Solaini G, Ronca G, Bertelli A
Drugs Exp Clin Res. 1985;11(8):533-7.
A set of three novel anthracyclines, active as antitumour agents, has been examined for their possible effects on rat heart mitochondrial respiration. The in vitro inhibiting effects of the compounds have been compared with that of the older doxorubicin. Aclacinomycin was generally more inhibitory than doxorubicin, 4'-epi-doxorubicin and 4'-epi-tetrahydropyranyl-adriamycin, with both succinate and NAD+-linked substrates. Attempts to prevent anthracycline from inhibiting the succinate oxidase activity by means of adding exogenous coenzyme Q10 gave encouraging results, the inhibiting effect being in fact reduced.
一组三种新型蒽环类药物作为抗肿瘤剂具有活性,已对其对大鼠心脏线粒体呼吸的可能影响进行了研究。已将这些化合物的体外抑制作用与旧的阿霉素的抑制作用进行了比较。阿克拉霉素通常比阿霉素、4'-表阿霉素和4'-表四氢吡喃基阿霉素对琥珀酸和NAD+连接底物的抑制作用更强。尝试通过添加外源性辅酶Q10来防止蒽环类药物抑制琥珀酸氧化酶活性,结果令人鼓舞,抑制作用实际上有所降低。