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阿霉素及相关蒽环类抗生素对质膜NADH脱氢酶的抑制作用。

Inhibition of plasma membrane NADH dehydrogenase by adriamycin and related anthracycline antibiotics.

作者信息

Sun I L, Crane F L, Löw H, Grebing C

出版信息

J Bioenerg Biomembr. 1984 Jun;16(3):209-21. doi: 10.1007/BF00751050.

Abstract

Doxorubicin (adriamycin) is cytotoxic to cells, but the biochemical basis for this effect is unknown, although intercalation with DNA has been proposed This study suggests that the cytotoxicity of this drug may be due to inhibition of the plasma membrane redox system, which is involved in the control of cellular growth. Concentrations between 10(-6) - 10(-7) M adriamycin inhibit plasma membrane redox reactions greater than 50%. AD32, a form of adriamycin which does not intercalate with DNA, but is cytotoxic, also inhibits the plasma membrane redox system. Thus, the cytotoxic effects of adriamycin, which limit its use as a drug, may be based on the inhibition of a transplasma membrane dehydrogenase involved in a plasma membrane redox system.

摘要

阿霉素(阿德里亚霉素)对细胞具有细胞毒性,但其产生这种作用的生化基础尚不清楚,尽管有人提出它可嵌入DNA。本研究表明,这种药物的细胞毒性可能是由于抑制了参与细胞生长控制的质膜氧化还原系统。10^(-6) - 10^(-7) M浓度的阿霉素对质膜氧化还原反应的抑制率超过50%。AD32是阿霉素的一种形式,它不与DNA嵌入,但具有细胞毒性,也能抑制质膜氧化还原系统。因此,限制阿霉素作为药物使用的细胞毒性作用,可能是基于对参与质膜氧化还原系统的一种跨质膜脱氢酶的抑制作用。

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