Evidence map›Paper›PMID 26290460›Full record

ArticleAging cell2015

The histone deacetylase inhibitor butyrate improves metabolism and reduces muscle atrophy during aging.

Michael E Walsh, Arunabh Bhattacharya, Kavithalakshmi Sataranatarajan, Rizwan Qaisar, Lauren Sloane, Md M Rahman, Michael Kinter, Holly Van Remmen

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 203 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
203citing papers in PubMed, 8 pooled it
6.8field-weighted citation impact, top 2% 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

203 citing papers in PubMed, 8 syntheses or guidelines pooled it, 314 citations in OpenAlex.

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  7. Understanding the gut microbiota and sarcopenia: a systematic review.Journal of cachexia, sarcopenia and muscle · 2021
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143 more citing papers are in PubMed but not listed here.

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 1 country.

Michael E WalshDepartment of Cellular and Structural Biology, San Antonio, TX, 78229.
Arunabh BhattacharyaDepartment of Cellular and Structural Biology, San Antonio, TX, 78229.
Kavithalakshmi SataranatarajanOklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Rizwan QaisarOklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Lauren SloaneThe Barshop Institute for Longevity and Aging Studies, San Antonio, TX 78245, The University of Texas Health Science Center at San Antonio, TX, 78229, USA.
Md M RahmanDepartment of Cellular and Structural Biology, San Antonio, TX, 78229.
Michael KinterOklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Holly Van RemmenOklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Oklahoma Medical Research Foundation · USThe University of Texas Health Science Center at San Antonio · US

Funding

TRAINING GRANT ON THE BIOLOGY OF AGINGT32AG021890 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Erzsebet Kokovay, JAMES FLOYD NELSON · 2003 to 2026
$11.4M
TRANSGENIC ANIMAL CORE SUBCONTRACT WITH UTHSC AT SAN ANTONIOP01AG020591 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI BROOKS, SUSAN V · 2002 to 2014
$10.7M
BLRD VA I01 BX002595NIA NIH HHS P01 AG020591NIA NIH HHS T32 AG021890NIA NIH HHS T32AG021890
6 · The paper itself

Abstract

Sarcopenia, the loss of skeletal muscle mass and function during aging, is a major contributor to disability and frailty in the elderly. Previous studies found a protective effect of reduced histone deacetylase activity in models of neurogenic muscle atrophy. Because loss of muscle mass during aging is associated with loss of motor neuron innervation, we investigated the potential for the histone deacetylase (HDAC) inhibitor butyrate to modulate age-related muscle loss. Consistent with previous studies, we found significant loss of hindlimb muscle mass in 26-month-old C57Bl/6 female mice fed a control diet. Butyrate treatment starting at 16 months of age wholly or partially protected against muscle atrophy in hindlimb muscles. Butyrate increased muscle fiber cross-sectional area and prevented intramuscular fat accumulation in the old mice. In addition to the protective effect on muscle mass, butyrate reduced fat mass and improved glucose metabolism in 26-month-old mice as determined by a glucose tolerance test. Furthermore, butyrate increased markers of mitochondrial biogenesis in skeletal muscle and whole-body oxygen consumption without affecting activity. The increase in mass in butyrate-treated mice was not due to reduced ubiquitin-mediated proteasomal degradation. However, butyrate reduced markers of oxidative stress and apoptosis and altered antioxidant enzyme activity. Our data is the first to show a beneficial effect of butyrate on muscle mass during aging and suggests HDACs contribute to age-related muscle atrophy and may be effective targets for intervention in sarcopenia and age-related metabolic disease.

Indexed as

AgingAnimalsAntioxidantsApoptosisBody WeightButyratesFemaleGlucoseGlucose Tolerance TestHistone Deacetylase InhibitorsHistone DeacetylasesMiceMice, Inbred C57BLMuscle, SkeletalOxidative StressOxygen ConsumptionAntioxidantsButyratesGlucoseHistone Deacetylase InhibitorsHistone Deacetylasesagingbutyratehistone deacetylasemetabolismsarcopeniaskeletal muscle

Identifiers

PMID26290460
PMCPMC4693467
OpenAlexW1833567598

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.