4.5 Article

Differential expression of metabolic genes essential for glucose and lipid metabolism in skeletal muscle from spinal cord injured subjects

期刊

JOURNAL OF APPLIED PHYSIOLOGY
卷 110, 期 5, 页码 1204-1210

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.00686.2010

关键词

glycogen storage; oxidation; metabolism; physical inactivity; tetraplegia

资金

  1. Swedish National Center for Research in Sports
  2. Swedish Medical Association
  3. Magnus Bergvall Foundation
  4. Lars Hierta Foundation
  5. Fredrik and Ingrid Thurings Foundation
  6. Tore Nilson Foundation for Medical Research
  7. Ake Wiberg Foundation
  8. Swedish Research Council
  9. European Foundation for the Study of Diabetes
  10. European Research Council
  11. Swedish Diabetes Association
  12. Novo Nordisk Research Foundation
  13. Commission of the European Communities [LSHM-CT-2004-005272 EXGENESIS, LSHMCT-2004-512013 EUGENE2]

向作者/读者索取更多资源

Skeletal muscle plays an important role in the regulation of energy homeostasis; therefore, the ability of skeletal muscle to adapt and alter metabolic gene expression in response to changes in physiological demands is critical for energy balance. Individuals with cervical spinal cord lesions are characterized by tetraplegia, impaired thermoregulation, and altered skeletal muscle morphology. We characterized skeletal muscle metabolic gene expression patterns, as well as protein content, in these individuals to assess the impact of spinal cord injury on critical determinants of skeletal muscle metabolism. Our results demonstrate that mRNA levels and protein expression of skeletal muscle genes essential for glucose storage are reduced, whereas expression of glycolytic genes is reciprocally increased in individuals with spinal cord injury. Furthermore, expression of genes essential for lipid oxidation is coordinately reduced in spinal cord injured subjects, consistent with a marked reduction of mitochondrial proteins. Thus spinal cord injury resulted in a profound and tightly coordinated change in skeletal muscle metabolic gene expression program that is associated with the aberrant metabolic features of the tissue.

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