Michael E. DeBakey Institute for Comparative Cardiovascular Science and Biomedical Devices, Texas A&M University, College Station, USA.
Am J Physiol Heart Circ Physiol. 2011 Apr;300(4):H1201-9. doi: 10.1152/ajpheart.00957.2010. Epub 2011 Feb 4.
Exercise training enhances endothelium-dependent coronary vasodilatation, improving perfusion and contractile function of collateral-dependent myocardium. Paradoxically, studies from our laboratory have revealed increased Ca(2+)-dependent basal active tone in collateral-dependent arteries of exercise-trained pigs. In this study, we tested the hypothesis that exercise training enhances agonist-mediated contractile responses of collateral-dependent arteries by promoting Ca(2+) sensitization. Ameroid constrictors were surgically placed around the proximal left circumflex coronary (LCX) artery of female Yucatan miniature pigs. Eight weeks postoperatively, pigs were randomized into sedentary (pen confined) or exercise-training (treadmill run; 5 days/wk; 14 wk) groups. Arteries (∼150 μm luminal diameter) were isolated from the collateral-dependent and nonoccluded (left anterior descending artery supplied) myocardial regions, and measures of contractile tension or simultaneous tension and intracellular free Ca(2+) concentration levels (fura-2) were completed. Exercise training enhanced contractile responses to endothelin-1 in collateral-dependent compared with nonoccluded arteries, an effect that was more pronounced in the presence of nitric oxide synthase inhibition (N(ω)-nitro-l-arginine methyl ester; 100 μM). Contractile responses to endothelin-1 were not altered by coronary occlusion alone. Exercise training produced increased tension at comparable levels of intracellular free Ca(2+) concentration in collateral-dependent compared with nonoccluded arteries, indicative of exercise training-enhanced Ca(2+) sensitization. Inhibition of PKC (calphostin C; 1 μM), but not Rho-kinase (Y-27632, 10 μM; or hydroxyfasudil, 30 μM), abolished the training-enhanced endothelin-1-mediated contractile response. Exercise training also increased sensitivity to the PKC activator phorbol 12,13-dibutyrate in collateral-dependent compared with nonoccluded arteries. Taken together, these data reveal that exercise training enhances endothelin-1-mediated contractile responses in collateral-dependent coronary arteries likely via increased PKC-mediated Ca(2+) sensitization.
运动训练增强了内皮依赖性冠状动脉舒张,改善了侧支依赖心肌的灌注和收缩功能。矛盾的是,我们实验室的研究表明,在经过运动训练的猪的侧支依赖动脉中,存在钙依赖性基础主动张力增加。在这项研究中,我们通过促进钙敏化来检验运动训练增强侧支依赖动脉激动剂介导的收缩反应的假说。用 Ameroid 缩窄器在雌性尤卡坦微型猪的左回旋支冠状动脉(LCX)近端周围进行手术。手术后 8 周,将猪随机分为安静组(围栏限制)或运动训练组(跑步机跑步;5 天/周;14 周)。从侧支依赖区和非闭塞区(左前降支供应)的心肌中分离出动脉(约 150 μm 管腔直径),并完成收缩张力或同时张力和细胞内游离 Ca 2+浓度水平(fura-2)的测量。与非闭塞动脉相比,运动训练增强了内皮素-1在侧支依赖动脉中的收缩反应,在一氧化氮合酶抑制(N(ω)-硝基-L-精氨酸甲酯;100 μM)存在时,这种作用更为明显。单独的冠状动脉闭塞不会改变内皮素-1的收缩反应。与非闭塞动脉相比,运动训练在相当的细胞内游离 Ca 2+浓度水平下产生更大的张力,表明运动训练增强了 Ca 2+敏化。PKC 抑制(calphostin C;1 μM),但不是 Rho 激酶抑制(Y-27632,10 μM;或羟基法舒地尔,30 μM),消除了训练增强的内皮素-1介导的收缩反应。运动训练还增加了 PKC 激活剂佛波醇 12,13-二丁酸在侧支依赖动脉中的敏感性。综上所述,这些数据表明,运动训练增强了侧支依赖冠状动脉中内皮素-1介导的收缩反应,可能是通过增加 PKC 介导的 Ca 2+敏化。