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木唑啉对肝源性腹水患者的药效学和药代动力学研究(作者译)

[Pharmacodynamic and pharmacokinetic studies of muzolimine in patients with hepatogeneous ascites (author's transl)].

作者信息

Loew D, Dýcka J, Pfleiderer T, Ritter W

出版信息

Z Gastroenterol. 1980 Oct;18(10):537-42.

PMID:7456563
Abstract

A clinical pharmacological study was carried out with 11 patients suffering from hepatogeneous ascites. After pretreatment with spironolactone (twice daily 100 mg), 80 mg of a new loop diuretic, muzolimine, were administered orally in addition to 100 mg of spironolactone. The diuretic effect started rapidly, reached its maximum about 6 h after administration and declined slowly until 24 h. The electrolyte profile showed a pronounced excretion of sodium and chloride, whereas potassium excretion was distinctly lower. Sodium/potassium ratio was 5.9 during the first 8 hours, and the mean ratio was 5.2 during 24 hours. Urinary volume and sodium excretion were significantly correlated with plasma levels of muzolimine. Mean plasma half-life of muzolimine in these patients with liver cirrhosis was 7.9 h and was thus longer than in healthy volunteers.

摘要

对11例肝源性腹水患者进行了临床药理学研究。在螺内酯预处理(每日2次,每次100mg)后,除给予100mg螺内酯外,口服80mg新型袢利尿剂莫唑胺。利尿作用起效迅速,给药后约6小时达到最大值,直至24小时缓慢下降。电解质分析显示钠和氯明显排泄增加,而钾排泄明显减少。最初8小时钠/钾比值为5.9,24小时平均比值为5.2。尿量和钠排泄与莫唑胺血浆水平显著相关。肝硬化患者中莫唑胺的平均血浆半衰期为7.9小时,因此比健康志愿者更长。

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