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磺胺甲恶唑在人体内会代谢为羟胺。

Sulfamethoxazole is metabolized to the hydroxylamine in humans.

作者信息

Cribb A E, Spielberg S P

机构信息

Department of Paediatrics, University of Toronto, Ontario, Canada.

出版信息

Clin Pharmacol Ther. 1992 May;51(5):522-6. doi: 10.1038/clpt.1992.57.

Abstract

The oxidation of sulfamethoxazole to its hydroxylamine metabolite was investigated in vitro with human liver microsomes and in vivo by detection in the urine. Sulfamethoxazole was oxidized to the hydroxylamine in an NADPH-dependent process by liver microsomes prepared from two human livers. Three healthy volunteers ingested 1000 mg sulfamethoxazole, and urine was collected for 24 hours. Sulfamethoxazole hydroxylamine constituted 3.1% +/- 0.7% of the drug excreted in the urine in 24 hours. Fifty-four percent of the ingested dose was excreted during this same time period. We conclude that sulfamethoxazole hydroxylamine is an authentic in vivo metabolite in humans, probably formed predominantly by cytochrome P450 in the liver. It could be responsible for mediation of sulfonamide adverse reactions, particularly hypersensitivity reactions.

摘要

利用人肝微粒体在体外研究了磺胺甲恶唑氧化为其羟胺代谢物的过程,并通过检测尿液在体内进行了研究。由两颗人肝脏制备的肝微粒体通过依赖于NADPH的过程将磺胺甲恶唑氧化为羟胺。三名健康志愿者服用了1000毫克磺胺甲恶唑,并收集尿液24小时。磺胺甲恶唑羟胺占24小时尿液中排泄药物的3.1%±0.7%。在同一时间段内,摄入剂量的54%被排泄。我们得出结论,磺胺甲恶唑羟胺是人类体内一种真实的代谢物,可能主要由肝脏中的细胞色素P450形成。它可能是磺胺类药物不良反应,特别是过敏反应的介导因素。

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