Glybuzole(2-Benzenesulfonamido-5-tert-butyl-1-thia-3,4-diazole)のフエノバルビタール, SKF 525Aおよび四塩化炭素前処理ラットにおける代謝

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タイトル別名
  • Metabolism of Glybuzole (2-Benzenesulfonamido-5-tert-butyl-1-thia-3, 4-diazole) in Rats after Pretreatment of Phenobarbital, SKF 525A and Carbon Tetrachloride
  • Glybuzole 2 Benzenesulfonamido 5 tert b

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Absorption, excretion, and metabolism of Glybuzole (2-benzenesulfonamido-5-tert-butyl-1-thia-3, 4-diazole) were studied in normal rats, and rats pretreated with phenobarbital, SKF 525A, or carbon tetrachloride. Plasma half-life of 14C-Glybuzole after its oral administration was affected by the pretreatment ; phenobarbital, 4.5 hr ; SKF 525A, 28 hr ; carbon tetrachloride, 34 hr ; and nontreated, 7 hr. Urinary, fecal, and biliary excretion of Glybuzole was also affected by these pretreatments. Glybuzole was excreted in urine 2.5 times higher in carbon tetrachloride-pretreated rats than in normal rats. Biliary excretion of Glybuzole in normal rats reached 91.1% of administered radioactivity within 48 hr, indicating the presence of enterohepatic circulation. Major urinary metabolites were the unchanged drug, a metabolite (I) oxidized at the tert-butyl side-chain, a novel metabolite (II) oxidized at the position para to the phenyl group of Glybuzole, and their O- or N-glucuronides. Unchanged drug was major and metabolites I and II were minor components. In bile, glucuronides, mainly N-glucuronide of Glybuzole, were major metabolites. Carbon tetrachloride pretreatment suppressed the excretion of N-glucuronide. The plasma metabolites (I and II) had no antidiabetic activity in rabbits.

収録刊行物

  • 薬学雑誌

    薬学雑誌 98 (9), 1208-1214, 1978

    公益社団法人 日本薬学会

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