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普萘洛尔增强阿霉素的毒性作用。

Potentiation of the toxicity of adriamycin by propranolol.

作者信息

Choe J Y, Combs A B, Folkers K

出版信息

Res Commun Chem Pathol Pharmacol. 1978 Sep;21(3):577-80.

PMID:705032
Abstract

Both propranolol and adriamycin are biochemically known to inhibit mitochondrial CoQ10-enzymes of myocardial tissue in vitro. Both propranolol and adriamycin are clinically known to cause cardiotoxicity. At two dose levels of propranolol which caused no deaths to mice when administered alone, significant potentiation (p less than 0.01) of the lethality of adriamycin to mice was observed. These data, projected to the clinical situation, seem to contraindicate the administration of the beta-blocker, propranolol, for the hypertension of a cancer patient who is being treated with adriamycin.

摘要

已知普萘洛尔和阿霉素在体外均可抑制心肌组织中的线粒体辅酶Q10-酶。临床已知普萘洛尔和阿霉素均会引起心脏毒性。在单独给药时对小鼠无致死作用的两个普萘洛尔剂量水平下,观察到阿霉素对小鼠的致死性有显著增强作用(p小于0.01)。这些数据外推至临床情况后,似乎表明正在接受阿霉素治疗的癌症患者高血压时,禁忌使用β受体阻滞剂普萘洛尔。

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