[SIGNALING PATHWAYS INVOLVED IN THE REGULATION OF PROTEIN METABOLISM IN SKELETAL MUSCLE]

Ross Fiziol Zh Im I M Sechenova. 2016 Jul;102(7):753-72.
[Article in Russian]

Abstract

The ability of muscle cells to respond to certain signaling molecules depends on the presence of specific proteins-receptors, ion channels and transporters, which create a system of metabolic inputs. All cells in the human body have a transmembrane signaling system that allows to get information from extracellular stimuli such as hormones, neurotransmitters, proteins, peptides, derivatives of amino acids and fat acids, sensor molecules. The results of researches published in the last two years, which expand knowledge of action of various factors on protein metabolism in skeletal muscles are presented in the review. The main attention is turned to the discovery and expansion of signaling pathways involved in the regulation of protein metabolism in skeletal muscle in different functional states of the person.

Publication types

  • Review

MeSH terms

  • Amino Acids / metabolism
  • Animals
  • Exercise
  • Fatty Acids / metabolism
  • GTP-Binding Proteins / classification
  • GTP-Binding Proteins / genetics
  • GTP-Binding Proteins / metabolism*
  • Gene Expression Regulation
  • Humans
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Ion Channels / genetics
  • Ion Channels / metabolism
  • Muscle Cells / cytology
  • Muscle Cells / metabolism
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Muscle, Skeletal / cytology
  • Muscle, Skeletal / metabolism*
  • Muscular Atrophy / genetics
  • Muscular Atrophy / metabolism*
  • Muscular Atrophy / pathology
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Signal Transduction*
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • ADGRG1 protein, human
  • Amino Acids
  • Fatty Acids
  • IGF1 protein, human
  • Ion Channels
  • Muscle Proteins
  • Receptors, G-Protein-Coupled
  • Insulin-Like Growth Factor I
  • MTOR protein, human
  • TOR Serine-Threonine Kinases
  • GTP-Binding Proteins