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Alterations in vasomotor control of coronary resistance vessels in remodelled myocardium of swine with a recent myocardial infarction

机译:猪心肌梗死后重塑心肌中冠状动脉阻力血管舒缩控制的改变

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摘要

The mechanism underlying the progressive deterioration of left ventricular (LV) dysfunction after myocardial infarction (MI) towards overt heart failure remains incompletely understood, but may involve impairments in coronary blood flow regulation within remodelled myocardium leading to intermittent myocardial ischemia. Blood flow to the remodelled myocardium is hampered as the coronary vasculature does not grow commensurate with the increase in LV mass and because extravascular compression of the coronary vasculature is increased. In addition to these factors, an increase in coronary vasomotor tone, secondary to neurohumoral activation and endothelial dysfunction, could also contribute to the impaired myocardial oxygen supply. Consequently, we explored, in a series of studies, the alterations in regulation of coronary resistance vessel tone in remodelled myocardium of swine with a 2 to 3-week-old MI. These studies indicate that myocardial oxygen balance is perturbed in remodelled myocardium, thereby forcing the myocardium to increase its oxygen extraction. These perturbations do not appear to be the result of blunted β-adrenergic or endothelial NO-mediated coronary vasodilator influences, and are opposed by an increased vasodilator influence through opening of KATP channels. Unexpectedly, we observed that despite increased circulating levels of noradrenaline, angiotensin II and endothelin-1, α-adrenergic tone remained negligible, while the coronary vasoconstrictor influences of endogenous endothelin and angiotensin II were virtually abolished. We conclude that, early after MI, perturbations in myocardial oxygen balance are observed in remodelled myocardium. However, adaptive alterations in coronary resistance vessel control, consisting of increased vasodilator influences in conjunction with blunted vasoconstrictor influences, act to minimize the impairments of myocardial oxygen balance.
机译:尚不清楚心肌梗塞(MI)导致明显心力衰竭后左心室(LV)功能逐步恶化的潜在机制,但可能涉及重塑心肌中冠状动脉血流调节的损害,导致间歇性心肌缺血。由于冠状动脉血管的增长与左室重量的增加不相称,并且因为冠状血管的血管外压迫增加,阻碍了流向重塑心肌的血流。除这些因素外,继发于神经体液活化和内皮功能障碍的冠状动脉血管舒缩张力增加也可能导致心肌供氧受损。因此,我们在一系列研究中探索了2至3周龄MI的重塑猪心肌中冠状动脉阻力血管张力调节的变化。这些研究表明,心肌氧平衡在改建的心肌中受到干扰,从而迫使心肌增加其氧提取。这些扰动似乎不是β-肾上腺素减弱或内皮NO介导的冠状血管舒张剂影响的结果,而与通过打开KATP通道增加的血管舒张剂影响相反。出乎意料的是,我们观察到,尽管去甲肾上腺素,血管紧张素II和内皮素-1的循环水平增加,但α-肾上腺素的张力仍然可以忽略不计,而内源性内皮素和血管紧张素II的冠状血管收缩作用几乎被消除了。我们得出的结论是,MI后早期,在改建的心肌中观察到了心肌氧平衡的扰动。但是,由增加的血管舒张剂作用和钝化的血管收缩剂作用组成的冠状动脉阻力血管控制的适应性改变可将心肌氧平衡的损害减至最小。

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