Diehl Kyle J, Stauffer Brian L, Dow Caitlin A, Bammert Tyler D, Brunjes Danielle L, Greiner Jared J, DeSouza Christopher A
From the Integrative Vascular Biology Laboratory, Department of Integrative Physiology, University of Colorado, Boulder (K.J.D., B.L.S., C.A.D., T.D.B., D.L.B., J.J.G., C.A.D.); Department of Medicine, University of Colorado, Denver (B.L.S., C.A.D.); and Department of Medicine, Denver Health Medical Center, CO (B.L.S.).
Hypertension. 2016 Jun;67(6):1196-204. doi: 10.1161/HYPERTENSIONAHA.115.06979. Epub 2016 Apr 25.
Endothelin-1 (ET-1) plays a major role in the pathophysiology of hypertension and its associated cardiovascular risk. We tested the hypothesis that chronic nebivolol treatment reduces ET-1-mediated vasoconstrictor tone in adult humans with elevated blood pressure (BP). Furthermore, reducing ET-1 vasoconstrictor activity contributes to the improvement in endothelial vasodilator function associated with nebivolol treatment. Forty-two middle-aged adults with elevated BP (systolic BP ≥130 mm Hg or diastolic BP ≥85 mm Hg) completed a 3-month, double-blind, randomized, placebo controlled trial: 14 received nebivolol (8 men/6 women; 5 mg per day); 14 received metoprolol succinate (9 men/5 women; 100 mg per day); and 14 received placebo (9 men/5 women). Forearm blood flow (plethysmography) responses to selective (BQ-123: 100 nmol/min; 60 minutes) and nonselective (BQ-123+BQ-788 [50 nmol/min]; 60 minutes) ET-1 receptor blockade, as well as acetylcholine (4.0, 8.0, and 16.0 μg per 100 mL of tissue per minute) in the absence and presence of nonselective ET-1 receptor blockade were determined before and after each treatment intervention. Forearm blood flow responses to BQ-123 and BQ-123+BQ-788 were similarly and significantly elevated (≈30% and 60%, respectively) from baseline in all 3 groups. Nebivolol, but not metoprolol or placebo, therapy resulted in a marked (≈25% and 45%; P<0.05) reduction in forearm blood flow response to BQ-123 and BQ-123+BQ-788. Moreover, after nebivolol therapy only, vasodilator response to acetylcholine was not significantly increased by ET-1 receptor blockade. These results demonstrate that nebivolol, but not metoprolol, treatment reduces ET-1-mediated vasoconstrictor tone in adult humans with elevated BP. In addition, nebivolol-induced reduction in ET-1-mediated vasoconstrictor tone underlies the favorable effects of this β-blocker on endothelial vasodilation.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT01395329.
内皮素 -1(ET -1)在高血压及其相关心血管风险的病理生理学中起主要作用。我们检验了以下假设:长期使用奈必洛尔治疗可降低血压升高的成年人中ET -1介导的血管收缩张力。此外,降低ET -1血管收缩活性有助于改善与奈必洛尔治疗相关的内皮血管舒张功能。42名血压升高的中年成年人(收缩压≥130mmHg或舒张压≥85mmHg)完成了一项为期3个月的双盲、随机、安慰剂对照试验:14人接受奈必洛尔治疗(8名男性/6名女性;每日5mg);14人接受琥珀酸美托洛尔治疗(9名男性/5名女性;每日100mg);14人接受安慰剂治疗(9名男性/5名女性)。在每次治疗干预前后,测定前臂血流量(体积描记法)对选择性(BQ -123:100nmol/min;60分钟)和非选择性(BQ -123 + BQ -788[50nmol/min];60分钟)ET -1受体阻断的反应,以及在不存在和存在非选择性ET -1受体阻断的情况下对乙酰胆碱(每分钟每100mL组织4.0、8.0和16.0μg)的反应。在所有3组中,对BQ -123和BQ -123 + BQ -788的前臂血流量反应与基线相比均有相似且显著的升高(分别约为30%和60%)。奈必洛尔治疗,但美托洛尔或安慰剂治疗未导致对BQ -123和BQ -123 + BQ -788的前臂血流量反应显著降低(约25%和约45%;P<0.05)。此外,仅在奈必洛尔治疗后,ET -1受体阻断未使对乙酰胆碱的血管舒张反应显著增加。这些结果表明,奈必洛尔治疗而非美托洛尔治疗可降低血压升高的成年人中ET -1介导的血管收缩张力。此外,奈必洛尔诱导的ET -1介导的血管收缩张力降低是该β受体阻滞剂对内皮血管舒张产生有利作用的基础。