Masumoto A, Hirooka Y, Shimokawa H, Hironaga K, Setoguchi S, Takeshita A
Department of Cardiovascular Medicine, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
Hypertension. 2001 Dec 1;38(6):1307-10. doi: 10.1161/hy1201.096541.
Rho-kinase plays an important role in modulating Ca(2+) sensitivity of vascular smooth muscle and has been suggested to be involved in the increased systemic vascular resistance in hypertensive animals. However, it remains to be examined whether this is also the case in patients with essential hypertension. Recently, it has been shown that fasudil is a specific Rho-kinase inhibitor. The aim of this study was to examine whether Rho-kinase is involved in the pathogenesis of hypertension in humans by using this Rho-kinase inhibitor. Studies were performed in hypertensive patients (HT group, n=14) and age-matched normotensive subjects (NT group, n=12). Forearm blood flow was measured by a strain-gauge plethysmograph during intra-arterial infusion of graded doses of fasudil (3.2, 6.4, 12.8, and 25.6 microg/min) or sodium nitroprusside (0.4, 0.8, 1.6, and 3.2 microg/min). Resting forearm vascular resistance was significantly higher in the HT group than in the NT group (22+/-4 versus 17+/-5 U, respectively; P<0.05). The extent of the increase in forearm blood flow evoked by fasudil was significantly greater in the HT group than in the NT group (12.3+/-1.4 versus 6.0+/-0.6 mL. min(-1). 100 mL(-1), respectively; P<0.01). The percent decrease in forearm vascular resistance was significantly greater in the HT group than in the NT group (63.6+/-4.7% versus 29.6+/-3.9%, respectively; P<0.01). By contrast, forearm vasodilator response evoked by sodium nitroprusside was comparable between the 2 groups. These results provide the first evidence that Rho-kinase may be involved in the pathogenesis of the increased peripheral vascular resistance in hypertension in humans.
Rho激酶在调节血管平滑肌的钙敏感性方面发挥着重要作用,并且有人认为它与高血压动物全身血管阻力增加有关。然而,原发性高血压患者是否也是如此仍有待研究。最近,已证明法舒地尔是一种特异性Rho激酶抑制剂。本研究的目的是通过使用这种Rho激酶抑制剂来研究Rho激酶是否参与人类高血压的发病机制。对高血压患者(HT组,n = 14)和年龄匹配的血压正常受试者(NT组,n = 12)进行了研究。在动脉内输注不同剂量的法舒地尔(3.2、6.4、12.8和25.6微克/分钟)或硝普钠(0.4、0.8、1.6和3.2微克/分钟)期间,用应变片体积描记器测量前臂血流量。HT组静息前臂血管阻力显著高于NT组(分别为22±4与17±5 U;P<0.05)。法舒地尔引起的前臂血流量增加幅度在HT组显著大于NT组(分别为12.3±1.4与6.0±0.6毫升·分钟-1·100毫升-1;P<0.01)。HT组前臂血管阻力降低的百分比显著大于NT组(分别为63.6±4.7%与29.6±3.9%;P<0.01)。相比之下,硝普钠引起的前臂血管舒张反应在两组之间相当。这些结果提供了首个证据,表明Rho激酶可能参与人类高血压中外周血管阻力增加的发病机制。