Diehl K J, Weil B R, Greiner J J, Wright K P, Stauffer B L, DeSouza C A
Department of Integrative Physiology, Integrative Vascular Biology Laboratory, University of Colorado, Boulder, CO, USA.
1] Department of Integrative Physiology, Integrative Vascular Biology Laboratory, University of Colorado, Boulder, CO, USA [2] Department of Medicine, University of Colorado, Denver, CO, USA [3] Denver Health Medical Center, Denver, CO, USA.
J Hum Hypertens. 2015 Aug;29(8):468-72. doi: 10.1038/jhh.2014.120. Epub 2015 Jan 8.
Prehypertension (blood pressure (BP) 120-139/80-89 mm Hg) is associated with an increased risk for future atherothrombotic events. Although the mechanisms underlying this elevated risk are not completely understood, one possibility is that prehypertension is associated with impaired endothelial fibrinolytic capacity. We tested the hypothesis that vascular endothelial release of tissue-type plasminogen activator (t-PA) is impaired in prehypertensive men. Net endothelial release of t-PA was determined, in vivo, in response to intrabrachial infusions of bradykinin (12.5, 25, 50 ng per 100 ml tissue per min) and sodium nitroprusside at (1.0, 2.0, 4.0 μg per 100 ml tissue per min) in 42 middle-age and older men: 16 normotensive (BP range: 100-119/57-79 mm Hg); 16 prehypertensive (BP range: 120-139/76-89 mm Hg); and 10 hypertensive (BP range: 140-150/74-100 mm Hg). Net release of t-PA antigen was ~25% lower (P<0.05) in the prehypertensive (-0.9 ± 0.8 to 42.4 ± 5.3 ng per 100 ml tissue per min) compared with the normotensive (0.5 ± 1.0 to 53.9 ± 6.5 ng per 100 ml tissue per min) men. There was no significant difference in t-PA release between the hypertensive (-1.8 ± 1.6 to 40.8 ± 6.6 ng per 100 ml tissue per min) and prehypertensive groups. Sodium nitroprusside did not significantly alter the t-PA release in any group. These data indicate that endothelial t-PA release is diminished in prehypertensive men. Further, the level of impairment in t-PA release seen with clinical hypertension is already apparent in the prehypertensive state. Impaired endothelial fibrinolytic function may underlie the increased atherothrombotic risk associated with BP in the prehypertensive range.
高血压前期(血压(BP)120 - 139/80 - 89 mmHg)与未来发生动脉粥样硬化血栓形成事件的风险增加相关。尽管这种风险升高背后的机制尚未完全明确,但一种可能性是高血压前期与内皮纤维蛋白溶解能力受损有关。我们检验了这样一个假设:高血压前期男性血管内皮组织型纤溶酶原激活物(t - PA)的释放受损。在42名中老年男性中,通过肱动脉内输注缓激肽(每分钟每100 ml组织12.5、25、50 ng)和硝普钠(每分钟每100 ml组织1.0、2.0、4.0 μg),在体内测定t - PA的净内皮释放量。这42名男性中,16名血压正常(血压范围:100 - 119/57 - 79 mmHg);16名处于高血压前期(血压范围:120 - 139/76 - 89 mmHg);10名患有高血压(血压范围:140 - 150/74 - 100 mmHg)。与血压正常的男性(每分钟每100 ml组织0.5 ± 1.0至53.9 ± 6.5 ng)相比,高血压前期男性(每分钟每100 ml组织 - 0.9 ± 0.8至42.4 ± 5.3 ng)的t - PA抗原净释放量低约25%(P<0.05)。高血压组(每分钟每100 ml组织 - 1.8 ± 1.6至40.8 ± 6.6 ng)和高血压前期组之间的t - PA释放量无显著差异。硝普钠在任何组中均未显著改变t - PA的释放。这些数据表明,高血压前期男性内皮t - PA释放减少。此外,临床高血压时所见的t - PA释放受损水平在高血压前期状态下就已明显。内皮纤维蛋白溶解功能受损可能是高血压前期范围内血压相关的动脉粥样硬化血栓形成风险增加的基础。