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依他唑啉/奥唑啉酮在肾功能正常和受损的高血压患者中的药效学和药代动力学。

Pharmacodynamics and kinetics of etozolin/ozolinone in hypertensive patients with normal and impaired kidney function.

作者信息

Knauf H, Liebig R, Schollmeyer P, Rosenthal J, Kölle E U, Mutschler E

出版信息

Eur J Clin Pharmacol. 1984;26(6):687-93. doi: 10.1007/BF00541926.

DOI:10.1007/BF00541926
PMID:6386484
Abstract

The effect on urinary electrolyte excretion, renin release and plasma norepinephrine of single oral doses of 400 mg etozolin (E) and of 40 mg furosemide (F) were studied in hypertensive patients with normal (n = 6) and impaired kidney function (n = 6). E caused a marked saluresis up to 24 hours, showing its long duration of action. F, however, displayed a brief, brisk peak diuresis, followed by a rebound from the 4th to the 24th hours. The brisk peak diuresis induced by F was associated with pronounced release of renin, almost twice that induced by E. In chronic renal failure the renin release in relation to the magnitude of the diuresis was increased, i.e. the sensitivity of these patients to changes in water homeostasis was increased. E and F stimulated the sympathetic system to roughly the same extent. Patients with essential hypertension had higher plasma levels of norepinephrine than hypertensive patients with chronic renal failure. In addition, hypertensive patients with normal renal function (n = 4) and varying degrees of renal impairment (n = 11) were also given 400 mg daily for 2 weeks. Effects on blood pressure and electrolyte homeostasis were monitored, as well as the plasma kinetics of metabolite I, ozolinone. At the end of the 2 week treatment E had significantly lowered systolic (-12 mm Hg) and diastolic (-9 mm Hg) blood pressure, and had produced a significant loss of body weight, without altering plasma electrolytes or blood chemistry. There was no accumulation of the effective metabolite ozolinone under conditions of severe impairment of kidney function.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在肾功能正常(n = 6)和肾功能受损(n = 6)的高血压患者中,研究了单次口服400 mg依托唑啉(E)和40 mg呋塞米(F)对尿电解质排泄、肾素释放和血浆去甲肾上腺素的影响。E可引起长达24小时的显著利钠作用,显示其作用持续时间长。然而,F表现出短暂、迅速的利尿高峰,随后在第4至24小时出现反跳。F诱导的迅速利尿高峰与肾素的显著释放有关,几乎是E诱导释放量的两倍。在慢性肾衰竭中,与利尿幅度相关的肾素释放增加,即这些患者对水平衡变化的敏感性增加。E和F对交感神经系统的刺激程度大致相同。原发性高血压患者的血浆去甲肾上腺素水平高于慢性肾衰竭高血压患者。此外,肾功能正常(n = 4)和不同程度肾功能损害(n = 11)的高血压患者也每日服用400 mg,持续2周。监测对血压和电解质稳态的影响以及代谢物I(奥唑啉酮)的血浆动力学。在2周治疗结束时,E显著降低了收缩压(-12 mmHg)和舒张压(-9 mmHg),并导致体重显著减轻,而未改变血浆电解质或血液化学指标。在肾功能严重受损的情况下,有效代谢物奥唑啉酮没有蓄积。(摘要截短于250字)

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