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多巴酚丁胺在犬体内的处置。

Disposition of dobutamine in the dog.

作者信息

Murphy P J, Williams T L, Kau D L

出版信息

J Pharmacol Exp Ther. 1976 Nov;199(2):423-31.

PMID:978494
Abstract

The disposition of dobutamine, a potent inotropic catecholamine, has been examined in the dog. A sensitive assay has been developed for dobutamine allowing the measurement of the drug at plasma concentrations as low as 1 ng/ml. The short plasma half-life of dobutamine from the plasma to the tissue. When 14C-dobutamine was administered, the plasma half-life of radioactivity was 1.9 hours. The circulating radioactivity consists mainly of the glucuronide conjugate of 3-O-methyldobutamine. During continuous intravenous administration of dobutamine, plasma levels of metabolites reached a maximum between 3 and 4 hours. During a 48-hour time period after administration of 14C-dobutamine, 67% of the radiolable was excreted in the urine and 20% in the feces. In dogs having cannulated bile ducts, 30 to 35% of the administered drug was excreted in the bile. The major urinary metabolites were the glucuronide conjugates of dobutamine and 3-O-methyldobutamine.

摘要

已在犬类中研究了强效强心儿茶酚胺多巴酚丁胺的处置情况。已开发出一种灵敏的多巴酚丁胺测定法,可测量低至1纳克/毫升血浆浓度的该药物。多巴酚丁胺从血浆到组织的血浆半衰期较短。给予14C-多巴酚丁胺时,放射性的血浆半衰期为1.9小时。循环放射性主要由3-O-甲基多巴酚丁胺的葡萄糖醛酸共轭物组成。在持续静脉输注多巴酚丁胺期间,代谢物的血浆水平在3至4小时达到最高。给予14C-多巴酚丁胺后的48小时内,67%的放射性标记物经尿液排泄,20%经粪便排泄。在有胆管插管的犬类中,30%至35%的给药药物经胆汁排泄。主要的尿液代谢物是多巴酚丁胺和3-O-甲基多巴酚丁胺的葡萄糖醛酸共轭物。

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