Influence of silymarin and its flavonolignans on doxorubicin-iron induced lipid peroxidation in rat heart microsomes and mitochondria in comparison with quercetin

被引:56
|
作者
Psotová, J
Chlopcíková, S
Grambal, F
Simánek, V
Ulrichová, J
机构
[1] Palacky Univ, Fac Med, Inst Med Chem & Biochem, Olomouc 77515, Czech Republic
[2] Palacky Univ, Fac Sci, Inst Inorgan & Phys Chem, Olomouc 77100, Czech Republic
关键词
silymarin; silybin; silydianin; silychristin; quercetin; rat heart microsomes; rat heart mitochondria; iron; doxorubicin; lipid peroxidation; DPPH colour reduction; peak oxidation potentials;
D O I
10.1002/ptr.811
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Silymarin, an extract of Silybum marianum seeds, and the constituent flavonolignans silybin, silydianin and silychristin, as well as the flavonol quercetin, protected rat heart microsomes and mitochondria against iron-dependent doxorubicin induced lipid peroxidation. Quercetin was found to be more potent than either silymarin or its three constituents, whose cytoprotectivity was comparable. The radical scavenging activity of the compounds was investigated using a DPPH colour reduction assay and cyclic voltametry to assess their antioxidant activities. In contrast to quercetin, silybin, silydianin and silychristin did not chelate iron in aqueous solution. The results suggest that silymarin may prevent doxorubicin-mediated damage to rat heart membrane primarily through a free radical scavenging mechanism. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:S63 / S67
页数:5
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