Department of Medicine, Division of Clinical Pharmacology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Pharmacogenet Genomics. 2013 Jan;23(1):25-8. doi: 10.1097/FPC.0b013e32835afde6.
The β1-adrenergic receptor (β1AR) Arg389Gly polymorphism affects responses to orally administered β1AR antagonists (β-blockers) in vivo. However, the effect of this polymorphism on the early heart rate response to β-blockers has not been evaluated. The aim of this study was to determine the effect of the Arg389Gly polymorphism on the inhibition of exercise-induced tachycardia by esmolol, an ultra-short-acting intravenously administered β1AR antagonist. Healthy nonsmoking White individuals were enrolled on the basis of their ADRB1 genotype, including carriers of 0, 1 or 2 Arg389 alleles (n=9 in each group, total 27, 18 men). Placebo and esmolol were infused consecutively for 10 min each, separated by 30 min. At the end of each infusion, participants performed dynamic handgrip exercise. Heart rate and blood pressure were compared among three ADRB1 genotypes. Carriers of 0, 1, or 2 Arg389 alleles varied significantly in both exercise-induced tachycardia during esmolol (P(ANOVA)=0.030) and esmolol inhibition of exercise-induced tachycardia [0.78±7.70, 5.11±4.05, 10.22±9.78 bpm, respectively (P=0.014)]. The early effect of esmolol on exercise-induced tachycardia was significantly greater among Arg389 than in Gly389 homozygote healthy individuals (NCT01388036).
β1-肾上腺素能受体(β1AR)Arg389Gly 多态性影响体内口服β1AR 拮抗剂(β 阻断剂)的反应。然而,这种多态性对β阻断剂引起的早期心率反应的影响尚未得到评估。本研究旨在确定 Arg389Gly 多态性对依托咪酯(一种超短效静脉内给予的β1AR 拮抗剂)抑制运动引起的心动过速的影响。根据 ADRB1 基因型,包括携带 0、1 或 2 个 Arg389 等位基因的健康非吸烟白种人(每组 9 人,共 27 人,18 名男性)入选。连续输注安慰剂和依托咪酯各 10 分钟,间隔 30 分钟。在每次输注结束时,参与者进行动态握力运动。比较三种 ADRB1 基因型之间的心率和血压。携带 0、1 或 2 个 Arg389 等位基因的个体在依托咪酯引起的运动性心动过速(P(ANOVA)=0.030)和依托咪酯抑制运动性心动过速方面存在显著差异[0.78±7.70、5.11±4.05、10.22±9.78 bpm,分别(P=0.014)]。与 Gly389 纯合子健康个体相比,Arg389 个体中依托咪酯对运动性心动过速的早期作用明显更大(NCT01388036)。