Szabó András, Wuytack Frank, Zádor Erno
Institute of Biochemistry, Faculty of General Medicine, University of Szeged, Szeged, Hungary.
J Histochem Cytochem. 2008 Nov;56(11):1013-22. doi: 10.1369/jhc.2008.951632. Epub 2008 Aug 4.
The sarco-endoplasmic reticulum Ca2+ ATP-ase (SERCA) and myosin heavy chain (MyHC) levels were measured in hindlimb-denervated and selectively denervated rat soleus muscles. Selective denervation allowed passive movement of the soleus, whereas hindlimb denervation rendered it to passivity. To minimize chronic effects, we followed the changes only for 2 weeks. Selective denervation resulted in less muscle atrophy, a faster slow-to-fast transition of MyHC isoforms, and less coordinated expressions of the slow vs fast isoforms of MyHC and SERCA. Generally, expression of the slow-twitch type SERCA2a was found to be less dependent, whereas the slow-twitch type MyHC1 was the most dependent on innervation. Our study shows that passive movement is able to ameliorate denervation-induced atrophy of the soleus and that it also accentuates the dyscoordination in the expression of the corresponding slow and fast isoforms of MyHC and SERCA.
在大鼠后肢去神经支配和选择性去神经支配的比目鱼肌中,测量了肌浆网/内质网Ca2+ATP酶(SERCA)和肌球蛋白重链(MyHC)的水平。选择性去神经支配允许比目鱼肌被动运动,而后肢去神经支配则使其完全被动。为了尽量减少慢性影响,我们仅观察了2周内的变化。选择性去神经支配导致较少的肌肉萎缩、MyHC亚型从慢到快的转变更快,以及MyHC和SERCA慢型与快型之间的协同表达减少。一般来说,慢肌型SERCA2a的表达发现较少依赖神经支配,而慢肌型MyHC1对神经支配的依赖性最强。我们的研究表明,被动运动能够改善去神经支配引起的比目鱼肌萎缩,并且还会加剧MyHC和SERCA相应慢型和快型表达的失调。