Pindolol: a pharmacokinetic comparison with other beta-adrenoceptor blocking agents.

J. Meier
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引用次数: 22

Abstract

SummaryThe pharmacokinetic properties of the 9 most frequently studied beta-adrenoceptor blocking agents (alprenolol, atenolol, metoprolol, oxprenolol, pindolol, practolol, propranolol, sotalol and timolol) are compared. Some pharmacokinetic parameters were found to be similar or not relevantly different in this group of drugs, e.g. the rate and amount of absorption, distribution volume, elimination half-life, total clearance and total urinary excretion. However, some other pharmacokinetic parameters, such as daily dosage, oral bioavailability, first-pass effect and the ratio of renal versus hepatic clearance, were surprisingly different. A good correlation between systemic availability and urinary excretion of unchanged drug could be demonstrated for the beta-adrenoceptor blocking agents.The pharmacokinetic comparison shows that pindolol has some relevant advantages. Due to the moderate metabolism, a negligible first-pass effect results which yields a high oral bioavailability and leads to small inter-in...
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品多洛尔:与其他β -肾上腺素受体阻滞剂的药代动力学比较。
摘要比较了常用的9种β -肾上腺素能受体阻滞剂(阿替诺尔、阿替洛尔、美托洛尔、奥异诺尔、品多洛尔、普萘洛尔、索他洛尔和替马洛尔)的药代动力学特性。该组药物的一些药代动力学参数相似或无相关差异,如吸收率和吸收量、分布体积、消除半衰期、总清除率和尿总排泄量。然而,其他一些药代动力学参数,如日剂量、口服生物利用度、首次通过效应和肾与肝清除率的比例,却惊人地不同。肾上腺素能受体阻滞剂的全身可用性与尿排泄之间存在良好的相关性。药代动力学比较表明品多洛尔具有一定的优势。由于代谢适中,可忽略不计的首过效应结果,产生高的口服生物利用度,导致小的内部…
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Investigations with beta-adrenoceptor blocking drugs in healthy volunteers. Pindolol: a pharmacokinetic comparison with other beta-adrenoceptor blocking agents. Lipoprotein lipase, hepatic lipase and plasma lipolytic activity. Effects of heparin and a low molecular weight heparin fragment (Fragmin). Studies on posthypoglycemic insulin resistance in insulin-dependent diabetes mellitus. Insulin resistance in Pima Indians. A combined effect of genetic predisposition and obesity-related skeletal muscle cell hypertrophy.
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