Villani F, Monti E, Piccinini F, Favalli L, Lanza E, Rozza Dionigi A, Poggi P
Tumori. 1986 Jun 30;72(3):323-9. doi: 10.1177/030089168607200315.
The aim of the present study was to evaluate the dose- and time-dependence of the effect displayed by doxorubicin (DXR) on the electrocardiogram (ECG) and to establish the relationship between structural alterations of the myocardium and ECG changes in rats administered DXR, at a dose of 1.5 or 3.0 mg/kg, every 3 days for a total of three administrations. The most interesting findings consisted of a dose-dependent, but reversible prolongation of the QRS complex, and in a dose-dependent and progressive irreversible increase in QaT and, in particular, in SaT duration. Furthermore, animals treated with the higher DXR dose showed a slight increase in serum K+ concentration and a significant decrease in serum Ca2+ levels. A good correlation was found between the morphologic score indicating the degree of observed tissue damage and SaT prolongation. These results therefore support the usefulness of measuring this ECG parameter for monitoring the development of DXR-induced cardiotoxicity in rats.
本研究的目的是评估阿霉素(DXR)对心电图(ECG)作用的剂量和时间依赖性,并确定在以1.5或3.0mg/kg的剂量、每3天给药一次、共给药三次的大鼠中,心肌结构改变与ECG变化之间的关系。最有趣的发现包括QRS波群呈剂量依赖性但可逆的延长,以及QaT尤其是SaT持续时间呈剂量依赖性和进行性不可逆增加。此外,接受较高DXR剂量治疗的动物血清K+浓度略有升高,血清Ca2+水平显著降低。观察到的组织损伤程度的形态学评分与SaT延长之间存在良好的相关性。因此,这些结果支持测量这一ECG参数对于监测大鼠中DXR诱导的心脏毒性发展的有用性。