Effect of cis-diamminedichloroplatinum(II) combined with whole body hyperthermia on renal injury

• Published in: Cancer research (Chicago, Ill.) Ill.), 1988-01, Vol.48 (2), p.440-446
• Main Authors: WONDERGEM, J, BULGER, R. E, STREBEL, F. R, NEWMAN, R. A, TRAVIS, E. L, STEPHENS, L. C, BULL, J. M. C
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Blood Urea Nitrogen; Cisplatin - therapeutic use; Cisplatin - toxicity; Combined Modality Therapy; Creatinine - blood; Drug toxicity and drugs side effects treatment; Female; Fibrosarcoma - therapy; Hyperthermia, Induced; Kidney - drug effects; Kidney - pathology; Medical sciences; Necrosis; Pharmacology. Drug treatments; Rats; Rats, Inbred F344; Time Factors; Toxicity: urogenital system
• ISSN: 0008-5472; 1538-7445

The effect of whole body hyperthermia (WBH) on cis-diamminedichloroplatinum (II) (DDP) induced renal toxicity and antitumor effect was studied using a F344 rat model. Renal injury at 5 and 14 days after treatment was evaluated using animal mortality, renal functional assays (blood urea nitrogen, creatinine), and histopathological methods. WBH (120 min at 41.5 degrees C) enhanced both antitumor effects and toxic side effects. The latter included increased mortality, increased blood urea nitrogen and creatinine levels, and increased renal damage. After simultaneous treatment with WBH and DDP, thermal enhancement ratios (TER) for renal damage between 2.5 and 3.0 were calculated. The histopathological changes observed in the kidney after DDP alone or combined with WBH were primarily found in the proximal pars recta tubules (S3 segment) in the outer stripe of the outer medulla. There was no qualitative difference in tubular damage between rats treated with DDP alone or those treated with DDP combined with WBH. However, at a fixed DDP dose, damage in the combined treatment modality group was significantly greater than in the DDP-only treated group.