抗肿瘤药物阿霉素(ADM)对心肌线粒体F1F0-复合体呈现抑制而对F1-ATPase无抑制,这表明ADM可能是通过膜脂起作用的,适当浓度Mg2+能降低ADM对复合体的抑制.经 31P-NMR和标记荧光探针NBD-PE,DPH,MC-540以及内源荧光等的测定,结果表明ADM可能首先通过诱导F1F0膜脂形成非双层脂结构,继而影响了膜脂的堆积程度和流动性,进而引起F1F0-复合体酶蛋白构象的改变,最终导致酶活力的降低.Mg2+则可能由于与ADM竞争与心磷脂的结合,而对ADM引起F1F0的变化产生保护作用.
Adriamycin (ADM) is a widely used anticancer drug, but the chronic cardiotoxicity severely limits the use of it in the treatment of neoplastic disease. The experimental results obtained from F1F0-ATPase activity assay. 31P-NMR spectra measurement. fluorescent probe NBDPE detection. packing and fluidity of membrane lipids and intrinsic fluorescence measurements can be summarized as follows: ADM induces the phase transition of mitochondrial membrane lipids at first. as a consequence affecting on the lipid packing and fluidity of the lipid molecules and then influencing the conformation of the F1F0-ATPase and finally resuiting in the decreasing of the enzymatic activity. And Mg2+ can protect all the effects induced by ADM thus reducing the harmful effect of ADM.
林治焕,李生广,曹懋孙,陈云俊,封朝阳,邓君鹏. Mg2+对阿霉素引起心肌线粒体F1F0变化的保护[J].生物化学与生物物理进展,1994,21(1):61-66
复制生物化学与生物物理进展 ® 2025 版权所有 ICP:京ICP备05023138号-1 京公网安备 11010502031771号