Sund R B
Department of Pharmacology, University of Oslo, Blindern, Norway.
Pharmacol Toxicol. 1987 Aug;61(2):130-7. doi: 10.1111/j.1600-0773.1987.tb01790.x.
Rats were infused with danthron (I) at doses of 0.48, 2.2 and 5.8 mumol/100 g body weight, or given 12 mumol/100 g with gastric tube. TLC of bile and urine demonstrated a number of metabolites, at both administration routes. These included I monosulphate (II) and -glucuronide (III), two other phase 2 metabolites which behaved as the corresponding diconjugates, and several phase 1 metabolites (IV) in conjugated form. IV as a group were estimated by photometry of hydrolysed samples, using I as a reference. Danthron conjugates as a group were determined in such samples by a specific method for I. Moreover, II and III were determined individually in unhydrolysed specimens. Following infusion, about 80% of the danthron conjugates in bile were excreted after 1 hour; the dose fractions found after 5 hours represented about 20%, 30%, and 40% at the low, intermediate and high dose level, respectively. The corresponding fractions in urine were 16%, 12% and 10%, giving rise to bile:urine excretion ratios of 1.3, 2.7 and 4.0, respectively. This change in excretion pattern was associated with changes in metabolite muster, which involved a decrease in the balance of IV:I conjugates, as well as an increase in III:II ratio. IV was more abundantly present in bile than in urine, and showed a more sustained excretion than the I conjugates. By intragastric administration, the cumulated excretion (bile + urine) of I conjugates were only 6%, 8% and 5% of dose, in three consecutive 6 hours' periods (0-6, 6-12 and 12-18 hours after dosing). The bile:urine excretion ratios seemed to decrease with time, as did the III:II ratio.(ABSTRACT TRUNCATED AT 250 WORDS)
给大鼠分别按0.48、2.2和5.8微摩尔/100克体重的剂量注入丹蒽醌(I),或通过胃管给予12微摩尔/100克。胆汁和尿液的薄层色谱法显示,两种给药途径均产生了多种代谢物。这些代谢物包括I的单硫酸盐(II)和葡萄糖醛酸苷(III),另外两种II相代谢物表现为相应的双共轭物,以及几种呈共轭形式的I相代谢物(IV)。以I为参比,通过水解样品的光度法对IV组进行估算。通过一种针对I的特定方法测定此类样品中的丹蒽醌共轭物组。此外,在未水解的标本中分别测定II和III。注入后,胆汁中约80%的丹蒽醌共轭物在1小时后排出;在低、中、高剂量水平下,5小时后发现的剂量分数分别约为20%、30%和40%。尿液中的相应分数分别为16%、12%和10%,胆汁与尿液的排泄比分别为1.3、2.7和4.0。排泄模式的这种变化与代谢物组成的变化相关,这涉及IV:I共轭物平衡的降低以及III:II比率的增加。IV在胆汁中的含量比在尿液中更丰富,并且排泄比I共轭物更持久。通过胃内给药,在连续三个6小时时间段(给药后0 - 6、6 - 12和12 - 18小时)内,I共轭物的累积排泄量(胆汁 + 尿液)仅为剂量的6%、8%和5%。胆汁与尿液的排泄比似乎随时间降低,III:II比率也是如此。(摘要截断于250字)