首页> 美国卫生研究院文献>American Journal of Physiology - Heart and Circulatory Physiology >Low-intensity aerobic interval training attenuates pathological left ventricular remodeling and mitochondrial dysfunction in aortic-banded miniature swine
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Low-intensity aerobic interval training attenuates pathological left ventricular remodeling and mitochondrial dysfunction in aortic-banded miniature swine

机译:低强度有氧间歇训练可减轻主动脉带小型猪的病理性左心室重塑和线粒体功能障碍

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摘要

Cardiac hypertrophy in response to hypertension or myocardial infarction is a pathological indicator associated with heart failure (HF). A central component of the remodeling process is the loss of cardiomyocytes via cell death pathways regulated by the mitochondrion. Recent evidence has indicated that exercise training can attenuate or reverse pathological remodeling, creating a physiological phenotype. The purpose of this study was to examine left ventricular (LV) function, remodeling, and cardiomyocyte mitochondrial function in aortic-banded (AB) sedentary (HFSED; n = 6), AB exercise-trained (HFTR, n = 5), and control sedentary (n = 5) male Yucatan miniature swine. LV hypertrophy was present in both AB groups before the start of training, as indicated by increases in LV end-diastolic volume, LV end-systolic volume (LVESV), and LV end-systolic dimension (LVESD). Exercise training (15 wk) prevented further increases in LVESV and LVESD (P < 0.05). The heart weight-to-body weight ratio, LV + septum-to-body weight ratio, LV + septum-to-right ventricle ratio, and cardiomyocyte cross-sectional area were increased in both AB groups postmortem regardless of training status. Preservation of LV function after exercise training, as indicated by the maintenance of fractional shortening, ejection fraction, and mean wall shortening and increased stroke volume, was associated with an attenuation of the increased LV fibrosis (23%) and collagen (36%) observed in HFSED animals. LV mitochondrial dysfunction, as measured by Ca2+-induced mitochondrial permeability transition, was increased in HFSED (P < 0.05) but not HFTR animals. In conclusion, low-intensity interval exercise training preserved LV function as exemplified by an attenuation of fibrosis, maintenance of a positive inotropic state, and inhibition of mitochondrial dysfunction, providing further evidence of the therapeutic potential of exercise in a clinical setting.
机译:对高血压或心肌梗塞有反应的心脏肥大是与心力衰竭(HF)相关的病理指标。重塑过程的主要组成部分是通过线粒体调节的细胞死亡途径使心肌细胞损失。最近的证据表明,运动训练可以减弱或逆转病理重塑,从而形成生理表型。这项研究的目的是检查主动脉带(AB)久坐(HFSED; n = 6),AB运动训练(HFTR,n = 5)的久坐患者的左心室(LV)功能,重塑和心肌线粒体功能对照久坐(n = 5)的雄性尤卡坦微型猪。训练开始之前,两个AB组均存在LV肥大,如LV舒张末期容积,LV收缩末期容积(LVESV)和LV收缩末期体积(LVESD)增加所表明。运动训练(15周)可防止LVESV和LVESD进一步升高(P <0.05)。无论训练状态如何,两组AB死后的心脏重量与体重之比,LV +隔膜与体重之比,LV +隔膜与右心室之比以及心肌细胞横截面积均增加。运动训练后LV功能的保持(如缩短分数,射血分数和平均壁缩短和中风量的维持)表明,LV纤维化增加(23%)和胶原蛋白(36%)减轻在HFSED动物中。 Ca 2+ 诱导的线粒体通透性转变,LV线粒体功能障碍在HFSED中增加(P <0.05),但在HFTR动物中则没有。总之,低强度间歇运动训练保留了LV功能,例如减轻纤维化,维持正性肌力状态和抑制线粒体功能障碍,这为临床上运动疗法的治疗潜力提供了进一步的证据。

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