首页> 外文期刊>Pharmacology and Toxicology: An International Journal >Pharmacokinetics and antidiuretic effect of intravenous administration of desmopressin in orally overhydrated male volunteers.
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Pharmacokinetics and antidiuretic effect of intravenous administration of desmopressin in orally overhydrated male volunteers.

机译:在口服水合过度的男性志愿者中静脉注射去氨加压素的药代动力学和抗利尿作用。

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摘要

In order to study the antidiuretic activity of desmopressin in healthy human subjects, a study design has previously been used with subjects orally hydrated. The objective of the present study was to investigate the pharmacokinetics and the antidiuretic activity of desmopressin administered as an intravenous infusion to eight orally hydrated male volunteers. After initial ingestion of water corresponding to 15 ml.kg-1 body weight, the overhydration was maintained by replacing the urinary fluid loss by drinking-water. Desmopressin (4 micrograms) was administered intravenously over 10 min. 1.5 hr after the start of the hydration procedure. Blood was sampled and urine was collected at intervals throughout the study day (9.5 hr). The terminal half-life of elimination (t1/2,) of desmopressin was calculated to be 2.97 +/- 0.24 (S.E.M.) hr while the clearance was 1.77 +/- 0.10 ml.min.-1.kg-1 and the volume of distribution at steady state was 373 +/- 30 ml.kg-1. The infusion caused a marked and long-lasting reduction of the urine flow rate. Four hr after the start of the infusion the mean urine osmolality was 909 +/- 46 mOsm.kg-1.
机译:为了研究去氨加压素在健康人受试者中的抗利尿作用,先前已经对口服水合受试者使用了研究设计。本研究的目的是研究去氨加压素的静脉注射液对八名口服水合男性志愿者的药代动力学和抗利尿作用。最初摄入相当于15 ml.kg-1体重的水后,通过用饮用水代替尿液流失来维持水合过度。去氨加压素(4微克)经10分钟静脉内给药。水合程序开始后1.5小时。在整个研究日(9.5小时)中,定期取样并收集尿液。经计算,去氨加压素消除的最终半衰期(t1 / 2,)为2.97 +/- 0.24(SEM)小时,而清除率为1.77 +/- 0.10 ml.min.-1.kg-1稳态下的分布为373 +/- 30ml.kg-1。输注导致尿流率明显而持久的降低。输注开始后四小时,平均尿渗透压为909 +/- 46 mOsm.kg-1。

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