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Mechanisms of Atrophy and Myosin Heavy Chain Co-expression in Aging Muscle.

机译:衰老肌肉萎缩和肌球蛋白重链共表达的机制。

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摘要

Sarcopenia is the age related loss of skeletal muscle mass and skeletal muscle function. It causes impairment of mobility activities and can lead to reduced quality of life of elderly persons. Currently, the cause of sarcopenia is unknown and there are no effective methods for its treatment. Recent findings from our lab implicate denervation as the primary instigator of myofiber atrophy leading to the loss of skeletal muscle mass observed in sarcopenia. Using immunolabelling for MuRF1, MHCs and MHCf protein expression, we examined the involvement of the proteasomal protein degradation system in sarcopenia in the context of denervation, as well as the morphology of sarcopenic muscles of different myofiber type compositions. We found that MuRF1 expression was elevated in a denervation specific manner in sarcopenia, that sarcopenic muscle is characterised by marked MHC co-expression and muscle specific shifts in MHC expression, and that MHCs myofibers are not protected from atrophy.
机译:肌肉减少症是与年龄有关的骨骼肌质量和骨骼肌功能丧失。它会导致行动不便,并可能导致老年人的生活质量下降。目前,肌肉减少症的病因尚不清楚,目前尚无有效的治疗方法。我们实验室的最新发现表明,去神经支配是肌纤维萎缩的主要诱因,导致肌少肌症中观察到的骨骼肌质量下降。使用MuRF1,MHCs和MHCf蛋白表达的免疫标记,我们检查了神经变性过程中蛋白酶体蛋白降解系统在肌肉减少症中的参与,以及不同肌纤维类型组成的肌肉减少症的形态。我们发现肌肉减少症中MuRF1的表达以去神经特异性的方式升高,肌肉减少症的特征是MHC共表达和MHC表达中的肌肉特异性移位,并且MHC的肌纤维不受萎缩的保护。

著录项

  • 作者单位

    University of Calgary (Canada).;

  • 授予单位 University of Calgary (Canada).;
  • 学科 Health Sciences Recreation.;Biology Physiology.
  • 学位 M.Sc.
  • 年度 2011
  • 页码 104 p.
  • 总页数 104
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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