[Translocation of MuRF isoforms to nuclei in postural muscle during gravitational unloading].

Ubiquitin-proteasomal proteolytic pathway is one of the key signaling pathways determining protein degradation in muscle fibers. Among the E3 ubiquitin ligases, rate limiting enzymes of the ubiquitin-proteasomal pathway, the most interesting ones are the MuRF isoforms: MuRF-1 and MuRF-2. There are some pieces of evidence that these enzymes are also involved in the regulation of gene expression in skeletal muscle under some specific conditions (i.

[Neuronal NO-synthase as the molecular guard of myofiber stability. NO-dependent signaling pathways in the active and unloaded muscle].

The review is dedicated to the signaling pathways triggered by the nitric oxide II in skeletal muscle. Analysis of the current literature shows that during physical exercise of various intensity and regimen the nitric oxide is an essential trigger of the signaling pathways, leading to the alteration of the structural and metabolic myofiber profile and enhancement of its functional capacity. At the same time during the elevated muscle contractile activity (for instance, eccentric activity), NO serves as a protective and stabilizing agent, preventing from the intensification of the proteolytic processes.

[Effect of 30-day space flight and subsequent readaptation on the signaling processes in m. longissimus dorsi of mice].

Some steps of anabolic and catabolic signaling pathways were investigated in postural/tonic m. longissimus dorsi of mice following the 30-day orbital flight of biosatellite "Bion-M1" and 8-day recovery. Western blotting was used for determining insulin receptor substrate 1 (IRS-1) and AMR-activated protein kinase (AMPK) involved in reciprocal regulation of anabolic and catabolic pathways, as well as E3-ligase MURF-1, and elongation factor eEF2.

[Proteolytic signaling mechanisms in skeletal muscles in patients with alcohol-induced muscle disease].

Chronic alcoholic myopathy is one of most numerous and profound manifestations of chronic alcohol intoxication. This disease is characterized by the pronounced atrophy of the locomotor muscles, which involves predominantly those fibers expressing myosin isoforms of the I "fast" type. In early experiments with alcohol-fed rats and studies of patients it was shown the impairment of the anabolic intracellular signaling pathways and decrease in protein synthesis rate.

[Expression of splice-variants of the insulin-like growth factor I and the condition of the cell-myosatellite pool in the rat m. soleus under conditions of gravitation relief and passive stretching].

We suggested that satellite proliferation with subsequent incorporation of their nuclei in the fibres was essential for enhancement of the protein synthesis in the rat relieved m. soleus. In passive stretch of the muscle, the number of labelled cells exceeded 2.