Comparison of the protective effects of amifostine and dexrazoxane against the toxicity of doxorubicin in spontaneously hypertensive rats

被引:93
作者
Herman, EH
Zhang, J
Chadwick, DP
Ferrans, VJ
机构
[1] US FDA, Div Appl Pharmacol Res HFD910, Ctr Drug Evaluat & Res, Laurel, MD 20708 USA
[2] NHLBI, Pathol Sect, NIH, Bethesda, MD 20892 USA
关键词
doxorubicin; cardiomyopathy; nephrotoxicity; amifostine; dexrazoxane;
D O I
10.1007/s002800050048
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To compare the protective effects of amifostine and dexrazoxane against the chronic toxicity induced by doxorubicin in spontaneously hypertensive rats (SHR). Methods: The animals were pretreated with amifostine (200 mg/kg, i.p.), dexrazoxane (25 mg/kg, i.p.) or saline 30 min before the administration of doxorubicin (1 mg/kg, i.v.), once-weekly for 12 weeks. Control animals received similar amounts of amifostine or saline. The SHR underwent necropsy examination 1 week after the last dosing, and cardiac, renal, and gastrointestinal lesions were graded semiquantitatively. Results: Amifostine and dexrazoxane provided equal degrees of protection against the renal toxicity of doxorubicin. However, dexrazoxane was more cardioprotective than amifostine, and prevented the mortality induced by doxorubicin. This mortality was not decreased by pretreatment with amifostine. The loss of body weight caused by doxorubicin was actually worsened by coadministration of amifostine. Conclusions: Compared to dexrazoxane, amifostine provided a comparable degree of protection against the nephrotoxicity of doxorubicin, but was less cardioprotective and did not prevent the mortality and loss of body weight produced by doxorubicin. These differences may be related to the fact that amifostine may act as a scavenger of reactive oxygen species, whereas dexrazoxane may prevent their formation.
引用
收藏
页码:329 / 334
页数:6
相关论文
共 40 条
[1]  
BERTAZZOLI C, 1979, CANCER TREAT REP, V63, P1877
[2]  
BERTELLI R, 1991, IN VITRO CELL DEV B, V27, P799
[3]  
BHANUMATHI P, 1992, BIOCHEM ARCH, V8, P335
[4]  
Billingham ME, 1991, CARDIOVASC PATHOL, P1465
[5]   ADVERSE-EFFECTS OF THE RADIOPROTECTOR WR2721 [J].
CAIRNIE, AB .
RADIATION RESEARCH, 1983, 94 (01) :221-226
[6]  
Capizzi RL, 1996, SEMIN ONCOL, V23, P2
[7]  
Dobric Silva, 1998, Journal of Environmental Pathology Toxicology and Oncology, V17, P291
[8]  
DOROSHOW J H, 1991, Proceedings of the American Association for Cancer Research Annual Meeting, V32, P332
[9]   Cardioprotection of rat heart myocytes with amifostine (Ethyol(R)) and its free thiol, WR-1065, in vitro [J].
Dorr, RT ;
Lagel, K ;
McLean, S .
EUROPEAN JOURNAL OF CANCER, 1996, 32A :S21-S25
[10]   PROSPECTIVE RANDOMIZED STUDY OF THE ROLE OF N-ACETYL CYSTEINE IN REVERSING DOXORUBICIN-INDUCED CARDIOMYOPATHY [J].
DRESDALE, AR ;
BARR, LH ;
BONOW, RO ;
MATHISEN, DJ ;
MYERS, CE ;
SCHWARTZ, DE ;
DANGELO, T ;
ROSENBERG, SA .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1982, 5 (06) :657-663