Nohria Anju, Garrett Leslie, Johnson Wendy, Kinlay Scott, Ganz Peter, Creager Mark A
Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Mass 02115, USA.
Hypertension. 2003 Jul;42(1):43-8. doi: 10.1161/01.HYP.0000074426.71392.D8. Epub 2003 May 19.
Endothelin-1 (ET-1) is a potent vasoconstrictor that increases vascular tone in the resistance vessels of subjects with hypertension. It is unclear whether endogenous ET-1 affects resistance-vessel function equally in patients with other cardiovascular risk factors. Vasoconstriction to ET-1 is mediated principally via the endothelin-A (ETA) receptor on vascular smooth muscle cells. Accordingly, we used an ETA-specific antagonist, BQ-123, to test the hypothesis that endogenous ET-1 increases vascular resistance selectively in subjects with hypertension compared with other risk factors. BQ-123 was infused at 100 nmol/min for 80 minutes into the brachial artery of 10 subjects with hypertension (mean+/-SEM arterial pressure, 106+/-5 mm Hg), 12 subjects with hypercholesterolemia (mean+/-SEM total cholesterol, 7.1+/-0.2 mmol/L), 10 active smokers (mean+/-SEM, 42+/-11 pack-years), and 11 healthy, age-matched individuals. Forearm blood flow (FBF) was measured by venous occlusion plethysmography. BQ-123 dilated resistance arterioles in hypertensive subjects, with FBF's increasing by 46+/-7% from baseline (P<0.001). BQ-123 increased FBF to a lesser extent in hypercholesterolemic (24+/-5%, P<0.001) and healthy (20+/-8%, P=0.007) individuals but did not affect FBF significantly in smokers (10+/-8%, P=0.185). The vasodilator response in hypertensive subjects, but not in hypercholesterolemic patients or smokers, was significantly greater than that in healthy individuals (P=0.012). Endogenous ET-1, acting via the ETA receptor, increases resistance-vessel tone in subjects with hypertension more than in subjects with hypercholesterolemia or in smokers. These results indicate that ET-1 contributes more to the pathophysiology of hypertension than of other risk factors in subjects without overt atherosclerosis.
内皮素 -1(ET -1)是一种强效血管收缩剂,可增加高血压患者阻力血管的血管张力。目前尚不清楚内源性ET -1对其他心血管危险因素患者的阻力血管功能影响是否相同。对ET -1的血管收缩作用主要通过血管平滑肌细胞上的内皮素A(ETA)受体介导。因此,我们使用一种ETA特异性拮抗剂BQ -123来检验以下假设:与其他危险因素相比,内源性ET -1在高血压患者中选择性增加血管阻力。将BQ -123以100 nmol/分钟的速度注入10名高血压患者(平均±标准误动脉压,106±5 mmHg)、12名高胆固醇血症患者(平均±标准误总胆固醇,7.1±0.2 mmol/L)、10名现吸烟者(平均±标准误,42±11包年)和11名健康的、年龄匹配个体的肱动脉中,持续80分钟。通过静脉阻断体积描记法测量前臂血流量(FBF)。BQ -123使高血压患者的阻力小动脉扩张,FBF较基线增加46±7%(P<0.001)。BQ -123在高胆固醇血症患者(24±5%,P<0.001)和健康个体(20±8%,P =(此处原文有误,应是P = 0.007))中使FBF增加的程度较小,但对吸烟者的FBF无显著影响(10±8%,P = 0.185)。高血压患者的血管舒张反应显著大于健康个体(P =(此处原文有误,应是P = 0.012)),而高胆固醇血症患者或吸烟者则不然。通过ETA受体起作用的内源性ET -1增加高血压患者阻力血管张力的程度大于高胆固醇血症患者或吸烟者。这些结果表明,在没有明显动脉粥样硬化的个体中,ET -1对高血压病理生理学的影响比对其他危险因素的影响更大。