Harauchi T, Hirata M
Shionogi Research Laboratories, Shionogi & Co., Ltd., Osaka, Japan.
Toxicol Lett. 1993 Jan;66(1):35-46. doi: 10.1016/0378-4274(93)90077-b.
In vitro toxicity of p-phenylenediamine derivatives and adriamycin were examined using cultured rat myofibers prepared by the selective plating method, with slight modification. When the myofibers were cultured for 2 days with 100 microM N,N,N',N'-tetramethyl p-phenylenediamine, atrophy and/or swelling of the cells were observed, and the toxic effect was reduced as the number of N-methyl groups in the phenylenediamine molecule was decreased. Adriamycin, at concentrations of greater than 0.25 microM, caused cell injury. Decline of cellular creatine phosphokinase activities generally preceded the apparent morphological changes. The primary culture of rat myofibers responded sensitively to the agents which were myotoxic in vivo.
采用选择性铺板法制备大鼠肌纤维培养物,并略作修改,以此检测对苯二胺衍生物和阿霉素的体外毒性。当肌纤维与100微摩尔/升的N,N,N',N'-四甲基对苯二胺一起培养2天时,可观察到细胞萎缩和/或肿胀,且随着对苯二胺分子中N-甲基基团数量的减少,毒性作用减弱。阿霉素浓度大于0.25微摩尔/升时会导致细胞损伤。细胞肌酸磷酸激酶活性的下降通常先于明显的形态学变化出现。大鼠肌纤维的原代培养物对体内具有肌毒性的药物反应敏感。