Lavorato Manuela, Gupta Pawan K, Hopkins Philip M, Franzini-Armstrong Clara
Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine , Philadelphia PA, USA.
Malignant Hyperthermia Unit, Leeds Institute of Biomedical and Clinical Sciences, St James's University Hospital , Leeds, UK.
Eur J Transl Myol. 2016 Sep 15;26(4):6105. doi: 10.4081/ejtm.2016.6105.
We have compared the ultrastructure of skeletal muscle biopsies from patients that have survived a [Malignant Hyperthermia, MH] episode and siblings that test positive for MH susceptibility with those from siblings that tested negatives. The aim is to establish whether life long exposure to the MH-related mutation effects may result in subtle abnormalities even in the absence of active episodes and/or clinically detectable deficiencies. Although a specific ultrastructural signature for MH mutants cannot be demonstrated, an MH related pattern of minor alterations does exist. These include the tendency for micro damage to the contractile apparatus and a higher than normal level of mitochondrial abnormalities.
我们比较了经历过恶性高热(MH)发作且存活下来的患者以及对MH易感性检测呈阳性的兄弟姐妹与检测呈阴性的兄弟姐妹的骨骼肌活检超微结构。目的是确定即使在没有活跃发作和/或临床可检测到的缺陷的情况下,长期暴露于与MH相关的突变影响是否会导致细微异常。虽然无法证明MH突变体有特定的超微结构特征,但确实存在与MH相关的轻微改变模式。这些包括收缩装置微损伤的倾向以及线粒体异常水平高于正常。