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α-六氯环己烷的生物降解。IV. 体内单剂量的降解程度。

Biodegradation of alpha-hexachlorocyclohexane. IV. The extent of degradation of single doses in vivo.

作者信息

Noack G, Portig J, Wirsching M

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1975;288(1):57-64. doi: 10.1007/BF00501813.

Abstract
  1. Urine and stools were collected daily of 4 adult rats kept in single cages and injected once i.p. with alpha-hexachlorocyclohexane (alpha-HCH; dose per animal 126-150 mumoles), labelled uniformly with 14-C (10.8-14.0 X 10(6) dpm per animal). 2. In 4 weeks, 65% of the label was excreted through the kidneys and 16% by way of the intestine, with an estimated 8% being retained in depot fat. 3. GLC-analysis of the pooled urine showed it to contain very little unchanged drug, on average 0.05% of the dose. The time-course of the renal excretion of 14-C-labelled substance corresponded rather closely to the excretion of organically bound 36-Cl seen in earlier experiments with 36-Cl-labelled drug, indicating that the majority of urinary metabolites, presumably, still bear chlorine. 4. All or nearly all of the faecal 14-C was found by GLC to be accounted for by the stool's content of unchanged alpha-HCH. 5. Taken together, the results indicate a mean extent of alpha-HCH-degradation in the rat in the order of 80-85% of a dose. 6. Two rats were given 400 mg/kg of "cold" alpha-HCH by mouth 4 days before i.p. application of 14-C-labelled drug and were found to excrete more label through the kidneys in the first week than did the non-pretreated rats. This indicates that the drug stimulates its own degradation.
摘要
  1. 每天收集4只单笼饲养的成年大鼠的尿液和粪便,每只大鼠经腹腔注射一次α-六氯环己烷(α-HCH;每只动物剂量为126 - 150微摩尔),该物质用14-C均匀标记(每只动物10.8 - 14.0×10⁶ 每分钟衰变数)。

  2. 4周内,65%的标记物通过肾脏排出,16%通过肠道排出,估计8%保留在储存脂肪中。

  3. 对合并尿液的气相色谱分析表明,其中几乎不含未变化的药物,平均占剂量的0.05%。14-C标记物质的肾脏排泄时间进程与早期用36-Cl标记药物实验中观察到的有机结合36-Cl的排泄相当接近,这表明大部分尿液代谢物可能仍含有氯。

  4. 通过气相色谱法发现,粪便中的所有或几乎所有14-C都可由粪便中未变化的α-HCH含量解释。

  5. 综合来看,结果表明大鼠体内α-HCH的平均降解程度约为剂量的80 - 85%。

  6. 两只大鼠在腹腔注射14-C标记药物前4天经口给予400毫克/千克的“冷”α-HCH,发现它们在第一周通过肾脏排出的标记物比未预处理的大鼠更多。这表明该药物能刺激自身降解。

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