Okamoto Luis E, Gamboa Alfredo, Shibao Cyndya A, Arnold Amy C, Choi Leena, Black Bonnie K, Raj Satish R, Robertson David, Biaggioni Italo
From the Vanderbilt Autonomic Dysfunction Center and Division of Clinical Pharmacology, Department of Medicine (L.E.O., A.G., C.A.S., A.C.A., B.K.B., S.R.R., D.R., I.B.), and Departments of Pharmacology (S.R.R., D.R., I.B.), Neurology (D.R.), and Biostatistics (L.C.), Vanderbilt University School of Medicine, Nashville, TN.
Hypertension. 2014 Dec;64(6):1241-7. doi: 10.1161/HYPERTENSIONAHA.114.04116. Epub 2014 Sep 29.
Nebivolol, unlike other selective β1-receptor blockers, induces vasodilation attributable to increased NO bioavailability. The relative contribution of this mechanism to the blood pressure (BP)-lowering effects of nebivolol is unclear because it is normally masked by baroreflex buffering. Autonomic failure provides a unique model of hypertension devoid of autonomic modulation but sensitive to the hypotensive effects of NO potentiation. We tested the hypothesis that nebivolol would decrease BP in these patients through a mechanism independent of β-blockade. We randomized 20 autonomic failure patients with supine hypertension (14 men; 69±2 years) to receive a single oral dose of placebo, nebivolol 5 mg, metoprolol 50 mg (negative control), and sildenafil 25 mg (positive control) on separate nights in a double-blind, crossover study. Supine BP was monitored every 2 hours from 8:00 pm to 8:00 am. Compared with placebo, sildenafil and nebivolol decreased systolic BP during the night (P<0.001 and P=0.036, by mixed-effects model, maximal systolic BP reduction 8-hour postdrug of -20±6 and -24±9 mm Hg, respectively), whereas metoprolol had no effect. In a subanalysis, we divided patients into sildenafil responders (BP fall>20 mm Hg at 4:00 am) and nonresponders. Nebivolol significantly lowered systolic BP in sildenafil responders (-44±13 mm Hg) but not in nonresponders (1±11 mm Hg). Despite lowering nighttime BP, nebivolol did not worsen morning orthostatic tolerance compared with placebo. In conclusion, nebivolol effectively lowered supine hypertension in autonomic failure, independent of β1-blockade. These results are consistent with the hypothesis that NO potentiation contributes significantly to the antihypertensive effect of nebivolol.
奈必洛尔与其他选择性β1受体阻滞剂不同,它可通过增加一氧化氮(NO)生物利用度诱导血管舒张。该机制对奈必洛尔降压作用的相对贡献尚不清楚,因为它通常被压力反射缓冲所掩盖。自主神经功能衰竭提供了一种独特的高血压模型,该模型缺乏自主神经调节,但对NO增强的降压作用敏感。我们检验了以下假设:奈必洛尔可通过独立于β受体阻滞的机制降低这些患者的血压。在一项双盲交叉研究中,我们将20例患有仰卧位高血压的自主神经功能衰竭患者(14例男性;69±2岁)随机分组,让他们在不同夜晚分别单次口服安慰剂、5 mg奈必洛尔、50 mg美托洛尔(阴性对照)和25 mg西地那非(阳性对照)。从晚上8点到早上8点,每2小时监测一次仰卧位血压。与安慰剂相比,西地那非和奈必洛尔在夜间可降低收缩压(通过混合效应模型分析,P<0.001和P=0.036,给药后8小时收缩压最大降幅分别为-20±6和-24±9 mmHg),而美托洛尔无此作用。在一项亚分析中,我们将患者分为西地那非反应者(凌晨4点血压下降>20 mmHg)和无反应者。奈必洛尔可显著降低西地那非反应者的收缩压(-44±13 mmHg),但对无反应者无效(1±11 mmHg)。尽管奈必洛尔可降低夜间血压,但与安慰剂相比,它并未使早晨体位性耐受性恶化。总之,奈必洛尔可有效降低自主神经功能衰竭患者的仰卧位高血压,且独立于β1受体阻滞作用。这些结果与以下假设一致:NO增强对奈必洛尔的降压作用有显著贡献。