德菲扎科特
肌发生
杜氏肌营养不良
mdx鼠标
医学
强的松
内分泌学
内科学
振膜(声学)
肌营养不良
骨骼肌
解剖
肌营养不良蛋白
声学
物理
扬声器
作者
Judy E. Anderson,Laura McIntosh,Robert Poettcker
出处
期刊:Muscle & Nerve
[Wiley]
日期:1996-12-01
卷期号:19 (12): 1576-1585
被引量:75
标识
DOI:10.1002/(sici)1097-4598(199612)19:12<1576::aid-mus7>3.0.co;2-7
摘要
The effects of the glucocorticoids deflazacort and prednisone on mdx mouse dystrophy and muscle regeneration were evaluated in a 4.5-week double-blind study to test whether they would decrease dystrophy by anti-inflammatory effects [in intact diaphragm and left tibialis anterior (TA) muscle] and increase new muscle formation (after crush injury). In the left TA, fiber diameter was greater after deflazacort and prednisone compared to placebo. However, only deflazacort increased the centronucleation index of accumulated damage and repair, and myotube growth over the long term. In crush-injured TA, the fusion of proliferative muscle precursors to myotubes (by autoradiography) was increased only after deflazacort. Diaphragm muscle was much less inflamed, and fiber diameter was greater after deflazacort. Results suggest that glucocorticoids decreased the severe phenotype of dystrophy in the mdx diaphragm. Moreover, deflazacort uniquely promoted myogenic repair over short and longer terms, in addition to stimulating fiber growth. These first clues to the targets of deflazacort action on muscle repair have important positive implications for treating Duchenne dystrophy. © 1996 John Wiley & Sons, Inc.
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