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Endurance exercise training in pulmonary hypertension increases skeletal muscle electron transport chain supercomplex assembly

机译:肺动脉高压耐力运动训练增加骨骼肌电子传输链超级复杂组件

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摘要

Pulmonary hypertension is associated with pronounced exercise intolerance (decreased V ċ O2 max) that can significantly impact quality of life. The cause of exercise intolerance in pulmonary hypertension remains unclear. Mitochondrial supercomplexes are large respiratory assemblies of individual electron transport chain complexes which can promote more efficient respiration. In this study, we examined pulmonary hypertension and exercise-induced changes in skeletal muscle electron transport chain protein expression and supercomplex assembly. Pulmonary arterial hypertension was induced in rats with the Sugen/Hypoxia model (10% FiO2, three weeks). Pulmonary arterial hypertension and control rats were assigned to an exercise training protocol group or kept sedentary for one month. Cardiac function and V ċ O2 max were assessed at the beginning and end of exercise training. Red (Type 1—oxidative muscle) and white (Type 2—glycolytic muscle) gastrocnemius were assessed for changes in electron transport chain complex protein expression and supercomplex assembly via SDS- and Blue Native-PAGE. Results showed that pulmonary arterial hypertension caused a significant decrease in V ċ O2 max via treadmill testing that was improved with exercise (P < 0.01). Decreases in cardiac output and pulmonary acceleration time due to pulmonary arterial hypertension were not improved with exercise. Pulmonary arterial hypertension reduced expression in individual electron transport chain complex protein expression (NDUFB8 (CI), SDHB (CII), Cox IV (CIV), but not UQCRC2 (CIII), or ATP5a (CV)) in red gastrocnemius muscle. Both red gastrocnemius and white gastrocnemius electron transport chain expression was unaffected by exercise. However, non-denaturing Blue Native-PAGE analysis of mitochondrial supercomplexes demonstrated increases with exercise training in pulmonary arterial hypertension in the red gastrocnemius but not white gastrocnemius muscle. Pulmonary arterial hypertension-induced exercise intolerance is improved with exercise and is associated with muscle type specific alteration in mitochondrial supercomplex assembly and expression of mitochondrial electron transport chain proteins.
机译:肺动脉高压与明显的运动不耐受(降低V≠O2最大)有关,可以显着影响生活质量。肺动脉高压运动不耐受性的原因仍然不清楚。线粒体超复杂是个体电子传输链复合物的大型呼吸组合物,其可以促进更有效的呼吸。在这项研究中,我们检查了骨骼肌电子传输链蛋白表达和超复杂组件的肺动脉高压和运动诱导的变化。在Sugen /缺氧模型(10%FiO2,3周)中诱导肺动脉高血压。将肺动脉高压和对照大鼠分配给运动培训协议组或保持久坐不持续一个月。在运动培训的开始和结束时评估心功能和VċO2 Max。通过SDS-和蓝色天然页评估红色(类型1-氧化肌肉)和白色(2型糖醛肌肉)胃肠肿瘤肿瘤Memius,用于电子传输链复合蛋白表达和超复杂组件的变化。结果表明,肺动脉高压导致V通过跑步机检测与运动改善的跑步机检测产生显着降低(P <0.01)。随着锻炼没有改善由于肺动脉高血压引起的心输出和肺加速时间的降低。肺动脉高压下的表达在单个电子传送链复合蛋白表达中(NDUFB8(CI),SDHB(CII),COX IV(CII),但不是uQCRC2(CIII),或ATP5A(CV))中的表达中的表达中的红色胃肠肌肌。红色胃内和白色腓肠肌电子传输链表达不受运动的影响。然而,非变性蓝色天然页面对线粒体超复杂的分析表明,红细胞患者肺动脉高血压的运动训练表现出增加,但不是白色的胃肠肌肌肉。肺动脉高压诱导的运动不耐受性具有锻炼,并且与线粒体超复杂组件中的肌肉型特异性改变和线粒体电子传输链蛋白的表达有关。

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