Altered gene expression in steroid-treated denervated muscle

被引:32
作者
Rich, MM
Kraner, SD
Barchi, RL
机构
[1] Emory Univ, Sch Med, Dept Neurol, Atlanta, GA 30322 USA
[2] Univ Penn, Dept Neurosci, Philadelphia, PA 19101 USA
关键词
myopathy; sodium channel; critical illness; denervation; corticosteroid;
D O I
10.1006/nbdi.1999.0257
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In rats treated with high-dose corticosteroids, skeletal muscle that is denervated in vivo (steroid-denervated) develops electrical inexcitability similar to that seen in patients with acute quadriplegic myopathy. To determine whether changes in muscle gene transcription might underlie inexcitability of steroid-denervated muscle we performed RNase protection assays to quantitate adult (SkM1) and embryonic (SkM2) sodium channel isoforms and chloride channel (CLC-1) mRNA levels in control, denervated, steroid-innervated, and steroid-denervated skeletal muscle. While SkM1 mRNA levels were relatively unaffected by denervation or steroid treatment, SkM2 mRNA levels were increased by both. These effects were synergistic and high levels of SkM2 mRNA were expressed in denervated muscle exposed to corticosteroids. Skeletal muscle CLC-1 mRNA levels were decreased by denervation. To better understand the marked upregulation of SkM2 in steroid-denervated muscle we examined changes in myogenin and glucocorticoid receptor mRNA levels. However, changes in these mRNA levels cannot account for the upregulation of SkM2 in steroid-denervated muscle. (C) 1999 Academic Press.
引用
收藏
页码:515 / 522
页数:8
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