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D-青霉胺在DA品系大鼠体内的代谢与处置

The metabolism and disposition of D-penicillamine in the DA-strain rat.

作者信息

Pilkington A E, Waring R H

机构信息

Department of Biochemistry, University of Birmingham, UK.

出版信息

Eur J Drug Metab Pharmacokinet. 1988 Apr-Jun;13(2):99-104. doi: 10.1007/BF03191310.

Abstract

Radiolabelled [35S]-D-penicillamine was administered orally to DA-strain rats. After 72 hours approximately 65% of the dose was excreted with no significant differences between male and female animals. The major urinary product was inorganic sulphate with small amounts of D-penicillamine. Penicillamine disulphide, penicillamine-cysteine, S-methyl penicillamine and N-acetyl penicillamine were also found as metabolites. The female rat excreted significantly less sulphate (P less than 0.1) and more penicillamine disulphide (P less than 0.01) than the male. The residual radioactivity was found in the carcass, with slight concentration in the gut, skin, kidney, bladder and liver.

摘要

给DA品系大鼠口服放射性标记的[35S]-D-青霉胺。72小时后,约65%的剂量被排泄,雄性和雌性动物之间无显著差异。主要的尿液产物是无机硫酸盐,还有少量的D-青霉胺。还发现青霉胺二硫化物、青霉胺-半胱氨酸、S-甲基青霉胺和N-乙酰青霉胺为代谢产物。雌性大鼠排泄的硫酸盐显著少于雄性大鼠(P<0.1),而排泄的青霉胺二硫化物则显著多于雄性大鼠(P<0.01)。在 carcass 中发现了残留放射性,在肠道、皮肤、肾脏、膀胱和肝脏中有轻微富集。 (注:carcass 此处翻译存疑,因未明确其在原文语境中的准确含义,暂保留英文,可能是“尸体”“动物躯体”等意思 )

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