Genotoxicity of pyrrolizidine alkaloids

被引:157
作者
Chen, Tao [1 ]
Mei, Nan [1 ]
Fu, Peter P. [1 ]
机构
[1] US FDA, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
关键词
pyrrolizidine alkaloid; genotoxicity; mutation; DNA damage; carcinogenesis; mutational signature; VENO-OCCLUSIVE DISEASE; DNA ADDUCT FORMATION; BIG BLUE RATS; HEPATOCYTE MICRONUCLEUS ASSAY; HEPATIC VENOOCCLUSIVE DISEASE; COMFREY SYMPHYTUM-OFFICINALE; TRADITIONAL MEDICINAL HERBS; BONE-MARROW CELLS; S-PHASE SYNTHESIS; FORMATION IN-VIVO;
D O I
10.1002/jat.1504
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Pyrrolizidine alkaloids (PAs) are common constituents of many plant species around the world. PA-containing plants are probably the most common poisonous plants affecting livestock and wildlife. They can inflict harm to humans through contaminated food sources, herbal medicines and dietary supplements. Half of the identified PAs are genotoxic and many of them are tumorigenic. The mutagenicity of PAs has been extensively studied in different biological systems. Upon metabolic activation, PAs produce DNA adducts, DNA cross-linking, DNA breaks, sister chromatid exchange, micronuclei, chromosomal aberrations, gene mutations and chromosome mutations in vivo and in vitro. PAs induced mutations in the cll gene of rat liver and in the p53 and K-ras genes of mouse liver tumors. It has been suggested that all PAs produce a set of (+/-)-6,7-dihydro-7-hydroxy-1-hydroxymethyl-5H-pyrrolizine-derived DNA adducts and similar types of gene mutations. The signature types of mutations are G:C -> T:A transversion and tandem base substitutions. Overall, PAs are mutagenic in vivo and in vitro and their mutagenicity appears to be responsible for the carcinogenesis of PAs. Published in 2010 by John Wiley & Sons, Ltd.
引用
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页码:183 / 196
页数:14
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