Hryniewicz Katarzyna, Androne Ana Silvia, Hudaihed Alhakam, Katz Stuart D
Department of Medicine, Columbia University College of Physicians & Surgeons, New York, NY, USA.
Circulation. 2003 Aug 26;108(8):971-6. doi: 10.1161/01.CIR.0000085070.39873.B1. Epub 2003 Aug 11.
Adrenergic receptor blockers used in the treatment of heart failure have distinct receptor affinity profiles. We hypothesized that alpha-adrenergic-blocking effects of carvedilol would limit vasoconstriction in response to adrenergic stimuli when compared with metoprolol.
Forearm vascular resistance responses to isometric handgrip and cold pressor test were determined by plethysmography before and during adrenergic receptor blockade in prospective randomized trials. Acute effects were assessed in a crossover trial in normal subjects (single dose of 25 mg carvedilol, 100 mg metoprolol tartrate, and placebo). Chronic effects (25 mg carvedilol BID versus 200 mg extended-release metoprolol succinate daily for 6 months) were assessed in a parallel group trial of chronic heart failure subjects. In normal subjects, carvedilol decreased forearm vascular resistance responses to adrenergic stimuli when compared with metoprolol and placebo (isometric handgrip -3.5 U for carvedilol versus -1.2 U for metoprolol and -2.2 U for placebo, P=0.15; cold pressor test 3.1+/-8.9 U for carvedilol versus 9.0+/-2.7 U for metoprolol and 8.2+/-5.8 U for placebo, P<0.05). In heart failure subjects, vasomotor responses to isometric handgrip and cold pressor test did not differ between treatment groups.
Acute administration of carvedilol attenuates the vasoconstriction response to adrenergic stimuli when compared with placebo and metoprolol in normal subjects, whereas chronic administration of carvedilol does not attenuate the vasoconstrictor response to adrenergic stimuli when compared with metoprolol in heart failure subjects. These data suggest that long-term benefits of carvedilol in heart failure are not mediated by alpha-adrenergic blockade.
用于治疗心力衰竭的肾上腺素能受体阻滞剂具有不同的受体亲和力特征。我们推测,与美托洛尔相比,卡维地洛的α-肾上腺素能阻滞作用会限制对肾上腺素能刺激的血管收缩反应。
在前瞻性随机试验中,通过体积描记法在肾上腺素能受体阻滞前后测定前臂血管阻力对等长握力和冷加压试验的反应。在正常受试者的交叉试验中评估急性效应(单剂量25 mg卡维地洛、100 mg酒石酸美托洛尔和安慰剂)。在慢性心力衰竭受试者的平行组试验中评估慢性效应(卡维地洛25 mg每日两次与琥珀酸美托洛尔缓释片200 mg每日一次,共6个月)。在正常受试者中,与美托洛尔和安慰剂相比,卡维地洛降低了前臂血管阻力对肾上腺素能刺激的反应(等长握力:卡维地洛为-3.5 U,美托洛尔为-1.2 U,安慰剂为-2.2 U,P = 0.15;冷加压试验:卡维地洛为3.1±8.9 U,美托洛尔为9.0±2.7 U,安慰剂为8.2±5.8 U,P<0.05)。在心力衰竭受试者中,各治疗组对等长握力和冷加压试验的血管舒缩反应无差异。
与安慰剂和美托洛尔相比,在正常受试者中急性给予卡维地洛可减弱对肾上腺素能刺激的血管收缩反应,而在心力衰竭受试者中,与美托洛尔相比,慢性给予卡维地洛不会减弱对肾上腺素能刺激的血管收缩反应。这些数据表明,卡维地洛在心力衰竭中的长期益处并非由α-肾上腺素能阻滞介导。