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阿霉素诱导的心力衰竭:机制与调节

Adriamycin-induced heart failure: mechanism and modulation.

作者信息

Singal P K, Li T, Kumar D, Danelisen I, Iliskovic N

机构信息

Institute of Cardiovascular Sciences, St. Boniface General Hospital Research Centre and Department of Physiology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.

出版信息

Mol Cell Biochem. 2000 Apr;207(1-2):77-86. doi: 10.1023/a:1007094214460.

Abstract

Adriamycin (doxorubicin) is one of the most effective chemotherapeutic agents against a variety of cancers, but its usefulness is seriously curtailed by the risk of developing heart failure. Available laboratory evidence suggests that an increase in oxidative stress, brought about by increased free radical production and decreased myocardial endogenous antioxidants, plays an important role in the pathogenesis of heart failure. Adriamycin-induced apoptosis and hyperlipidemia may also be involved in the process. Probucol, a lipid-lowering drug and an antioxidant, completely prevents the occurrence of heart failure by reducing oxidative stress as well as by the modulation of apoptosis and high lipid concentrations. Thus, combined therapy with adriamycin and probucol has a high potential for optimizing the treatment of cancer patients.

摘要

阿霉素(多柔比星)是治疗多种癌症最有效的化疗药物之一,但其效用因发生心力衰竭的风险而严重受限。现有实验室证据表明,自由基产生增加和心肌内源性抗氧化剂减少所导致的氧化应激增加,在心力衰竭的发病机制中起重要作用。阿霉素诱导的细胞凋亡和高脂血症也可能参与这一过程。普罗布考是一种降脂药物和抗氧化剂,通过降低氧化应激以及调节细胞凋亡和高脂浓度,可完全预防心力衰竭的发生。因此,阿霉素与普罗布考联合治疗在优化癌症患者治疗方面具有很大潜力。

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