UK.
Bruno DoresteDubowitz Neuromuscular Centre, Molecular Neurosciences Section, Developmental Neurosciences Programme, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N1EH, UK.
Charlotte BeaverUCL Institute of Healthy Ageing, University College London, London, WC1E 6BT, UK.
Ayad EddaoudiFlow Cytometry Core Facility, UCL Great Ormond Street Institute of Child Health, Camelia Botnar Laboratories, Great Ormond Street Hospital, 85 Lamb's Conduit, London, WC1N 3JH, UK.ORCID 0000-0001-5272-6426
Daniel J PearceUCL Institute of Healthy Ageing, University College London, London, WC1E 6BT, UK.
Jennifer E MorganDubowitz Neuromuscular Centre, Molecular Neurosciences Section, Developmental Neurosciences Programme, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London, WC1N1EH, UK. jennifer.morgan@ucl.ac.uk.
University College London · GBMRC Unit for Lifelong Health and Ageing · GBGreat Ormond Street Hospital · GBInstitute of Child Health · GR

Funding

Biotechnology and Biological Sciences Research Council BB/J005436/1
6 · The paper itself

Abstract

Loss of skeletal muscle mass and function occurs with increasing age. Calorie restriction (CR) increases the lifespan of C57Bl/6 mice, but not in the shorter-lived DBA/2 strain. There is some evidence that calorie restriction reduces or delays many of the age-related defects that occur in rodent skeletal muscle. We therefore investigated the effect of short (2.5 month) and longer term (8.5 and 18.5 months) CR on skeletal muscle in male and female C57Bl/6 and DBA/2 mice. We found that short-term CR increased the satellite cell number and collagen VI content of muscle, but resulted in a delayed regenerative response to injury.Consistent with this, the in vitro proliferation of satellite cells derived from these muscles was reduced by CR. The percentage of stromal cells, macrophages, hematopoietic stem cells and fibroadipogenic cells in the mononucleated cell population derived from skeletal muscle was reduced by CR at various stages. But overall, these changes are neither consistent over time, nor between strain and sex. The fact that changes induced by CR do not persist with time and the dissimilarities between the two mouse strains, combined with sex differences, urge caution in applying CR to improve skeletal muscle function across the lifespan in humans.

Indexed as

AnimalsBody WeightCaloric RestrictionCell ProliferationCells, CulturedCollagen Type VIEnergy MetabolismFemaleMaleMiceMice, Inbred C57BLMice, Inbred DBAMuscle, SkeletalSatellite Cells, Skeletal MuscleSex CharacteristicsTime FactorsCollagen Type VI

Identifiers

PMID28698572
PMCPMC5505993
OpenAlexW2730599742

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.