Abstract
Skeletal muscle mass is controlled by myostatin and Akt-dependent signaling on mammalian target of rapamycin (mTOR), glycogen synthase kinase 3β (GSK3β) and forkhead box O (FoxO) pathways, but it is unknown how these pathways are regulated in critically ill human muscle. To describe factors involved in muscle mass regulation, we investigated the phosphorylation and expression of key factors in these protein synthesis and breakdown signaling pathways in thigh skeletal muscle of critically ill intensive care unit (ICU) patients compared with healthy controls.
Original language | English |
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Journal | P L o S One |
Volume | 6 |
Issue number | 3 |
Pages (from-to) | e18090 |
ISSN | 1932-6203 |
DOIs | |
Publication status | Published - 2011 |
Keywords
- Adult
- Aged
- Blotting, Western
- Case-Control Studies
- Critical Illness
- Female
- Humans
- Male
- Middle Aged
- Muscle Proteins
- Muscle, Skeletal
- Protein Biosynthesis
- Reverse Transcriptase Polymerase Chain Reaction
- Signal Transduction