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Molecular Mechanisms of Muscle Tone Impairment under Conditions of Real and Simulated Space Flight
Author(s) -
Б. С. Шенкман,
Andrey K. Tsaturyan,
Ivan M. Vihlyantsev,
I. B. Kozlovskaya,
Anatoliy I. Grigoriev
Publication year - 2021
Publication title -
acta naturae
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 26
ISSN - 2075-8251
DOI - 10.32607/actanaturae.10953
Subject(s) - titin , myosin , biophysics , cytoskeleton , sarcomere , stiffness , muscle stiffness , skeletal muscle , chemistry , weightlessness , extracellular matrix , muscle contraction , actin , anatomy , materials science , biology , microbiology and biotechnology , physics , myocyte , biochemistry , astronomy , cell , composite material
Kozlovskaya et al. [ 1 ] and Grigoriev et al. [ 2 ] showed that enormous loss of muscle stiffness (atonia) develops in humans under true (space flight) and simulated microgravity conditions as early as after the first days of exposure. This phenomenon is attributed to the inactivation of slow motor units and called reflectory atonia. However, a lot of evidence indicating that even isolated muscle or a single fiber possesses substantial stiffness was published at the end of the 20th century. This intrinsic stiffness is determined by the active component, i.e. the ability to form actin-myosin cross-bridges during muscle stretch and contraction, as well as by cytoskeletal and extracellular matrix proteins, capable of resisting muscle stretch. The main facts on intrinsic muscle stiffness under conditions of gravitational unloading are considered in this review. The data obtained in studies of humans under dry immersion and rodent hindlimb suspension is analyzed. The results and hypotheses regarding reduced probability of cross-bridge formation in an atrophying muscle due to increased interfilament spacing are described. The evidence of cytoskeletal protein (titin, nebulin, etc.) degradation during gravitational unloading is also discussed. The possible mechanisms underlying structural changes in skeletal muscle collagen and its role in reducing intrinsic muscle stiffness are presented. The molecular mechanisms of changes in intrinsic stiffness during space flight and simulated microgravity are reviewed.

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