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首页> 外文期刊>Circulation: An Official Journal of the American Heart Association >Exercise training attenuates MuRF-1 expression in the skeletal muscle of patients with chronic heart failure independent of age: The randomized leipzig exercise intervention in chronic heart failure and aging catabolism study
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Exercise training attenuates MuRF-1 expression in the skeletal muscle of patients with chronic heart failure independent of age: The randomized leipzig exercise intervention in chronic heart failure and aging catabolism study

机译:运动训练减弱与年龄无关的慢性心力衰竭患者骨骼肌中的MuRF-1表达:莱比锡运动干预对慢性心力衰竭和衰老分解代谢的研究

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Background-Muscle wasting occurs in both chronic heart failure (CHF) and normal aging and contributes to exercise intolerance and increased morbidity/mortality. However, the molecular mechanisms of muscle atrophy in CHF and their interaction with aging are still largely unknown. We therefore measured the activation of the ubiquitin-proteasome system and the lysosomal pathway of intracellular proteolysis in muscle biopsies of CHF patients and healthy controls in two age strata and assessed the age-dependent effects of a 4-week endurance training program on the catabolic-anabolic balance. Methods and Results-Sixty CHF patients (30 patients aged ≤55 years, mean age 46±5 years; 30 patients aged ≥65 years, mean age 72±5 years) and 60 healthy controls (30 subjects aged ≤55 years, mean age 50±5 years; 30 subjects aged ≥65 years, mean age 72±4 years) were randomized to 4 weeks of supervised endurance training or to a control group. Before and after the intervention, vastus lateralis muscle biopsies were obtained. The expressions of cathepsin-L and the muscle-specific E3 ligases MuRF-1 and MAFbx were measured by real-time polymerase chain reaction and confirmed by Western blot. At baseline, MuRF-1 expression was significantly higher in CHF patients versus healthy controls (mRNA: 624±59 versus 401±25 relative units; P=0.007). After 4 weeks of exercise training, MuRF-1 mRNA expression was reduced by-32.8% (P=0.02) in CHF patients aged ≤55 years and by-37.0% (P<0.05) in CHF patients aged ≥65 years. Conclusions-MuRF-1, a component of the ubiquitin-proteasome system involved in muscle proteolysis, is increased in the skeletal muscle of patients with heart failure. Exercise training results in reduced MuRF-1 levels, suggesting that it blocks ubiquitin-proteasome system activation and does so in both younger and older CHF patients. Clinical Trial Registration-: URL: http://www.clinicaltrials.gov. Unique identifier: NCT00176319.
机译:背景-肌肉消瘦发生在慢性心力衰竭(CHF)和正常衰老中,并导致运动不耐症和发病率/死亡率增加。然而,CHF肌肉萎缩的分子机制及其与衰老的相互作用仍然未知。因此,我们在两个年龄层的CHF患者和健康对照者的肌肉活检中测量了泛素-蛋白酶体系统的激活和细胞内蛋白水解的溶酶体途径,并评估了4周耐力训练计划对分解代谢期的年龄依赖性影响合成代谢的平衡。方法和结果-60例CHF患者(30例≤55岁,平均年龄46±5岁; 30例≥65岁,平均年龄72±5岁)和60名健康对照者(30例≤55岁,平均年龄) 50±5年; 30名年龄≥65岁,平均年龄为72±4岁的受试者被随机分为4周有监督耐力训练或对照组。干预前后,均行股外侧肌活检。通过实时聚合酶链反应测量组织蛋白酶L和肌肉特异性E3连接酶MuRF-1和MAFbx的表达,并通过Western印迹进行确认。基线时,CHF患者的MuRF-1表达明显高于健康对照组(mRNA:624±59对401±25相对单位; P = 0.007)。经过4周的运动训练,≤55岁的CHF患者的MuRF-1 mRNA表达降低了32.8%(P = 0.02),≥65岁的CHF患者降低了37.0%(P <0.05)。结论:MuRF-1是参与肌肉蛋白水解的泛素-蛋白酶体系统的组成部分,在心力衰竭患者的骨骼肌中有所增加。运动训练导致MuRF-1水平降低,表明它阻止了泛素-蛋白酶体系统的激活,无论是年轻还是年老的CHF患者均如此。临床试验注册-:URL:http://www.clinicaltrials.gov。唯一标识符:NCT00176319。

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