Cargando…

The Akt/mTOR pathway: Data comparing young and aged mice with leucine supplementation at the onset of skeletal muscle regeneration

The data described herein is related to the article “Differential Effects of Leucine Supplementation in Young and Aged Mice at the Onset of Skeletal Muscle Regeneration” [1]. Aging is associated with a decreased ability of skeletal muscle to regenerate following injury. Leucine supplementation has b...

Descripción completa

Detalles Bibliográficos
Autores principales: Perry, Richard A., Brown, Lemuel A., Lee, David E., Brown, Jacob L., Baum, Jamie I., Greene, Nicholas P., Washington, Tyrone A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007548/
https://www.ncbi.nlm.nih.gov/pubmed/27617277
http://dx.doi.org/10.1016/j.dib.2016.08.013
_version_ 1782451237347655680
author Perry, Richard A.
Brown, Lemuel A.
Lee, David E.
Brown, Jacob L.
Baum, Jamie I.
Greene, Nicholas P.
Washington, Tyrone A.
author_facet Perry, Richard A.
Brown, Lemuel A.
Lee, David E.
Brown, Jacob L.
Baum, Jamie I.
Greene, Nicholas P.
Washington, Tyrone A.
author_sort Perry, Richard A.
collection PubMed
description The data described herein is related to the article “Differential Effects of Leucine Supplementation in Young and Aged Mice at the Onset of Skeletal Muscle Regeneration” [1]. Aging is associated with a decreased ability of skeletal muscle to regenerate following injury. Leucine supplementation has been extensively shown, in young subjects, to promote protein synthesis during regeneration; however, the effects of leucine supplementation on the Akt/mTOR pathway in aged mice at the onset of muscle regeneration are not fully elucidated. In this article, we present data on the Akt/mTOR protein synthesis pathway at the onset of muscle regeneration in young and aged C57BL/6J mice that are and are not receiving leucine supplementation. More specifically, protein content of total Akt, mTOR, p70S6K and 4EBP-1 are presented. Additionally, we provide relative (phosphorylated:total) protein content comparisons of these targets as they present themselves in young and aged mice who have neither been injured nor received leucine supplementation. Lastly, markers of atrophy (FoxO1/O3, MuRF-1, Atrogin-1) are also reported in these young and aged control groups.
format Online
Article
Text
id pubmed-5007548
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-50075482016-09-09 The Akt/mTOR pathway: Data comparing young and aged mice with leucine supplementation at the onset of skeletal muscle regeneration Perry, Richard A. Brown, Lemuel A. Lee, David E. Brown, Jacob L. Baum, Jamie I. Greene, Nicholas P. Washington, Tyrone A. Data Brief Data Article The data described herein is related to the article “Differential Effects of Leucine Supplementation in Young and Aged Mice at the Onset of Skeletal Muscle Regeneration” [1]. Aging is associated with a decreased ability of skeletal muscle to regenerate following injury. Leucine supplementation has been extensively shown, in young subjects, to promote protein synthesis during regeneration; however, the effects of leucine supplementation on the Akt/mTOR pathway in aged mice at the onset of muscle regeneration are not fully elucidated. In this article, we present data on the Akt/mTOR protein synthesis pathway at the onset of muscle regeneration in young and aged C57BL/6J mice that are and are not receiving leucine supplementation. More specifically, protein content of total Akt, mTOR, p70S6K and 4EBP-1 are presented. Additionally, we provide relative (phosphorylated:total) protein content comparisons of these targets as they present themselves in young and aged mice who have neither been injured nor received leucine supplementation. Lastly, markers of atrophy (FoxO1/O3, MuRF-1, Atrogin-1) are also reported in these young and aged control groups. Elsevier 2016-08-11 /pmc/articles/PMC5007548/ /pubmed/27617277 http://dx.doi.org/10.1016/j.dib.2016.08.013 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Perry, Richard A.
Brown, Lemuel A.
Lee, David E.
Brown, Jacob L.
Baum, Jamie I.
Greene, Nicholas P.
Washington, Tyrone A.
The Akt/mTOR pathway: Data comparing young and aged mice with leucine supplementation at the onset of skeletal muscle regeneration
title The Akt/mTOR pathway: Data comparing young and aged mice with leucine supplementation at the onset of skeletal muscle regeneration
title_full The Akt/mTOR pathway: Data comparing young and aged mice with leucine supplementation at the onset of skeletal muscle regeneration
title_fullStr The Akt/mTOR pathway: Data comparing young and aged mice with leucine supplementation at the onset of skeletal muscle regeneration
title_full_unstemmed The Akt/mTOR pathway: Data comparing young and aged mice with leucine supplementation at the onset of skeletal muscle regeneration
title_short The Akt/mTOR pathway: Data comparing young and aged mice with leucine supplementation at the onset of skeletal muscle regeneration
title_sort akt/mtor pathway: data comparing young and aged mice with leucine supplementation at the onset of skeletal muscle regeneration
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007548/
https://www.ncbi.nlm.nih.gov/pubmed/27617277
http://dx.doi.org/10.1016/j.dib.2016.08.013
work_keys_str_mv AT perryricharda theaktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT brownlemuela theaktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT leedavide theaktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT brownjacobl theaktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT baumjamiei theaktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT greenenicholasp theaktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT washingtontyronea theaktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT perryricharda aktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT brownlemuela aktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT leedavide aktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT brownjacobl aktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT baumjamiei aktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT greenenicholasp aktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration
AT washingtontyronea aktmtorpathwaydatacomparingyoungandagedmicewithleucinesupplementationattheonsetofskeletalmuscleregeneration