Suzuki T, Yamamoto H, Iwasaki T, Okamoto S, Iizuka T, Kanda H, Murata K
Gan To Kagaku Ryoho. 1984 Oct;11(10):2170-6.
The cardiotoxicities of 4'-epidoxorubicin (4-epiDX) and doxorubicin (DX) were compared in rabbits. Thirty-one male NZW rabbits weighing 2.4 to 2.6 kg were used for each compound and 15 were kept as controls. DX or 4'-epiDX was administered intravenously with a dose of 0.8 mg/kg for 3 consecutive days a week for 5-10 weeks. Rabbits were sacrificed at 5, 8 and 10 weeks after initial administration. Under nembutal anesthesia, electrocardiogram, phonocardiogram and carotidgram were recorded. Light and electron microscopic studies of the heart were performed according to conventional methods. Myocardial alterations were semi-quantitatively evaluated with light microscopy, using a modified grading system derived from Bertazzoli. Twelve of the DX-treated rabbits and 4 of the 4'-epiDX-treated rabbits died after 5 weeks or later. In the electrocardiogram study, ST-T changes were less frequently observed in rabbits treated with 4'-epiDX than those with DX. Significant increases of PEP/LVET were observed in rabbits treated with DX for 8 and 10 weeks, similar increases were only observed while in rabbits treated with 4'-epiDX for 10 weeks. Histologically, both drugs produced myocardial degeneration and necrosis. The lesions were characterized by multiple vacuolization of myocardial cells, atrophy of myocardial cells, interstitial edema and fibrosis. Myocardial alterations induced by 4'-epiDX were qualitatively similar to those induced by DX, but were much less severe at the same cumulative dose. These results demonstrate that 4'-epiDX is less cardiotoxic than DX.
在兔子身上比较了4'-表阿霉素(4-epiDX)和阿霉素(DX)的心脏毒性。每种化合物使用31只体重为2.4至2.6千克的雄性新西兰白兔,15只作为对照。以0.8毫克/千克的剂量静脉注射DX或4'-epiDX,每周连续3天,共5至10周。在初次给药后5、8和10周处死兔子。在戊巴比妥麻醉下,记录心电图、心音图和颈动脉图。按照常规方法对心脏进行光镜和电镜研究。使用源自Bertazzoli的改良分级系统,通过光镜对心肌改变进行半定量评估。12只接受DX治疗的兔子和4只接受4'-epiDX治疗的兔子在5周或更晚后死亡。在心电图研究中,4'-epiDX治疗的兔子比DX治疗的兔子更少观察到ST-T改变。接受DX治疗8周和10周的兔子观察到PEP/LVET显著增加,而仅在接受4'-epiDX治疗10周的兔子中观察到类似增加。组织学上,两种药物均引起心肌变性和坏死。病变的特征是心肌细胞多处空泡化、心肌细胞萎缩、间质水肿和纤维化。4'-epiDX诱导的心肌改变在性质上与DX诱导的相似,但在相同累积剂量下严重程度要低得多。这些结果表明,4'-epiDX的心脏毒性低于DX。