Literature DB >> 34298968

Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype.

Elena Ignatieva1, Natalia Smolina1, Anna Kostareva1,2, Renata Dmitrieva1.   

Abstract

Mitochondrial dysfunction is considered the major contributor to skeletal muscle wasting in different conditions. Genetically determined neuromuscular disorders occur as a result of mutations in the structural proteins of striated muscle cells and therefore are often combined with cardiac phenotype, which most often manifests as a cardiomyopathy. The specific roles played by mitochondria and mitochondrial energetic metabolism in skeletal muscle under muscle-wasting conditions in cardiomyopathies have not yet been investigated in detail, and this aspect of genetic muscle diseases remains poorly characterized. This review will highlight dysregulation of mitochondrial representation and bioenergetics in specific skeletal muscle disorders caused by mutations that disrupt the structural and functional integrity of muscle cells.

Entities:  

Keywords:  cardiomyopathies; mitochondrial dysfunction; neuromuscular disorders

Year:  2021        PMID: 34298968     DOI: 10.3390/ijms22147349

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  2 in total

1.  Effect of Alisporivir on Calcium Ion Transport and Mitophagy in Skeletal Muscle and Heart Mitochondria in Dystrophin-Deficient Mice.

Authors:  M V Dubinin; V S Starinets; I B Mikheeva; K N Belosludtsev
Journal:  Bull Exp Biol Med       Date:  2022-05-02       Impact factor: 0.804

2.  Cmarr/miR-540-3p axis promotes cardiomyocyte maturation transition by orchestrating Dtna expression.

Authors:  Yukang Wu; Xudong Guo; Tong Han; Ke Feng; Peng Zhang; Yanxin Xu; Yiwei Yang; Yuchen Xia; Yang Chen; Jiajie Xi; Huangtian Yang; Xiaoping Wan; Jiuhong Kang
Journal:  Mol Ther Nucleic Acids       Date:  2022-07-31       Impact factor: 10.183

  2 in total

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