Chronic treatment with agents that stabilize cytosolic IκB-α enhances survival and improves resting membrane potential in MDX muscle fibers subjected to chronic passive stretch

被引:35
作者
Carlson, CG [1 ]
Samadi, A [1 ]
Siegel, A [1 ]
机构
[1] AT Still Univ, Kirksville Coll Osteopath Med, Dept Physiol, Kirksville, MO 63501 USA
关键词
Duchenne muscular dystrophy; mdx mouse; dystrophinopathies; NF kappa B; I kappa B-alpha; pyrollidine dithiocarbamate; passive stretch; eccentric muscle contraction; Ca2+ influx; expiratory muscle;
D O I
10.1016/j.nbd.2005.05.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The potential pathogenic role of increased NF kappa B signaling in passively stretched dystrophic skeletal muscle was examined by treating adult mdx mice with an agent that stabilized cytosolic I kappa B-alpha(x (pyrollidine dithiocarbamate, PDTC)and examining the effects of this treatment on the chronically stretched mdx triangularis sterni (TS) muscle. Daily PDTC treatment significantly increased the number of surviving striated TS fibers regardless of age. TS fibers from untreated mdx mice had significantly lower resting potentials (RPs) than nondystrophic mice. Treatment with GdCl3 to block resting Ca2+ influx had no effect on RP in either nondystrophic or mdx preparations. Daily treatment with PDTC significantly improved the RP regardless of age. These results are consistent with the hypothesis that passive stretch activates an NF kappa B-mediated pathogenic mechanism in dystrophic muscle and suggest that agents which stabilize cytosolic l kappa B-alpha levels may be useful for treating Duchenne and related muscular dystrophies. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:719 / 730
页数:12
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