Studies on the urotoxicity of oxazaphosphorine cytostatics and its prevention—I

Norbert Brock, Jörg Pohl, Jurij Stekar
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引用次数: 108

Abstract

The urotoxic potency of various (mainly alkylating) drugs was studied in an extensive series of experiments. It was found that damage to the kidneys and to the efferent urinary tract (haemorrhagic cystitis) is a specific side effect of compounds possessing the oxazaphosphorine ring. This effect is due to the renal excretion of toxic metabolites. The only carriers of urotoxicity are the renally eliminated fractions of the 4-hydroxy-oxazaphosphorines and acrolein which is formed spontaneously therefrom. Other oxazaphosphorine metabolites and breakdown products such as the directly alkylating phosphoric acid diamides, 4-keto-derivatives and carboxyderivatives, have at most only a very slight urotoxic potency. The relationships between the chemical structure and the urotoxicity have been clarified in the group of oxazaphosphorines. Using a standardised test model (rat) the urotoxic side effects of cytostatics were studied experimentally and were measured quantitatively. The urotoxic effects were found to be dose- and concentration-dependent and also showed a marked dependence on the pH. The manifestations of inflammation were more pronounced in an alkaline than in an acidic milieu.

奥扎磷细胞抑制剂的尿毒性及其预防研究——Ⅰ
在一系列广泛的实验中研究了各种(主要是烷化)药物的尿毒性。研究发现,对肾脏和传出尿路的损伤(出血性膀胱炎)是具有恶磷环的化合物的一种特殊副作用。这种影响是由于毒性代谢产物的肾脏排泄。唯一的尿毒性载体是4-羟基氧杂磷和丙烯醛的经肾清除的部分,它们是由它们自发形成的。其他恶磷代谢产物和分解产物,如直接烷基化磷酸二酰胺、4-酮衍生物和羧基衍生物,至多只有非常轻微的尿毒性。已经阐明了氧杂磷类化合物的化学结构与尿毒性之间的关系。使用标准化试验模型(大鼠)对细胞抑制剂的尿毒副作用进行了实验研究,并进行了定量测量。尿毒作用是剂量和浓度依赖性的,也表现出对pH的显著依赖性。炎症的表现在碱性环境中比在酸性环境中更明显。
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