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

被引:11
|
作者
Perry, Richard A., Jr. [1 ]
Brown, Lemuel A. [1 ]
Lee, David E. [1 ]
Brown, Jacob L. [1 ]
Baum, Jamie I. [2 ]
Greene, Nicholas P. [1 ]
Washington, Tyrone A. [1 ]
机构
[1] Univ Arkansas, Dept Hlth Human Performance & Recreat, Fayetteville, AR 72701 USA
[2] Univ Arkansas, Dept Food Sci, Fayetteville, AR 72703 USA
来源
DATA IN BRIEF | 2016年 / 8卷
关键词
MTOR; Skeletal muscle; Regeneration; Leucine supplementation; Aging;
D O I
10.1016/j.dib.2016.08.013
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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/61 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 (Fox01/03, MuRF-1, Atrogin-1) are also reported in these young and aged control groups. (C) 2016 The Authors. Published by Elsevier Inc.
引用
收藏
页码:1426 / 1432
页数:7
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