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首页> 外文期刊>British Journal of Cancer >Inhibitors of adriamycin-induced histamine release in vitro limit adriamycin cardiotoxicity in vivo
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Inhibitors of adriamycin-induced histamine release in vitro limit adriamycin cardiotoxicity in vivo

机译:阿霉素诱导的组胺抑制剂的体外释放限制了体内阿霉素的心脏毒性

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The activity of theophylline and disodium cromoglycate was tested on adriamycin-induced histamine release in vitro and on adriamycin cardiotoxicity in vivo. Both substances significantly inhibited the release of histamine induced by 100 micrograms ml-1 of adriamycin on rat peritoneal cells and produced significant protection against adriamycin-mediated acute and chronic cardiotoxicity in mice. N-acetylcysteine, a free radical scavenger, successfully used in the prevention of the cardiomyopathy, was also found to be an inhibitor of histamine release induced by adriamycin and compound 48/80 on rat peritoneal cells. This study further supports the hypothesis that the release of histamine may be involved in the pathogenesis of anthracycline cardiotoxicity.
机译:茶碱和色甘酸二钠的活性在体外由阿霉素诱导的组胺释放和在体内对阿霉素的心脏毒性进行了测试。两种物质均显着抑制了100微克ml-1的阿霉素诱导的大鼠腹膜细胞中组胺的释放,并对阿霉素介导的小鼠急性和慢性心脏毒性产生了明显的保护作用。 N-乙酰半胱氨酸是一种自由基清除剂,已成功用于预防心肌病,也被发现是阿霉素和化合物48/80诱导的大鼠腹膜细胞释放组胺的抑制剂。这项研究进一步支持了以下假设:组胺的释放可能与蒽环类药物的心脏毒性的发病机制有关。

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