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首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Effect of metoprolol and verapamil administered separately and concurrently after single doses on liver blood flow and drug disposition.
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Effect of metoprolol and verapamil administered separately and concurrently after single doses on liver blood flow and drug disposition.

机译:单次给药后美托洛尔和维拉帕米分别或同时给药对肝血流量和药物处置的影响。

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摘要

Nine healthy males participated in a double-blind, placebo-controlled, randomized, crossover study to determine the effects of verapamil and metoprolol administered alone and concurrently on blood flow through the hepatic artery and portal and hepatic veins and to detect a possible drug interaction between the two agents. Single oral doses of placebo/placebo, metoprolol (50 mg)/placebo, verapamil (80 mg)/placebo, or verapamil/metoprolol were separated by at least 14 days. Liver blood flow through individual hepatic vessels was measured up to 8 hours after dosage administration using a duplex Doppler ultrasound technique. Cardiac output, heart rate, blood pressure, stroke volume, and total peripheral resistance were measured for 3 hours after drug doses were given. In 5 subjects, pharmacokinetic parameters for total drug as well as S- and R-enantiomers were also measured. Verapamil given alone caused a rapid and intense increase in liver blood flow (hepatic artery = 50%, portal vein = 42%, hepatic vein = 55%) 0.75 to 1 hour after administration because of a decrease in total peripheral resistance and an increase in heart rate, stroke volume, and cardiac output. Metoprolol given alone caused a slow but prolonged decrease in liver blood flow (maximum decrease: hepatic artery = -54%, portal vein = -21%, hepatic vein = -27%) 4 hours after administration because of a decrease in heart rate and cardiac output. When the two agents were given together, a composite of the changes noted after separate administration was noted: a brief peak increase in liver blood flow at 0.33 to 1 hour followed by a slow, prolonged decrease that reached its maximum decline 4 to 5 hours postdose. During the combined phase, metoprolol and its enantiomers had an increased AUC and Cmax, while verapamil and its enantiomers had an increased AUC and t1/2. These pharmacokinetic changes were consistent with the magnitude and time course of liver blood flow changes through the hepatic artery and portal or hepatic veins.
机译:九名健康男性参加了一项双盲,安慰剂对照,随机,交叉研究,以确定单独和同时施用维拉帕米和美托洛尔对通过肝动脉,门静脉和肝静脉的血流的影响,并检测两者之间可能存在的药物相互作用两位特工。单次口服剂量的安慰剂/安慰剂,美托洛尔(50 mg)/安慰剂,维拉帕米(80 mg)/安慰剂或维拉帕米/美托洛尔分开至少14天。使用双重多普勒超声技术在剂量给药后长达8小时测量通过单个肝血管的肝血流量。给予药物3个小时后,测量心输出量,心率,血压,中风量和总外周阻力。在5位受试者中,还测量了总药物以及S和R对映体的药代动力学参数。给药后0.75至1小时,单独服用维拉帕米会导致肝脏血流量迅速而强烈地增加(肝动脉= 50%,门静脉= 42%,肝静脉= 55%),因为总外周阻力降低且血脂增加。心率,中风量和心输出量。单独服用美托洛尔后,由于心率和心律的降低,导致肝血流量缓慢但长期下降(最大下降:肝动脉= -54%,门静脉= -21%,肝静脉= -27%)。心输出量。当将两种药物同时使用时,注意到单独给药后所注意到的变化的综合:在0.33至1小时内肝血流出现短暂的峰值增加,然后缓慢缓慢地下降,给药后4至5小时达到最大下降。在合并阶段,美托洛尔及其对映体的AUC和Cmax增加,而维拉帕米及其对映体的AUC和t1 / 2增加。这些药代动力学变化与通过肝动脉和门静脉或肝静脉的肝血流变化的幅度和时间进程一致。

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