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镁在体外对蒽环类药物毒性的保护作用。

Magnesium protection against anthracycline toxicity in vitro.

作者信息

Zdanowicz M M, Barletta M A

机构信息

College of Pharmacy and Allied Health, St. John's University, Jamaica, New York.

出版信息

Magnes Res. 1991 Jun;4(2):105-7.

PMID:1911091
Abstract

The clinical usefulness of the antitumour agents daunomycin (DAU) and adriamycin (ADR) is limited by their secondary cardiotoxicity. The anthracycline compounds have a number of detrimental effects on the biochemical and morphological integrity of the cardiac cell which may be related to the accumulation of cellular calcium. Using a model of spontaneously beating, cultured neonatal rat cardiomyocytes, we examined the cardioprotective role of magnesium during 2 hours of exposure to 10, 25 or 50 micrograms/ml DAU. A significant preservation of myocyte membrane integrity and cellular morphology was observed with the addition of equimolar magnesium. Magnesium opposes the actions of calcium in a number of tissues and it may be this calcium antagonist action that makes magnesium effective in DAU toxicity.

摘要

抗肿瘤药物柔红霉素(DAU)和阿霉素(ADR)的临床应用因其次发性心脏毒性而受到限制。蒽环类化合物对心脏细胞的生化和形态完整性有许多有害影响,这可能与细胞内钙的积累有关。利用自发搏动的培养新生大鼠心肌细胞模型,我们研究了在暴露于10、25或50微克/毫升柔红霉素2小时期间镁的心脏保护作用。加入等摩尔的镁后,观察到心肌细胞膜完整性和细胞形态得到了显著保护。镁在许多组织中拮抗钙的作用,可能正是这种钙拮抗剂作用使镁对柔红霉素毒性有效。

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