Moien-Afshari Farzad, Ghosh Sanjoy, Elmi Shahrzad, Khazaei Majid, Rahman Mohammad M, Sallam Nada, Laher Ismail
Department of Pharmacology and Therapeutics, Faculty of Medicine,University of British Columbia, Vancouver, British Columbia, Canada.
Am J Physiol Heart Circ Physiol. 2008 Oct;295(4):H1470-80. doi: 10.1152/ajpheart.00016.2008. Epub 2008 Jul 18.
Regulation of coronary function in diabetic hearts is an important component in preventing ischemic cardiac events but remains poorly studied. Exercise is recommended in the management of diabetes, but its effects on diabetic coronary function are relatively unknown. We investigated coronary artery myogenic tone and endothelial function, essential elements in maintaining vascular fluid dynamics in the myocardium. We hypothesized that exercise reduces pressure-induced myogenic constriction of coronary arteries while improving endothelial function in db/db mice, a model of type 2 diabetes. We used pressurized mouse coronary arteries isolated from hearts of control and db/db mice that were sedentary or exercised for 1 h/day on a motorized exercise-wheel system (set at 5.2 m/day, 5 days/wk). Exercise caused a approximately 10% weight loss in db/db mice and decreased whole body oxidative stress, as measured by plasma 8-isoprostane levels, but failed to improve hyperglycemia or plasma insulin levels. Exercise did not alter myogenic regulation of arterial diameter stimulated by increased transmural pressure, nor did it alter smooth muscle responses to U-46619 (a thromboxane agonist) or sodium nitroprusside (an endothelium-independent dilator). Moderate levels of exercise restored ACh-simulated, endothelium-dependent coronary artery vasodilation in db/db mice and increased expression of Mn SOD and decreased nitrotyrosine levels in hearts of db/db mice. We conclude that the vascular benefits of moderate levels of exercise were independent of changes in myogenic tone or hyperglycemic status and primarily involved increased nitric oxide bioavailability in the coronary microcirculation.
糖尿病心脏中冠状动脉功能的调节是预防缺血性心脏事件的重要组成部分,但目前仍研究不足。糖尿病管理中推荐进行运动,但其对糖尿病冠状动脉功能的影响相对未知。我们研究了冠状动脉肌源性张力和内皮功能,这是维持心肌血管流体动力学的关键要素。我们假设运动可减轻压力诱导的糖尿病小鼠(2型糖尿病模型)冠状动脉肌源性收缩,同时改善内皮功能。我们使用从对照小鼠和糖尿病小鼠心脏分离的加压小鼠冠状动脉,这些小鼠要么久坐不动,要么在电动运动轮系统上每天运动1小时(设定为每天5.2米,每周5天)。运动使糖尿病小鼠体重减轻约10%,并降低了全身氧化应激(通过血浆8-异前列腺素水平测量),但未能改善高血糖或血浆胰岛素水平。运动并未改变跨壁压力增加所刺激的动脉直径的肌源性调节,也未改变平滑肌对U-46619(一种血栓素激动剂)或硝普钠(一种不依赖内皮的扩张剂)的反应。适度运动恢复了糖尿病小鼠中乙酰胆碱刺激的、依赖内皮的冠状动脉血管舒张,并增加了锰超氧化物歧化酶的表达,降低了糖尿病小鼠心脏中的硝基酪氨酸水平。我们得出结论,适度运动对血管的益处独立于肌源性张力或高血糖状态的变化,主要涉及冠状动脉微循环中一氧化氮生物利用度的增加。