Muscle atrophy is
a deleterious consequence of physical inactivity
and is associated with increased morbidity and mortality. The aim
of this study was to decipher the mechanisms involved in disuse muscle
atrophy in eight healthy men using a 21 day bed rest with a cross-over
design (control, with resistive vibration exercise (RVE), or RVE combined
with whey protein supplementation and an alkaline salt (NEX)). The
main physiological findings show a significant reduction in whole-body
fat-free mass (CON −4.1%, RVE −4.3%, NEX −2.7%, p < 0.05), maximal oxygen consumption (CON −20.5%,
RVE −6.46%, NEX −7.9%, p < 0.05),
and maximal voluntary contraction (CON −15%, RVE −12%,
and NEX −9.5%, p < 0.05) and a reduction
in mitochondrial enzyme activity (CON −30.7%, RVE −31.3%,
NEX −17%, p < 0.05). The benefits of nutrition
and exercise countermeasure were evident with an increase in leg lean
mass (CON −1.7%, RVE +8.9%, NEX +15%, p <
0.05). Changes to the vastus lateralis muscle proteome were characterized
using mass spectrometry-based label-free quantitative proteomics,
the findings of which suggest alterations to cell metabolism, mitochondrial
metabolism, protein synthesis, and degradation pathways during bed
rest. The observed changes were partially mitigated during RVE, but
there were no significant pathway changes during the NEX trial. The
mass spectrometry proteomics data have been deposited to the ProteomeXchange
Consortium with the dataset identifier PXD006882. In conclusion, resistive
vibration exercise, when combined with whey/alkalizing salt supplementation,
could be an effective strategy to prevent skeletal muscle protein
changes, muscle atrophy, and insulin sensitivity during medium duration
bed rest.