期刊
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
卷 42, 期 1, 页码 41-52出版社
WILEY
DOI: 10.1111/acer.13531
关键词
Ethanol; IGF-1; IRS-1; p70S6K1; p90RSK1; Ubiquitinated Proteins
资金
- Russian Science Foundation (RSF) [14-15-00392]
- IUSM-NW
- Russian Science Foundation [14-15-00392] Funding Source: Russian Science Foundation
BackgroundAnimal studies showed that alcoholic myopathy is characterized by the reduction in myofiber cross-sectional area (CSA) and by impaired anabolic signaling. The goal of this study was to compare changes in CSA and fiber type composition with modifications in anabolic and catabolic signaling pathways at the early stages of alcohol misuse in humans. MethodsSkeletal muscle samples from 7 male patients with chronic alcohol abuse (AL; 47.72.0years old; alcohol misuse duration 7.70.6years) were compared with muscle from a control group of 7 healthy men (C; 39.7 +/- 5.0years old). Biopsies from vastus lateralis muscles were taken and analyzed for the changes in fiber type composition, fiber CSA, and for the alterations in anabolic and catabolic signaling pathways. ResultsAL patients did not have detectable clinical myopathy symptoms or muscle fiber atrophy, but the relative proportion of fast fibers was increased. There was a significant decrease in IGF-1 in plasma and IRS-1 protein content in muscle of AL group. Levels of total and phosphorylated p70S6K1, GSK3, and p90RSK1 were not different between AL and C groups. Muscle of AL patients had increased mRNA expression of HSP70 and HSP90. A marker of anabolic pathway p-4E-BP1 was decreased, while catabolic markers (MuRF-1, MAFbx, ubiquitinated proteins) were increased in AL patients when compared with C group. ConclusionsAt the early stages of alcohol misuse in humans, changes in the regulation of anabolic and catabolic signaling pathways precede the development of skeletal muscle atrophy and manifestation of clinical symptoms of alcoholic myopathy.
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