Pharmacotherapeutic Approaches to Treatment of Muscular Dystrophies

被引:4
|
作者
Rawls, Alan [1 ]
Diviak, Bridget K. [1 ,2 ]
Smith, Cameron I. [1 ,2 ]
Severson, Grant W. [1 ,2 ]
Acosta, Sofia A. [1 ,2 ]
Wilson-Rawls, Jeanne [1 ]
机构
[1] Arizona State Univ, Sch Life Sci, Tempe, AZ 85287 USA
[2] Sch Life Sci, Mol & Cellular Biol Grad Program, Tempe, AZ 85287 USA
关键词
muscular dystrophy; dystrophin; dysferlin; DUX4; dystroglycan; inflammation; fibrosis; sarcoglycan; lamin A; emerin; SKELETAL-MUSCLE REGENERATION; FUKUTIN-RELATED PROTEIN; MOUSE MODEL; MITOCHONDRIAL DYSFUNCTION; DOUBLE-BLIND; PLASMINOGEN ACTIVATION; DILATED CARDIOMYOPATHY; INHIBITION IMPROVES; ALPHA-DYSTROGLYCAN; RECEPTOR BLOCKADE;
D O I
10.3390/biom13101536
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Muscular dystrophies are a heterogeneous group of genetic muscle-wasting disorders that are subdivided based on the region of the body impacted by muscle weakness as well as the functional activity of the underlying genetic mutations. A common feature of the pathophysiology of muscular dystrophies is chronic inflammation associated with the replacement of muscle mass with fibrotic scarring. With the progression of these disorders, many patients suffer cardiomyopathies with fibrosis of the cardiac tissue. Anti-inflammatory glucocorticoids represent the standard of care for Duchenne muscular dystrophy, the most common muscular dystrophy worldwide; however, long-term exposure to glucocorticoids results in highly adverse side effects, limiting their use. Thus, it is important to develop new pharmacotherapeutic approaches to limit inflammation and fibrosis to reduce muscle damage and promote repair. Here, we examine the pathophysiology, genetic background, and emerging therapeutic strategies for muscular dystrophies.
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页数:31
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