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稳定前列环素类似物ZK 36 374在猫体内的药代动力学和药效学

Pharmacokinetics and pharmacodynamics of the stable prostacyclin analogue, ZK 36 374, in the cat.

作者信息

Krause W, Beckmann R, Schubert M

出版信息

Prostaglandins Leukot Med. 1984 Aug;15(2):187-97. doi: 10.1016/0262-1746(84)90176-8.

Abstract

The pharmacokinetics and the pharmacologic effect on blood pressure and heart rate of ZK 36 374 were studied simultaneously in the unanaesthetized cat following intraarterial injection of 20 micrograms/kg of tritium-labelled drug. After a rapid distribution phase the plasma level of radioactive substances declined with a half-life of 44 min. The disposition of the unchanged drug was biphasic with half-lives of 7 min and 36 min. 1.5 min after injection, the systolic and diastolic blood pressures were depressed by 40 and 57% and the heart rate rose by 18%. The kinetics of the pharmacologic action was biphasic and strictly parallel to the plasma drug level. Accordingly, there was a highly significant (p less than 0.001) logarithmic correlation between the blood pressure depression and the concentration of unchanged ZK 36 374 in the plasma. ZK 36 374 was totally metabolized and excreted nearly equally with urine and feces in the form of more than eight metabolites.

摘要

在未麻醉的猫身上,通过动脉内注射20微克/千克的氚标记药物ZK 36 374,同时研究了其药代动力学以及对血压和心率的药理作用。在快速分布相之后,放射性物质的血浆水平以44分钟的半衰期下降。原形药物的处置呈双相,半衰期分别为7分钟和36分钟。注射后1.5分钟,收缩压和舒张压分别下降40%和57%,心率上升18%。药理作用的动力学呈双相,且与血浆药物水平严格平行。因此,血压降低与血浆中未代谢的ZK 36 374浓度之间存在高度显著(p小于0.001)的对数相关性。ZK 36 374完全代谢,以超过八种代谢物的形式通过尿液和粪便几乎等量排泄。

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