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Exercise training reverses age-induced diastolic dysfunction and restores coronary microvascular function

机译:运动培训逆转年龄诱导的舒张功能障碍和恢复冠状动脉微血管功能

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The risk for diastolic dysfunction increases with advancing age. Regular exercise training ameliorates age-related diastolic dysfunction; however, the underlying mechanisms have not been identified. We investigated whether (1) microvascular dysfunction contributes to the development of age-related diastolic dysfunction, and (2) initiation of late-life exercise training reverses age-related diastolic and microvascular dysfunction. Young and old rats underwent 10 weeks of exercise training or remained as sedentary, cage-controls. Isovolumic relaxation time (IVRT), early diastolic filling (E/A), myocardial performance index (MPI) and aortic stiffness (pulse wave velocity; PWV) were evaluated before and after exercise training or cage confinement. Coronary blood flow and vasodilatory responses of coronary arterioles were evaluated in all groups at the end of training. In aged sedentary rats, compared to young sedentary rats, a 42% increase in IVRT, a 64% decrease in E/A, and increased aortic stiffness (PWV: 6.36 +/- 0.47 vs. 4.89 +/- 0.41, OSED vs. YSED, P < 0.05) was accompanied by impaired coronary blood flow at rest and during exercise. Endothelium-dependent vasodilatation was impaired in coronary arterioles from aged rats (maximal relaxation to bradykinin: 56.4 +/- 5.1% vs. 75.3 +/- 5.2%, OSED vs. YSED, P < 0.05). After exercise training, IVRT, a measure of active ventricular relaxation, did not differ between old and young rats. In old rats, exercise training reversed the reduction in E/A, reduced aortic stiffness, and eliminated impairment of coronary blood flow responses and endothelium-dependent vasodilatation. Thus, age-related diastolic and microvascular dysfunction are reversed by late-life exercise training. The restorative effect of exercise training on coronary microvascular function may result from improved endothelial function.
机译:对于随着年龄的舒张功能障碍的风险增加。经常运动训练改善与年龄相关的舒张功能障碍;但是,基本的机制尚未确定。我们调查是否(1)微血管功能障碍有助于与年龄相关的舒张功能障碍的发展,以及晚年的运动训练(2)开始逆转年龄相关的舒张和微血管功能障碍。年轻人和老年人大鼠进行10周运动训练或仍然是久坐,笼控制。等容舒张时间(IVRT),早期舒张(E / A),心肌性能指数(MPI)和主动脉刚度(脉搏波速度; PWV)之前和运动训练或笼分娩后进行评价。冠状动脉血流量和冠状小动脉舒血管反应各组在训练结束时进行了评价。老年大鼠久坐,相比年轻久坐大鼠,增加了42%IVRT,在E / A 64%的减少,以及增加主动脉硬度(PWV:6.36 +/- 0.47 4.89对比0.41 +/-,OSED与YSED,P <0.05)在休息和在锻炼期间伴随着冠状动脉血流量降低。内皮依赖性血管舒张在冠状小动脉受损从老年大鼠(最大松弛到血管舒缓激肽:56.4 +/- 5.1%比75.3 +/- 5.2%,相对于OSED YSED,P <0.05)。运动训练后,IVRT,积极心肌松弛的措施,并没有老幼鼠不同。在老年大鼠,运动训练逆转E / A的减少,减少主动脉刚度,和冠脉血流量的反应和内皮依赖性血管舒张消除损害。因此,与年龄相关的舒张和微血管功能障碍是由晚年的运动训练逆转。对冠状动脉微血管功能康复训练对恢复体力的效果可能是由于改善血管内皮功能。

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