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洋地黄毒苷在人体内的代谢及其受螺内酯的影响。

Metabolism of digitoxin in man and its modification by spironolactone.

作者信息

Wirth K E, Frölich J C, Hollifield J W, Falkner F C, Sweetman B S, Oates J A

出版信息

Eur J Clin Pharmacol. 1976 Mar 22;09(5-6):345-54. doi: 10.1007/BF00606547.

Abstract

The effect of spironolactone on the metabolism of intravenously administered 3H-digitoxin (80 muCi) was investigated in eight patients. In three of them the labelled glycoside was given on a second occasion after spironolactone treatment had been discontinued for at least 65 days. Of total urinary radioactivity 79% was unaltered drug and 12% consisted of water soluble compounds. No digitoxigenin or digoxigenin and only trace amounts (less than 2 %) of digoxin and the bis- and monoglycosides of digoxigenin were found. After spironolactone total urinary radioactivity was unchanged but the fraction eliminated as unchanged digitoxin fell from 79 to 66 % and the water soluble compounds increased from 12 to 26 % (p less than 0.05). In addition spironolactone caused a 20 ( reduction in the half-life of serum radioactivity (p less than 0.01) and a 16 % reduction in the volume of distribution (p less than 0.05). Induction of hepatic enzymes by spironolactone is proposed to explain the alteration in the metabolism of digitoxin in man. Both the altered metabolic pattern and the reduction in the volume of distribution appear to contribute to the reduction in half-life.

摘要

在8例患者中研究了螺内酯对静脉注射3H-洋地黄毒苷(80微居里)代谢的影响。其中3例患者在停用螺内酯治疗至少65天后再次给予标记糖苷。尿中总放射性的79%为未改变的药物,12%为由水溶性化合物组成。未发现洋地黄毒苷元或地高辛配基,仅发现痕量(小于2%)地高辛以及地高辛配基的双糖苷和单糖苷。使用螺内酯后,尿中总放射性未变,但以未改变的洋地黄毒苷形式消除的部分从79%降至66%,水溶性化合物从12%增至26%(p<0.05)。此外,螺内酯使血清放射性半衰期缩短20%(p<0.01),分布容积减少16%(p<0.05)。推测螺内酯诱导肝酶可解释其对人体洋地黄毒苷代谢的改变。代谢模式的改变和分布容积的减少似乎都导致了半衰期的缩短。

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