Dantchev D, Slioussartchouk V, Paintrand M, Bourut C, Hayat M, Mathe G
C R Seances Soc Biol Fil. 1979;173(2):394-413.
Golden hamsters were submitted to i.p. administration during 4 weeks of 8 anthracyclines, adriamycin (ADM), detorubicin (DTR), daunorubicin (DNR), 4'-epi-adriamycin (eADM), adriamycin hydrochloride (ADMh), rubidazon (RBZ), aclacinomycin (ACM) and AD32, at doses equivalent to 3/4 of those which are optimally oncostatic on murine L1210 leukemia. The comparative study of the mortality, the electron microscopic (EM) alterations of the myocardium, and the light microscopic (EM) alterations of the myocardium, and the light microscopic (LM) lesions of the skin, show that ACM and AD32 are the least toxic drugs. EM detected almost no early lesions of myocardium in ACM treated animals, but, after 4 week's treatment, severe cardiac alterations appeared which, like those after AD32 treatment, are non lethal and reversible. Similarly. LM revealed no histologic changes in the skin following ACM and AD32 administrations, but pathologic alterations, atrophy and alopecia, were observed in animals receiving all other drugs.
将8种蒽环类药物,即阿霉素(ADM)、去甲柔红霉素(DTR)、柔红霉素(DNR)、4'-表阿霉素(eADM)、盐酸阿霉素(ADMh)、鲁比达唑(RBZ)、阿克拉霉素(ACM)和AD32,以相当于对小鼠L1210白血病产生最佳抑癌作用剂量的3/4给予金黄仓鼠,持续4周进行腹腔注射。对死亡率、心肌的电子显微镜(EM)改变、心肌的光学显微镜(LM)改变以及皮肤的光学显微镜(LM)损伤进行的比较研究表明,ACM和AD32是毒性最小的药物。电子显微镜检查发现,接受ACM治疗的动物心肌几乎没有早期损伤,但在治疗4周后,出现了严重的心脏改变,与AD32治疗后的情况一样,这些改变无致命性且可逆转。同样,光学显微镜检查显示,给予ACM和AD32后皮肤无组织学变化,但在接受所有其他药物治疗的动物中观察到了病理改变、萎缩和脱发。