庆大霉素致大鼠子宫内肾毒性。

J P Mallié, H Gerard, A Gerard
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引用次数: 0

摘要

众所周知,氨基苷会导致肾毒性。在怀孕母亲给药后,正在发育的肾脏在子宫内被改变的可能性已被调查。我们在怀孕大鼠器官发生期(第7-11天)和肾小球分化期(第14-18天)给予庆大霉素(75 mg/kg/天)。一组未怀孕的女性也在同一时期和每天同一时间接受治疗。庆大霉素治疗的母亲只有轻微的血液生物学变化,没有急性肾功能衰竭,而未怀孕的女性有高肌酐血症。在含有新生儿完全形成的肾单位的深皮质区,庆大霉素组出现的分化肾小球比对照组少。此外,在光镜和电镜下,肾小球和近端小管在髓旁皮质显示肾毒性的证据。子宫内氨基苷肾毒性的发现表明,在怀孕期间给予庆大霉素可能对胎儿肾脏有毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In-utero gentamicin-induced nephrotoxicity in rats.

Aminosides lead to a well-known nephrotoxicity. The possibility of the developing kidney being altered in utero after the pregnant mother's administration has been investigated. We gave gentamicin (75 mg/kg/day) to pregnant rats during periods of organogenesis (days 7-11) and the beginning of glomeruli differentiation (days 14-18). A group of nonpregnant females was also treated for the same period and at the same time each day. Gentamicin-treated mothers presented only minor modifications of the blood biology with no acute renal failure when treated nonpregnant females have a hypercreatininemia. The deep cortical area, containing the fully formed nephrons of neonates, presented less glomeruli that were differentiated in the gentamicin group than in the control group. Moreover with both light and electron microscopy, glomeruli and proximal tubules showed evidences of nephrotoxicity in the juxtamedullary cortex. This finding of an in utero aminoside nephrotoxicity demonstrates the possible toxicity of gentamicin on fetus kidneys when given during the pregnancy.

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