[抗肿瘤Pt(II)和Pt(IV)配位化合物对大鼠的肾毒性和骨髓毒性]。

Archiv fur Geschwulstforschung Pub Date : 1989-01-01
U Horn, A Härtl, G Neuhaus, U Stöckel, H P Schröer, H Hoffmann
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引用次数: 0

摘要

与顺式ddp相比,在连续5天静脉给药最大耐受剂量后,评估了四种新的铂(II)和铂(IV)配合物在雄性大鼠中的急性肾毒性和骨髓毒性。第一次给药后第6、13、22天测定肾毒性指标:血、尿素氮、血清肌酐、尿量、尿糖、小管细胞排泄量。同一天测定的髓毒性参数包括白细胞、血小板、血红蛋白和红细胞压积。顺- ddp是最具肾毒性的化合物。新铂配合物的髓毒性除反式oddp外与顺式ddp相似。
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[Nephrotoxicity and myelotoxicity of antineoplastic Pt(II) and Pt(IV) coordination compounds in rats].

In comparison with cis-DDP four new platinum (II) and platinum (IV) complexes were evaluated for their acute nephrotoxic and myelotoxic potency in male rats following i.v. administration of maximum tolerated doses on 5 consecutive days. Parameters for nephrotoxicity determined on day 6, 13 and 22 after the first administration of the drugs included blood, urea nitrogen, serum creatinine, urine volume, urinary glucose and tubule cell excretion. Parameters for myelotoxicity determined on the same days included leucocytes, platelets, hemoglobin and hematocrit. Cis-DDP was found to be the most nephrotoxic compound. The myelotoxicity of the new platinum complexes appeared to be similar to that of cis-DDP with exception of trans-ODDP.

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