具有多物种肾毒性作用的抗肿瘤药物cytembena (NSC-104801)的毒理学研究。

Cancer chemotherapy reports Pub Date : 1975-11-01
E J Gralla, G L Coleman, G W Osbaldiston, M Kashgarian, A M Jonas
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引用次数: 0

摘要

本研究以单次或每日静脉注射的方式研究了小猎犬犬和恒河猴的毒作用,注射剂量为12.5 - 200mg /kg/天,注射剂量为6.25 - 50mg /kg/天。肾小管损害是两个物种中主要的药物和剂量相关发现,临床表现为尿毒症、血清肌酐升高和蛋白尿。在肾脏中,给予最低毒性剂量的动物的原发性病变是细胞坏死和远端小管上皮脱屑。单剂量小鼠研究进一步表明,该药产生的更严重但类似的组织学变化,显示肾线粒体肿胀和破坏以及全身细胞肿胀,这是治疗后24小时建立的进行性亚细胞发育。狗和猴子在治疗后保留6周观察时发现肾小管上皮细胞再生,但功能恢复不一致。对淋巴组织的毒性作用是另一项发现。
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Toxicology studies with cytembena (NSC-104801), an antineoplastic agent with a multispecies nephrotoxic effect.

The toxic effects of cytembena in beagle dogs and rhesus monkeys were investigated with the drug given as single or daily iv injections in doses ranging from 12.5 to 200 mg/kg/day to dogs and 6.25 to 50 mg/kg/day to monkeys. Renal tubular damage was a major drug- and dose-related finding in both species and was clinically indicated by an accompanying uremia, elevated serum creatinine, and proteinuria. In the kidney, the primary lesion was cellular necrosis and desquamation of the distal tubular epithelium in animals given the lowest toxic doses. More severe but similar histologic changes produced by this drug were further characterized by single dose studies in mice which showed renal mitochondrial swelling and disruption plus generalized cell swelling as progressive, subcellular developments which were well established 24 hours after treatment. Cellular regeneration in the renal tubular epithelium was found in dogs and monkeys retained 6 weeks for observation after treatment, although functional recovery was inconsistent. A toxic effect to lymphoid tissue was an additional finding which is described.

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