Herman E H, Ferrans V J
Cancer Chemother Pharmacol. 1986;16(2):102-6. doi: 10.1007/BF00256157.
The long-term protective effect of ICRF-187 against chronic daunorubicin cardiotoxicity was examined. Rabbits were given 3.2 mg daunorubicin/kg, with or without pretreatment with 25 mg ICRF-187/kg, once every 3 weeks over an 18-week period (6 doses). The experiment was terminated 3 months after the last treatment. At this time, all seven rabbits given daunorubicin alone had evidence of myocardial alterations ranging from minimal (2 animals) to mild (5 animals). Pretreatment with ICRF-187 caused a significant reduction in both the incidence and the severity of cardiac lesions. Hearts from the majority (5 of 7) of animals given the combination of ICRF-187 and daunorubicin were normal; myocardial alterations were minimal in the remaining rabbits treated with ICRF-187. In previous studies ICRF-187 was found to cause a reduction in cardiotoxicity 1-3 weeks after the final anthracycline dose. The results of the present study demonstrate that pretreatment with ICRF-187 provides prolonged protection against the cardiomyopathy, as opposed to producing only a delay in the appearance of cardiac alterations.
研究了ICRF-187对柔红霉素慢性心脏毒性的长期保护作用。给兔子注射3.2mg柔红霉素/千克,有或没有预先注射25mg ICRF-187/千克,在18周内每3周注射一次(共6剂)。在最后一次治疗后3个月终止实验。此时,所有7只单独注射柔红霉素的兔子都有心肌改变的证据,从轻微(2只动物)到轻度(5只动物)。预先注射ICRF-187可使心脏病变的发生率和严重程度显著降低。大多数(7只中的5只)接受ICRF-187和柔红霉素联合治疗的动物心脏正常;其余接受ICRF-187治疗的兔子心肌改变轻微。在先前的研究中发现,ICRF-187在最后一剂蒽环类药物后1-3周可降低心脏毒性。本研究结果表明,预先注射ICRF-187可对心肌病提供长期保护,而不仅仅是延迟心脏改变的出现。