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首页> 外文期刊>The Journal of Physiology >Autophagy and mitophagy flux in young and aged skeletal muscle following chronic contractile activity
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Autophagy and mitophagy flux in young and aged skeletal muscle following chronic contractile activity

机译:慢性收缩活动后年轻和老年骨骼肌中的自噬和水肿源

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Key points A healthy mitochondrial pool is dependent on the removal of dysfunctional organelles via mitophagy, but little is known about how mitophagy is altered with ageing and chronic exercise. Chronic contractile activity (CCA) is a standardized exercise model that can elicit mitochondrial adaptations in both young and aged muscle, albeit to a lesser degree in the aged group. Assessment of mitophagy flux revealed enhanced targeting of mitochondria for degradation in aged muscle, in contrast to previous theories. Mitophagy flux was significantly reduced as an adaptation to CCA suggesting that an improvement in organelle quality reduces the need for mitochondrial turnover. CCA enhances lysosomal capacity and may ameliorate lysosomal dysfunction in aged muscle. Abstract Skeletal muscle exhibits deficits in mitochondrial quality with age. Central to the maintenance of a healthy mitochondrial pool is the removal of dysfunctional organelles via mitophagy. Little is known on how mitophagy is altered with ageing and chronic exercise. We assessed mitophagy flux using colchicine treatment in vivo following chronic contractile activity (CCA) of muscle in young and aged rats. CCA evoked mitochondrial biogenesis in young muscle, with an attenuated response in aged muscle. Mitophagy flux was higher in aged muscle and was correlated with the enhanced expression of mitophagy receptors and upstream transcriptional regulators. CCA decreased mitophagy flux in both age groups, suggesting an improvement in organelle quality. CCA also reduced the exaggerated expression of TFEB evident in aged muscle, which may be promoting the age‐induced increase in lysosomal markers. Thus, aged muscle possesses an elevated drive for autophagy and mitophagy which may contribute to the decline in organelle content observed with age, but which may serve to maintain mitochondrial quality. CCA improves organelle integrity and reduces mitophagy, illustrating that chronic exercise is a modality to improve muscle quality in aged populations.
机译:重点是一种健康的线粒体游泳池依赖于通过影响的消除功能障碍细胞器,但很少是众所周知的是,患有老化和慢性运动如何改变。慢性收缩活动(CCA)是一种标准化的运动模型,可以在年轻人和老年肌肉中引出线粒体适应,尽管老年人的较小程度。与以前的理论相比,助殖助焊剂的评估显示了大脑肌肌的降解的增强靶向。随着对CCA的适应性而言,MITOCHAGY FLUX显着降低了表明细胞器质量的改善降低了对线粒体周转的需求。 CCA增强溶酶体能力,可改善老年肌肉的溶酶体功能障碍。摘要骨骼肌呈现出线粒体质量的赤字随着年龄的增长。维持健康线粒体游泳池的核心是通过MITOCHAGY去除功能障碍细胞器。对于患者和慢性运动的改变,众所周知。我们评估了在年轻和老年大鼠肌肉的慢性收缩活动(CCA)后体内使用碎氏菌治疗。 CCA在年轻肌肉中诱发线粒体生物发生,在老年肌肉中具有减毒的反应。肌肉肌肉的肺泡较高,与乳化物受体和上游转录调节因子的增强表达相关。 CCA在两个年龄组中减少了患有的疾病通量,表明细胞器质量的提高。 CCA还减少了在老年肌肉中TFEB明显的夸张表达,这可能促进溶酶体标志物的年龄诱导的增加。因此,老年肌肉具有升高的自噬和水道驱动,这可能有助于随着年龄观察到的细胞器含量的下降,但这可能用于维持线粒体质量。 CCA改善了细胞石完整性并减少了含有的细胞质,说明慢性锻炼是改善老龄化群体中肌肉质量的态度。

著录项

  • 来源
    《The Journal of Physiology》 |2018年第16期|共18页
  • 作者单位

    Muscle Health Research Centre School of Kinesiology and Health ScienceYork UniversityToronto;

    Muscle Health Research Centre School of Kinesiology and Health ScienceYork UniversityToronto;

    Muscle Health Research Centre School of Kinesiology and Health ScienceYork UniversityToronto;

    Muscle Health Research Centre School of Kinesiology and Health ScienceYork UniversityToronto;

    Muscle Health Research Centre School of Kinesiology and Health ScienceYork UniversityToronto;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 人体生理学;
  • 关键词

    mitochondria; exercise; aging;

    机译:线粒体;运动;老龄化;

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