Reese J B, Shirhatti V, Singh Y, Krishna G
Toxicol Appl Pharmacol. 1987 Mar 30;88(1):105-12. doi: 10.1016/0041-008x(87)90274-2.
Daunomycin and adriamycin are widely used antitumor agents which induce dose-dependent cardiotoxicity. The mechanisms by which daunomycin causes cardiotoxicity have been investigated in neonatal rat cardiac myocytes maintained in tissue culture. Daunomycin inhibited the uptake of adenine, amino acids, and deoxyglucose in a dose-dependent fashion. The uptake of both adenine and methionine was inhibited without any delay while the glucose uptake (deoxyglucose) was inhibited after a delay of 2 hr. Since daunomycin affected the uptake of both adenine and amino acids without any delay and since daunomycin did not affect the incorporation of adenine into nucleotide and amino acids into proteins once these were transported into the cell, it is possible the daunomycin exerted these effects by acting directly on the cell membrane. Thus, one of the early toxic manifestations of anthracycline antibiotics may be on the transport of nutrients such as amino acids, glucose, and adenine.
柔红霉素和阿霉素是广泛使用的抗肿瘤药物,它们会引发剂量依赖性心脏毒性。在组织培养中维持的新生大鼠心肌细胞中,对柔红霉素导致心脏毒性的机制进行了研究。柔红霉素以剂量依赖性方式抑制腺嘌呤、氨基酸和脱氧葡萄糖的摄取。腺嘌呤和蛋氨酸的摄取在没有任何延迟的情况下受到抑制,而葡萄糖摄取(脱氧葡萄糖)在延迟2小时后受到抑制。由于柔红霉素在没有任何延迟的情况下影响腺嘌呤和氨基酸的摄取,并且由于一旦这些物质被转运到细胞内,柔红霉素不会影响腺嘌呤掺入核苷酸以及氨基酸掺入蛋白质,所以柔红霉素可能是通过直接作用于细胞膜发挥这些作用的。因此,蒽环类抗生素的早期毒性表现之一可能在于对氨基酸、葡萄糖和腺嘌呤等营养物质的转运。