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健康成年人口服替唑米胺、呋塞米和安慰剂后利尿作用的数学模型。

Mathematical models of diuresis after oral administration of tizolemide, furosemide and placebo to healthy adults.

作者信息

Reyes A J, Leary W P, Venter C P

出版信息

J Int Med Res. 1981;9(1):18-20. doi: 10.1177/030006058100900104.

Abstract

Urine volumes and flows as functions of time after oral administration of placebo, furosemide 80 mg and tizolemide 100 mg to sixteen healthy male adults at 08.00 a.m. are described through mathematical models. Accumulated urine volumes after dosing, V, as functions of time, t, are accounted for by sigmoid functions and urine flows are described as dV/dt. No significant differences were found between the 24-hour urine volume mean values after furosemide (2457 ml) and tizolemide (2283 ml) and both were significantly higher than the corresponding mean value after placebo (1369 ml) ( p less than 0.001). Peak diuresis after dosing occurs about 1.5 hours for furosemide, 4 hours for tizolemide and 6 hours for placebo. Fourteen hours after dosing, urine volume amounts to 90% of the 24-hour urine volume after furosemide and to 76% after tizolemide, so that both substances may be regarded as diurnal diuretics.

摘要

通过数学模型描述了在上午8点给16名健康成年男性口服安慰剂、80毫克速尿和100毫克替唑米胺后,尿量和尿流随时间的变化情况。给药后累积尿量V作为时间t的函数,由S形函数表示,尿流描述为dV/dt。速尿(2457毫升)和替唑米胺(2283毫升)给药后24小时尿量平均值之间未发现显著差异,且两者均显著高于安慰剂给药后的相应平均值(1369毫升)(p<0.001)。给药后速尿的利尿峰值出现在约1.5小时,替唑米胺为4小时,安慰剂为6小时。给药后14小时,速尿给药后尿量达到24小时尿量的90%,替唑米胺给药后为76%,因此这两种物质均可视为日间利尿剂。

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