Shenkman B S, Tsaturyan A K, Vikhlyantsev I M, Kozlovskaya I B, Grigoriev A I
State Scientific Center of Russian Federation - Institute of Biomedical Problems, Moscow, 123007 Russia.
Lomonosov Moscow State University Research Institute of Mechanics, Moscow, 119192 Russia.
Acta Naturae. 2021 Apr-Jun;13(2):85-97. doi: 10.32607/actanaturae.10953.
Kozlovskaya [1] and Grigoriev [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.
科兹洛夫斯卡娅[1]和格里戈里耶夫[2]表明,早在暴露后的头几天,人类在真实(太空飞行)和模拟微重力条件下就会出现肌肉僵硬(张力缺失)的巨大损失。这种现象归因于慢运动单位的失活,被称为反射性张力缺失。然而,在20世纪末发表了许多证据,表明即使是分离的肌肉或单根纤维也具有相当大的刚度。这种内在刚度由活性成分决定,即在肌肉拉伸和收缩过程中形成肌动蛋白-肌球蛋白横桥的能力,以及由能够抵抗肌肉拉伸的细胞骨架和细胞外基质蛋白决定。本综述考虑了重力卸载条件下肌肉内在刚度的主要事实。分析了在干浸条件下对人类以及对啮齿动物后肢悬吊研究中获得的数据。描述了关于由于肌丝间距增加导致萎缩肌肉中横桥形成概率降低的结果和假设。还讨论了重力卸载过程中细胞骨架蛋白(肌联蛋白、伴肌动蛋白等)降解的证据。介绍了骨骼肌胶原蛋白结构变化的潜在机制及其在降低肌肉内在刚度中的作用。综述了太空飞行和模拟微重力过程中内在刚度变化的分子机制。