Solomonson L P, Halabrin P R
Cancer Res. 1981 Feb;41(2):570-2.
Adriamycin ws tested as a possible inhibitor of cardiac sodium-potassium-activated adenosine triphosphatase (Na-K-ATPase). At concentrations of 10(-4) M and lower, Adriamycin had no effect upon either ouabain-sensitive (Na-K-ATPase) or ouabain-insensitive adenosine triphosphatase activity in homogenates and microsomal fractions of cardiac tissue from several different species. Adriamycin inhibited adenosine triphosphatase activity at a concentration of 10(-3) M, but this was due to the inhibition of ouabain-insensitive adenosine triphosphatase rather than to inhibition of Na-K-ATPase. Under no condition was an inhibition of Na-K-ATPase activity by Adriamycin observed. These conditions included preincubation of the enzyme with Adriamycin, chelation of Ca2+, addition of reduced nicotinamide adenine dinucleotide phosphate, and variation of buffer and pH. It was concluded that Na-K-ATPase is not a likely site of Adriamycin-induced cardiotoxicity.
对阿霉素作为心脏钠钾激活三磷酸腺苷酶(Na-K-ATP酶)的一种可能抑制剂进行了测试。在浓度为10⁻⁴M及更低时,阿霉素对来自几种不同物种的心脏组织匀浆和微粒体部分中的哇巴因敏感(Na-K-ATP酶)或哇巴因不敏感的三磷酸腺苷酶活性均无影响。阿霉素在浓度为10⁻³M时抑制三磷酸腺苷酶活性,但这是由于对哇巴因不敏感的三磷酸腺苷酶的抑制,而非对Na-K-ATP酶的抑制。在任何条件下均未观察到阿霉素对Na-K-ATP酶活性的抑制作用。这些条件包括酶与阿霉素的预温育、Ca²⁺的螯合、还原型烟酰胺腺嘌呤二核苷酸磷酸的添加以及缓冲液和pH值的变化。得出的结论是,Na-K-ATP酶不太可能是阿霉素诱导心脏毒性作用的位点。