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阿替洛尔的降压作用时间进程:首次剂量与维持口服给药反应的比较。

Time-course of the anti-hypertensive action of atenolol: comparison of response to first dose and to maintained oral administration.

作者信息

Leonetti G, Terzoli L, Bianchini C, Sala C, Zanchetti A

出版信息

Eur J Clin Pharmacol. 1980 Nov;18(5):365-74. doi: 10.1007/BF00636787.

Abstract

To show whether repeated administration of atenolol for several days would influence its pharmacokinetic parameters and the extent and duration of the pharmacologic responses, the plasma level of atenolol and changes in heart rate, blood pressure and plasma renin activity were measured in 12 hypertensive patients at various times of day (9 a. m., 12 noon, 3 p. m. and 7 p. m.) after oral administration of the first dose of atenolol 100 mg, again during the 7th and 14th days of continued once-daily administration of the same dose, and finally during the three days following withdrawal of the drug. The peak plasma concentration of atenolol (about 600 ng/ml) was found 3 h after administration of the first dose, and measurable amounts (50-70 ng/ml) were found after 24 h. None of the pharmacokinetic characteristics were changed by administration of a single daily dose for two weeks. After withdrawal of the drug, detectable amounts of atenolol were found in plasma for at least 48 h. The first dose of atenolol caused prompt (3 h) and prolonged (up to 24 h) lowering of supine and standing systolic and diastolic blood pressures, slowing of supine and standing heart rate, reduction of the blood pressure and heart rate responses to dynamic exercise, and a decrease in plasma renin activity. The extent and time-course of all these responses were not influenced by repeated once-daily administration of the 100 mg dose for two weeks. Most of the effects continued during the withdrawal days, the lowering of blood pressure being somewhat more prolonged than the slowing of heart rate. It is concluded that a once-daily dose of atenolol 100 mg decreases blood pressure and heart rate throughout the following 24 h, without excessive daily fluctuation in its effects, and without signs of tolerance or accumulation.

摘要

为了探究连续数日服用阿替洛尔是否会影响其药代动力学参数以及药理反应的程度和持续时间,对12名高血压患者在口服首剂100毫克阿替洛尔后的不同时间点(上午9点、中午12点、下午3点和晚上7点)测量了阿替洛尔的血浆水平以及心率、血压和血浆肾素活性的变化。在连续每日服用相同剂量的第7天和第14天再次进行测量,最后在停药后的三天内进行测量。服用首剂后3小时发现阿替洛尔的血浆峰值浓度(约600纳克/毫升),24小时后仍可检测到一定量(50 - 70纳克/毫升)。连续两周每日单次给药并未改变任何药代动力学特征。停药后,血浆中至少48小时可检测到阿替洛尔。首剂阿替洛尔可迅速(3小时)并持续较长时间(长达24小时)降低仰卧位和站立位的收缩压和舒张压,减慢仰卧位和站立位心率,减弱对动态运动的血压和心率反应,并降低血浆肾素活性。连续两周每日单次服用100毫克剂量并未影响所有这些反应的程度和时间进程。大多数效应在停药期间仍持续存在,血压降低比心率减慢持续时间稍长。结论是,每日一次服用100毫克阿替洛尔可在接下来的24小时内降低血压和心率,其效应无过度的每日波动,也无耐受性或蓄积迹象。

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