Integrative Vascular Biology Laboratory, Department of Integrative Physiology, University of Colorado, Boulder, CO 80309, USA.
J Hum Hypertens. 2011 Jan;25(1):57-62. doi: 10.1038/jhh.2010.31. Epub 2010 Mar 25.
Prehypertension is associated with significant damage to the coronary vasculature and increased rates of adverse cardiovascular events. Circulating endothelial progenitor cells (EPCs) are critical to vascular repair and the formation of new blood vessels. We tested the hypothesis that prehypertension is associated with EPC dysfunction. Peripheral blood samples were collected from 83 middle-aged and older adults (51 male and 32 female): 40 normotensive subjects (age 53±2 years; BP 111/74±1/1 mm Hg) and 43 prehypertensive subjects (age 54±2 years; 128/77±1/1 mm Hg). EPCs were isolated from peripheral blood, and EPC colony-forming capacity (colony-forming unit (CFU) assay), migratory activity (Boyden chamber) and apoptotic susceptibility (active caspase-3 concentrations) were determined. There were no significant differences in the number of EPC CFUs (10±2 vs 9±1), EPC migration (1165±82 vs 1120±84 fluorescent units) or active intracellular caspase-3 concentrations (2.7±0.3 vs 2.3±0.2 ng ml⁻¹) between the normotensive and prehypertensive groups. When groups were stratified into low prehypertension (n=27; systolic blood pressure: 120-129 mm Hg) and high prehypertension (n=16; 130-139 mm Hg), it was found that EPCs from the high prehypertensive group produced fewer (∼65%, P<0.05) CFUs compared with the low prehypertensive (4±1 vs 12±2) and normotensive adults. In conclusion, EPC colony-forming capacity is impaired only in prehypertensive adults with systolic BP greater than 130 mm Hg. Prehypertension is not associated with migratory dysfunction or enhanced apoptosis of EPCs.
高血压前期与冠状动脉血管损伤和心血管不良事件发生率增加有关。循环内皮祖细胞(EPC)对血管修复和新血管形成至关重要。我们检验了高血压前期与 EPC 功能障碍有关的假说。从 83 名中老年成年人(51 名男性和 32 名女性)中采集外周血样本:40 名血压正常的受试者(年龄 53±2 岁;血压 111/74±1/1mmHg)和 43 名高血压前期受试者(年龄 54±2 岁;128/77±1/1mmHg)。从外周血中分离 EPC,并测定 EPC 集落形成能力(集落形成单位(CFU)测定)、迁移活性(Boyden 室)和凋亡易感性(活性 caspase-3 浓度)。在 EPC CFU 数量(10±2 与 9±1)、EPC 迁移(1165±82 与 1120±84 荧光单位)或细胞内活性 caspase-3 浓度(2.7±0.3 与 2.3±0.2ng/ml)方面,血压正常组和高血压前期组之间无显著差异。当将两组分为低高血压前期组(n=27;收缩压:120-129mmHg)和高高血压前期组(n=16;130-139mmHg)时,发现高高血压前期组的 EPC 产生的 CFU 较少(约 65%,P<0.05),与低高血压前期(4±1 与 12±2)和血压正常成年人相比。总之,只有收缩压大于 130mmHg 的高血压前期成年人的 EPC 集落形成能力受损。高血压前期与 EPC 迁移功能障碍或凋亡增强无关。