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一系列剂量的阿替洛尔、索他洛尔和美托洛尔在48小时内对运动性心动过速的影响。

Effects on exercise tachycardia during forty-eight hours of a series of doses of atenolol, sotalol, and metoprolol.

作者信息

Harron D W, Balnave K, Kinney C D, Wilson R, Russell C J, Shanks R G

出版信息

Clin Pharmacol Ther. 1981 Mar;29(3):295-302. doi: 10.1038/clpt.1981.39.

Abstract

Beta adrenoceptor blockers differ mainly in their plasma elimination half-lives (t 1/2 s). It has been assumed that drugs with longer t 1/2 will have a longer duration of effect on exercise tachycardia. Several factors may influence the duration of action of beta blockers; we have investigated the contribution of plasma elimination t 1/2 and dose by comparing the effects on an exercise tachycardia in healthy subjects of placebo, 25, 50, 100, and 200 mg of atenolol and of sotalol, and 50, 100, 200, and 400 mg metoprolol. Subjects exercised before and at 2, 3, 6, 8, 24, 33, and 48 hr after oral doses of each drug. Plasma samples for measurement of drug concentration were drawn before each exercise period. Twenty-four hours after 50, 100, and 200 mg atenolol and 50, 100, 200, and 400 mg sotalol there were reductions in an exercise tachycardia; at this time reductions were greater after the larger doses. The plasma elimination t 1/2s of atenolol were between 7.2 +/0 1.0 hr. Although 50, 100, and 200 mg metoprolol induced the same reductions in an exercise tachycardia 2 hr after drug as 25, 50, and 100 mg atenolol and 50, 100, and 200 mg sotalol, these doses were without effect at 24 hr. Metoprolol 400 mg reduced exercise tachycardia at 24 hr but the effect was less than that of the three largest doses of atenolol and sotalol. The plasma elimination t 1/2 for metoprolol was between 3.6 +/- 0.6 and 5.0 +/- 1.8 hr. These results show that duration of cardiac beta blocking of cardiac beta blocking activity of atenolol, sotalol, and metoprolol is determined by the elimination t 1/2 and dose.

摘要

β肾上腺素受体阻滞剂的主要区别在于其血浆消除半衰期(t1/2)。人们认为,t1/2较长的药物对运动性心动过速的作用持续时间会更长。有几个因素可能会影响β受体阻滞剂的作用持续时间;我们通过比较安慰剂、25、50、100和200毫克阿替洛尔、索他洛尔以及50、100、200和400毫克美托洛尔对健康受试者运动性心动过速的影响,研究了血浆消除t1/2和剂量的作用。受试者在口服每种药物前以及服药后2、3、6、8、24、33和48小时进行运动。在每个运动阶段前采集血浆样本以测量药物浓度。服用50、100和200毫克阿替洛尔以及50、100、200和400毫克索他洛尔24小时后,运动性心动过速有所降低;此时,较大剂量后的降低幅度更大。阿替洛尔的血浆消除t1/2在7.2±1.0小时之间。虽然50、100和200毫克美托洛尔在服药后2小时对运动性心动过速的降低作用与25、50和100毫克阿替洛尔以及50、100和200毫克索他洛尔相同,但这些剂量在24小时时无效。400毫克美托洛尔在24小时时降低了运动性心动过速,但效果小于阿替洛尔和索他洛尔的三个最大剂量。美托洛尔的血浆消除t1/2在3.6±0.6至5.0±1.8小时之间。这些结果表明,阿替洛尔、索他洛尔和美托洛尔对心脏β受体阻滞活性的持续时间由消除t1/2和剂量决定。

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