静脉注射头孢利定致大鼠肾损伤与24h尿酶测定的相关性。

E D Wachsmuth, H Wirz
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引用次数: 0

摘要

雄性大鼠单独置于代谢笼中,静脉注射头孢利定,连续采集24 h尿液样本;然后处死大鼠,取相应动物肾。测定尿液中蛋白质、氨基肽酶(AP)、碱性磷酸酶(aPP)、乳酸脱氢酶(LDH)和醛缩酶(ALD)的浓度,并在aPP染色切片中统计损伤近端小管的百分比。动物个体结果如下:(1)动物单独置于代谢笼后,尿酶浓度发生了较大但不系统的变化。6-10天后,酶达到稳态水平。(2)单次注射头孢利定后,尿LDH含量与近端小管损伤呈剂量依赖性,与小管损伤相关性最佳(r > 0.93),比正常值增加1000倍以上。(3)观察到大鼠肾脏对头孢利定的易感性的昼夜节律,在早上7点注射时反应最小,在晚上7点注射后反应最大。(4)亚急性毒性研究中,尿LDH在第2天高于单次剂量的程度,但在第3天下降,在8 ~ 10天(牺牲时间)后恢复正常水平。肾脏组织学基本正常。所研究的其他酶也恢复到正常水平。这表明存在某种适应机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relevance of enzyme evaluations in 24h urine to rat kidney injury caused by i.v. cephaloridine injection.

Male rats were housed singly in metabolic cages, injected i.v. with cephaloridine, 24 h urine samples collected successively; then the rats were killed for obtaining the kidneys of corresponding animals. The concentrations of protein, aminopeptidase (AP), alkaline phosphatase (aPP), lactic dehydrogenase (LDH), and aldolase (ALD) were determined in urine and the percentages of injured proximal tubules counted in sections stained for aPP. The results from individual animals were: (1) After placing animals singly in metabolic cages large but not systematic changes of urinary enzyme concentrations occurred. After 6-10 days the enzymes reached steady state levels. (2) After a single injection of cephaloridine a dose dependent injury of proximal tubules was observed, the urinary LDH content correlating best with the tubular injury (r greater than 0.93) and giving up to 1,000 fold increases above normal values. (3) A circadian rhythm of the susceptibility of rat kidney for cephaloridine was observed, the smallest response was seen when the animals were injected at 7 a.m. and the largest after injection at 7 p.m. (4) In subacute toxicity studies urinary LDH was increased on day 2 above the extent after a single dose, but declined on day 3 to reach normal levels after 8 to 10 days (time of sacrifice). The kidneys revealed practically normal histology. The other enzymes studied had also returned to normal values. This indicates some adaptation mechanism.

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