Phillips R D, Berndt W O, Hayes A W
Toxicology. 1979 Mar-Apr;12(3):285-98. doi: 10.1016/0300-483x(79)90075-1.
The distribution and excretion of radioactivity from [14C]citrinin (3 mg/kg, i.v) was determined in male rats. At 0.5 h after administration maximum values of 14.7% and 5.6% of total radioactivity were observed in the liver and kidneys, respectively, and by 6 h decreased to 7.5% in the liver and 4.7% in the kidney. Plasma concentration of 14C decreased from 9.2% at 0.5 h to 4.7% at 6.0 h. 2 plasma elimination rates were observed, with half-lives of 2.6 and 14.9 h, respectively. Approximately 80% of the administered 14C activity was excreted in feces and urine by 24 h after administration. A second group of rats was pretreated with 50 mg/kg of citrinin, i.p., 4 days prior to administration of 3 mg/kg [14C]citrinin, i.v. 30% of the pretreated animals died and the remaining animals were divided into 2 groups on day 4 after pretreatment; rats which were "nephrotoxic" and rats which had "recovered" from the initial insult of citrinin. Proteinuria and glucosuria as well as enhanced urine output were observed in "nephrotoxic" rats 4 days after pretreatment. 24 h after [14C]citrinin, only 13% of 14C activity was detected in the urine of "nephrotoxic" rats. The plasma disappearance curve had 2 elimination rates, with half-lives of 0.6 and 14.1 h. "Nephrotoxic" rats retained 7.5% of the administered radioactivity in the liver compared to 1.3% in the "recovered" rats 24 h after the tracer dose and 47% of the radioactivity was either excreted in feces or in the colon contents after 72 h compared to 17.5% in "recovered" rats. Extraction of urine samples from "nephrotoxic" and "recovered" rats with chloroform suggested increased water soluble metabolites of citrinin in the urine from "nephrotoxic" rats. These data also suggested that in normal rats the kidneys are the major route of elimination of citrinin and its metabolite(s) while in rats rendered nephrotoxic by citrinin pretreatment, elimination is more dependent on hepatic excretion.
测定了雄性大鼠静脉注射[¹⁴C]桔青霉素(3mg/kg)后的放射性分布与排泄情况。给药后0.5小时,肝脏和肾脏中放射性占总放射性的最大值分别为14.7%和5.6%,到6小时时,肝脏中降至7.5%,肾脏中降至4.7%。¹⁴C的血浆浓度从0.5小时时的9.2%降至6.0小时时的4.7%。观察到血浆有两个消除速率,半衰期分别为2.6小时和14.9小时。给药后24小时,约80%的¹⁴C活性经粪便和尿液排出。第二组大鼠在静脉注射3mg/kg[¹⁴C]桔青霉素前4天,腹腔注射50mg/kg桔青霉素进行预处理。30%的预处理动物死亡,其余动物在预处理后第4天分为两组:“肾毒性”大鼠和从桔青霉素初始损伤中“恢复”的大鼠。预处理后4天,“肾毒性”大鼠出现蛋白尿、糖尿以及尿量增加。[¹⁴C]桔青霉素给药24小时后,“肾毒性”大鼠尿液中仅检测到13%的¹⁴C活性。血浆消失曲线有两个消除速率,半衰期分别为0.6小时和14.1小时。“肾毒性”大鼠在示踪剂量给药24小时后,肝脏中保留了7.5%的给药放射性,而“恢复”大鼠为1.3%;72小时后,47%的放射性经粪便或结肠内容物排出,“恢复”大鼠为17.5%。用氯仿提取“肾毒性”和“恢复”大鼠的尿液样本表明,“肾毒性”大鼠尿液中桔青霉素的水溶性代谢物增加。这些数据还表明,在正常大鼠中,肾脏是桔青霉素及其代谢物的主要排泄途径,而在经桔青霉素预处理而产生肾毒性的大鼠中,排泄更多地依赖于肝脏排泄。