Rich Mark M, Pinter Martin J
Department of Neurology, Emory University School of Medicine, Atlanta, GA 30322, USA.
J Physiol. 2003 Mar 1;547(Pt 2):555-66. doi: 10.1113/jphysiol.2002.035188. Epub 2003 Jan 24.
Critical illness myopathy is an acquired disorder in which skeletal muscle becomes electrically inexcitable. We previously demonstrated that inactivation of Na+ channels contributes to inexcitability of affected fibres in an animal model of critical illness myopathy in which denervated rat skeletal muscle is treated with corticosteroids (steroid denervated; SD). Our previous work, however, did not address the relative importance of membrane depolarization versus a shift in the voltage dependence of fast inactivation in causing inexcitability. It also remained unknown whether changes in the voltage dependence of activation or slow inactivation play a role in inexcitability. In the current study we found that a hyperpolarizing shift in the voltage dependence of fast inactivation of Na+ channels is the principal factor underlying inexcitability in SD fibres. Although depolarization tends to decrease excitability, it is insufficient to account for inexcitability in SD fibres since many normal and denervated fibres retain normal excitability when depolarized to the same resting potentials as affected SD fibres. Changes in the voltage dependence of activation and slow inactivation of Na+ channels were also observed in SD fibres; however, the changes appear to increase rather than decrease excitability. These results highlight the importance of the change in fast inactivation in causing inexcitability of SD fibres.
危重病性肌病是一种获得性疾病,其中骨骼肌变得电不可兴奋。我们先前证明,在危重病性肌病的动物模型中,Na+通道失活导致受影响纤维的不可兴奋性,在该模型中,去神经支配的大鼠骨骼肌用皮质类固醇治疗(类固醇去神经支配;SD)。然而,我们之前的工作没有解决膜去极化与快速失活电压依赖性的改变在导致不可兴奋性方面的相对重要性。激活或缓慢失活电压依赖性的变化是否在不可兴奋性中起作用也仍然未知。在当前研究中,我们发现Na+通道快速失活电压依赖性的超极化偏移是SD纤维不可兴奋性的主要潜在因素。尽管去极化倾向于降低兴奋性,但它不足以解释SD纤维中的不可兴奋性,因为许多正常和去神经支配的纤维在去极化到与受影响的SD纤维相同的静息电位时仍保持正常兴奋性。在SD纤维中也观察到Na+通道激活和缓慢失活电压依赖性的变化;然而,这些变化似乎增加而不是降低兴奋性。这些结果突出了快速失活变化在导致SD纤维不可兴奋性方面的重要性。