Effects of malnutrition with or without eicosapentaenoic acid on proteolytic pathways in diaphragm

被引:4
作者
Bando, Joanne M. [1 ]
Fournier, Mario [1 ]
Da, Xiaoyu [1 ]
Lewis, Michael I. [1 ]
机构
[1] Cedars Sinai Med Ctr, Burns & Allen Res Inst, Div Pulm Crit Care Med, Los Angeles, CA 90048 USA
关键词
FoxO transcription factors; E3; ligases; Muscle fiber atrophy; Calpains; Cathepsins; Myostatin; INTENSIVE-CARE-UNIT; UBIQUITIN-PROTEASOME PATHWAY; SKELETAL-MUSCLE ATROPHY; SHORT-TERM MALNUTRITION; CRITICALLY-ILL PATIENTS; AND/OR GROWTH-HORMONE; MYOSIN HEAVY-CHAIN; PROTEIN-SYNTHESIS; DOWN-REGULATION; NUTRITIONAL SUPPORT;
D O I
10.1016/j.resp.2011.10.003
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Attenuation of muscle wasting has been reported with eicosapentaenoic acid (EPA) use in cachectic states. Pathways mediating muscle proteolysis with severe short-term nutritional deprivation (ND) +/- EPA were evaluated, including diaphragm fiber-specific cross-sectional areas, mRNA (real-time PCR) and protein expression (Western blot). Rats were divided into three groups: (1) free-eating controls, (2) ND and (3) ND + EPA. ND significantly influenced multiple proteolytic pathways. EPA significantly reduced mRNA abundances for most genes to control levels with ND. However, discordant muscle protein expression of many genes was noted with the use of EPA, as protein levels failed to fall. EPA had no impact on diaphragm muscle atrophy, despite the impressive mRNA and some protein results. We conclude that EPA does not attenuate diaphragm muscle atrophy with severe levels of ND. Postulated mechanisms include reduction in muscle protein synthesis and persistent ongoing stimuli for proteolysis. Our study provides unique data on proteolytic signals with ND and has important implications for future studies using EPA. (C) 2011 Elsevier By. All rights reserved.
引用
收藏
页码:14 / 24
页数:11
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