Myers C E, McGuire W P, Liss R H, Ifrim I, Grotzinger K, Young R C
Science. 1977 Jul 8;197(4299):165-7. doi: 10.1126/science.877547.
The antitumor antibiotic, adriamycin, induces severe cardiac toxicity associated with peroxidation of cardiac lipids in mice. Both this lipid peroxidation and cardiac toxicity of adriamycin are reduced by prior treatment of the animals with the free radical scavenger tocopherol. Such treatment with tocopherol does not, however, alter the magnitude or duration of the adriamycin-induced suppression of DNA synthesis in P388 ascites tumor, nor does it diminish the antitumor responsiveness of P388 ascites tumor. These results suggest that adriamycin has at least two mechanisms of tissue damage: one, which involves lipid peroxidation, is blocked by tocopherol and results in cardiac toxicity; the other, which involves binding to DNA, is not antagonized by tocopherol and is responsible for tumor response.
抗肿瘤抗生素阿霉素可在小鼠中诱发与心脏脂质过氧化相关的严重心脏毒性。用自由基清除剂生育酚预先处理动物,可降低阿霉素引起的这种脂质过氧化和心脏毒性。然而,生育酚的这种处理并不会改变阿霉素诱导的对P388腹水瘤DNA合成的抑制程度或持续时间,也不会降低P388腹水瘤的抗肿瘤反应性。这些结果表明,阿霉素至少有两种组织损伤机制:一种涉及脂质过氧化,可被生育酚阻断并导致心脏毒性;另一种涉及与DNA结合,不受生育酚拮抗,是肿瘤反应的原因。