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地高辛还原代谢产物的尿排泄

Urinary excretion of reduced metabolites of digoxin.

作者信息

Lindenbaum J, Tse-Eng D, Butler V P, Rund D G

出版信息

Am J Med. 1981 Jul;71(1):67-74. doi: 10.1016/0002-9343(81)90260-6.

Abstract

The urinary excretion of the relatively cardioinactive reduced metabolites of digoxin, dihydrodigoxin and related compounds was measured by radioimmunoassay in 131 normal subjects during studies of the bioavailability of digoxin preparations. Digoxin reduction products (DRP) constitute more than 5 percent of the excretion of digoxin and its metabolites in one-third of the volunteers after the administration of single or multiple doses of digoxin. There was little or no output of DRP during the first 8 hours after a single dose, with maximal excretion usually occurring on the second day. Most subjects who excreted more than 5 percent DRP on one occasion did so with each subsequent exposure to digoxin. Six volunteers, however, in whom substantial amounts of DRP had previously been found, failed to excrete detectable quantities after subsequent doses. In two, this change occurred shortly after they took erythromycin. Urinary DRP were less after the intravenous administration compared to the oral administration of digoxin. After oral doses, DRP excretion tended to vary inversely with the bioavailability of the preparation. The findings are consistent with the hypothesis that DRP are formed as the result of the activity of a variable component of the intestinal flora. Prospective studies will be necessary to prove this hypothesis.

摘要

在一项地高辛制剂生物利用度研究中,采用放射免疫分析法对131名正常受试者地高辛、二氢地高辛及相关化合物相对心脏活性较低的还原代谢产物的尿排泄情况进行了测定。在单次或多次服用地高辛后,三分之一的志愿者体内,地高辛还原产物(DRP)占地高辛及其代谢产物排泄量的5%以上。单次给药后的前8小时,DRP排出量很少或没有,最大排泄量通常出现在第二天。大多数一次排泄DRP超过5%的受试者,在随后每次服用地高辛时均如此。然而,此前发现有大量DRP的6名志愿者,在后续给药后未能排出可检测量的DRP。其中两名志愿者在服用红霉素后不久就出现了这种变化。与口服地高辛相比,静脉注射后尿中DRP较少。口服给药后,DRP排泄量往往与制剂的生物利用度呈负相关。这些发现与以下假设一致,即DRP是肠道菌群可变成分活性的结果。需要进行前瞻性研究来证实这一假设。

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