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去甲麻黄碱在人、兔和大鼠体内代谢的种属差异。

Species differences in the metabolism of norephedrine in man, rabbit and rat.

作者信息

Sinsheimer J E, Dring L G, Williams R T

出版信息

Biochem J. 1973 Nov;136(3):763-71. doi: 10.1042/bj1360763.

Abstract
  1. (+/-)-2-Amino-1-phenyl[1-(14)C]propan-1-ol ([(14)C]norephedrine) was administered orally to man, rat and rabbit and the metabolites excreted in the urine were identified and measured. Pronounced species differences in the metabolism of the drug were found. 2. Three male human subjects, receiving 25mg each of [(14)C]norephedrine hydrochloride, excreted over 90% of the (14)C in the first day. The main metabolite was the unchanged drug (86% of the dose) and minor metabolites were hippuric acid and 4-hydroxynorephedrine. 3. In rats given 12mg of the drug/kg almost 80% of the (14)C administered was excreted in the first day. The major metabolites in the urine were the unchanged drug (48% of the dose), 4-hydroxynorephedrine (28%) and trace amounts of side-chain degradation products. 4. Rabbits given 12mg of the drug/kg excreted 85-95% of the dose of (14)C in the urine in the first 24h after dosing. The major metabolites in the urine were conjugates of 1,2-dihydroxy-1-phenylpropane (31% of the dose) and of 1-hydroxy-1-phenylpropan-2-one (27%) and hippuric acid (20%). The unchanged drug was excreted in relatively small amounts (8%).
摘要
  1. 给人、大鼠和兔子口服(±)-2-氨基-1-苯基[1-(14)C]丙-1-醇([(14)C]去甲麻黄碱),并对尿液中排泄的代谢产物进行鉴定和测量。发现该药物的代谢存在明显的种属差异。2. 三名男性受试者每人服用25毫克[(14)C]盐酸去甲麻黄碱,第一天排泄出超过90%的(14)C。主要代谢产物是未变化的药物(占剂量的86%),次要代谢产物是马尿酸和4-羟基去甲麻黄碱。3. 给大鼠按每千克体重12毫克的剂量给药,给药后第一天排泄出近80%的(14)C。尿液中的主要代谢产物是未变化的药物(占剂量的48%)、4-羟基去甲麻黄碱(28%)和微量的侧链降解产物。4. 给兔子按每千克体重12毫克的剂量给药,给药后24小时内,尿液中排泄出85 - 95%的(14)C剂量。尿液中的主要代谢产物是1,2-二羟基-1-苯基丙烷的结合物(占剂量的31%)、1-羟基-1-苯基丙-2-酮的结合物(27%)和马尿酸(20%)。未变化的药物排泄量相对较少(8%)。

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[Metabolism and tissular distribution of d1-ephedrine 14C].[14C标记的d1-麻黄碱的代谢与组织分布]
Biochem Pharmacol. 1968 Nov;17(11):2319-31. doi: 10.1016/0006-2952(68)90040-3.
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