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布美他尼与呋塞米的相互作用研究。丙磺舒和吲哚美辛对人体布美他尼反应的影响。

Interaction studies with bumetanide and furosemide. Effects of probenecid and of indomethacin on response to bumetanide in man.

作者信息

Brater D C, Fox W R, Chennavasin P

出版信息

J Clin Pharmacol. 1981 Nov-Dec;21(11):647-53. doi: 10.1002/j.1552-4604.1981.tb05677.x.

Abstract

Bumetanide was administered intravenously in doses of 0.5 and 1.0 mg to eight normal subjects with and without pretreatment with probenecid or indomethacin. Probenecid did not affect either the cumulative response or the time course of response to bumetanide. This may mean that probenecid and potentially other exogenous or endogenous organic acids do not affect the renal handling of bumetanide in normal man. Indomethacin pretreatment decreased the cumulative 4-hour excretion of sodium caused by 1.0 mg bumetanide from 276 +/- 22.9 to 202 +/- 20.9 mEq (P less than 0.003). Effects on volume and chloride paralleled those of sodium, while potassium excretion was not affected. When the response was analyzed as increment in fractional excretion over basal solute excretion, determined from separate control studies, indomethacin still decreased the response, possibly indicating that endogenous prostaglandins may play a role in determining the overall response to bumetanide.

摘要

对8名正常受试者静脉注射0.5毫克和1.0毫克剂量的布美他尼,部分受试者预先使用丙磺舒或吲哚美辛进行预处理。丙磺舒对布美他尼的累积反应或反应的时间进程均无影响。这可能意味着丙磺舒以及其他潜在的外源性或内源性有机酸不会影响正常人体内布美他尼的肾脏处理过程。预先使用吲哚美辛进行预处理,使1.0毫克布美他尼导致的4小时钠累积排泄量从276±22.9毫当量降至202±20.9毫当量(P<0.003)。对血容量和氯离子的影响与对钠的影响相似,而钾排泄不受影响。当将反应分析为相对于基础溶质排泄的分数排泄增量时(根据单独的对照研究确定),吲哚美辛仍然会降低反应,这可能表明内源性前列腺素可能在决定对布美他尼的总体反应中发挥作用。

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