Dept. of Biomedical Science, Univ. of Missouri, 1600 E. Rollins, E117 Veterinary Medicine, Columbia, MO 65211, USA.
Am J Physiol Heart Circ Physiol. 2010 Nov;299(5):H1348-56. doi: 10.1152/ajpheart.00578.2010. Epub 2010 Sep 3.
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 Ca(2+)-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.
高血压或心肌梗死引起的心肌肥厚是心力衰竭(HF)相关的病理指标。重塑过程的一个核心组成部分是通过线粒体调节的细胞死亡途径导致心肌细胞丧失。最近的证据表明,运动训练可以减轻或逆转病理性重塑,产生生理表型。本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)和对照久坐(n = 5)雄性尤卡坦小型猪的左心室(LV)功能、重塑和心肌细胞线粒体功能。LV 肥大在 AB 两组中都存在,这表明 LV 舒张末期容积、LV 收缩末期容积(LVESV)和 LV 收缩末期直径(LVESD)增加。运动训练(15 周)阻止了 LVESV 和 LVESD 的进一步增加(P < 0.05)。无论训练状态如何,AB 两组的心脏重量与体重比、LV + 室间隔与体重比、LV + 室间隔与右心室比和心肌细胞横截面积在死后均增加。运动训练后 LV 功能的保持,如分数缩短、射血分数、平均壁缩短和增加的每搏量的保持,与观察到的 HFSED 动物中 LV 纤维化(23%)和胶原蛋白(36%)的增加减弱有关。LV 线粒体功能障碍,如 Ca(2+)诱导的线粒体通透性转换所测量的,在 HFSED 中增加(P < 0.05),但在 HFTR 中没有增加。总之,低强度间歇运动训练保持了 LV 功能,如纤维化减弱、正性肌力状态的维持和线粒体功能障碍的抑制,为运动在临床环境中的治疗潜力提供了进一步的证据。