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特发性肺动脉高压中的骨骼肌功能障碍。

Skeletal muscle dysfunction in idiopathic pulmonary arterial hypertension.

机构信息

1 Keenan Research Center, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada; and.

出版信息

Am J Respir Cell Mol Biol. 2014 Jan;50(1):74-86. doi: 10.1165/rcmb.2012-0506OC.

Abstract

Despite improvements in survival with disease-targeted therapies, the majority of patients with pulmonary arterial hypertension (PAH) have persistent exercise intolerance that results from impaired cardiac function and skeletal muscle dysfunction. Our intent was to understand the molecular mechanisms mediating skeletal muscle dysfunction in PAH. A total of 12 patients with PAH and 10 matched control subjects were assessed. Patients with PAH demonstrated diminished exercise capacity (lower oxygen uptake max, lower anaerobic threshold and higher minute ventilation/CO2) compared with control subjects. Quadriceps muscle cross-sectional area was significantly smaller in patients with PAH. The vastus lateralis muscle was biopsied to enable muscle fiber morphometric assessment and to determine expression levels/activation of proteins regulating (1) muscle mass, (2) mitochondria biogenesis and shaping machinery, and (3) excitation-contraction coupling. Patients with PAH demonstrated a decreased type I/type II muscle fiber ratio, with a smaller cross-sectional area in the type I fibers. Diminished AKT and p70S6 kinase phosphorylation, with increased atrogin-1 and muscle RING-finger protein-1 transcript levels, were evident in the PAH muscle, suggesting engagement of cellular signaling networks stimulating ubiquitin-proteasome-mediated proteolysis of muscle, with concurrent depression of networks mediating muscle hypertrophy. Although there were no differences in expression/activation of proteins associated with mitochondrial biogenesis or fission (MTCO2 [cytochrome C oxidase subunit II]/succinate dehydrogenase flavoprotein subunit A, mitochondrial transcription factor A, nuclear respiratory factor-1/dynamin-related protein 1 phosphorylation), protein levels of a positive regulator of mitochondrial fusion, Mitofusin2, were significantly lower in patients with PAH. Patients with PAH demonstrated increased phosphorylation of ryanodine receptor 1 receptors, suggesting that altered sarcoplasmic reticulum Ca(++) sequestration may impair excitation-contraction coupling in the PAH muscle. These data suggest that muscle dysfunction in PAH results from a combination of muscle atrophy and intrinsically impaired contractility.

摘要

尽管针对疾病的靶向治疗提高了生存率,但大多数肺动脉高压(PAH)患者仍存在运动耐力持续受损的问题,这是由心功能障碍和骨骼肌功能障碍引起的。我们的目的是了解介导 PAH 骨骼肌功能障碍的分子机制。共评估了 12 名 PAH 患者和 10 名匹配的对照者。与对照组相比,PAH 患者的运动能力明显降低(更低的最大耗氧量、更低的无氧阈值和更高的分钟通气量/CO2)。PAH 患者的股四头肌横截面积明显较小。对股外侧肌进行活检,以进行肌肉纤维形态计量评估,并确定调节(1)肌肉质量、(2)线粒体生物发生和成形机制以及(3)兴奋-收缩偶联的蛋白质的表达水平/激活。PAH 患者的 I 型/II 型肌纤维比例降低,I 型纤维的横截面积更小。PAH 肌肉中的 AKT 和 p70S6 激酶磷酸化减少,而 atrogin-1 和肌肉 RING 指蛋白-1 转录本水平增加,提示参与刺激肌球蛋白体蛋白酶体介导的蛋白水解的细胞信号网络,同时抑制介导肌肉肥大的网络。尽管与线粒体生物发生或分裂相关的蛋白质的表达/激活(MTCO2[细胞色素 C 氧化酶亚基 II]/琥珀酸脱氢酶黄素蛋白亚单位 A、线粒体转录因子 A、核呼吸因子-1/动力相关蛋白 1 磷酸化)没有差异,但线粒体融合的正调节剂 Mitofusin2 的蛋白质水平在 PAH 患者中明显降低。PAH 患者的肌球蛋白受体 1 受体磷酸化增加,提示肌浆网 Ca(++)摄取异常可能损害 PAH 肌肉的兴奋-收缩偶联。这些数据表明,PAH 中的肌肉功能障碍是由肌肉萎缩和固有收缩功能障碍共同引起的。

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