Scheffler Anne, Albrecht Annette E, Esch Harald L, Lehmann Leane
Institute of Pharmacy and Food Chemistry, Chair of Food Chemistry, University of Würzburg, Am Hubland, D-97074 Würzburg, Germany.
Institute of Pharmacy and Food Chemistry, Chair of Food Chemistry, University of Würzburg, Am Hubland, D-97074 Würzburg, Germany.
Toxicol Lett. 2015 Apr 16;234(2):81-91. doi: 10.1016/j.toxlet.2015.02.013. Epub 2015 Feb 19.
After consumption of red clover-based dietary supplements, plasma concentrations of the isoflavone irilone (IRI) equal that of the well-investigated daidzein. Since some isoflavones are genotoxic, the potential of IRI to induce mutations was investigated. Gene mutations were determined by hypoxanthine-guanine phosphoribosyltransferase (HPRT) assay and sequencing of mutant cDNA, chromosome and genome mutations by micronucleus assay complemented by immunochemical staining of centromere proteins and microtubules in cultured V79 cells. Cell proliferation was monitored by electronic cell counting, flow cytometry and fluorescence microscopy. IRI did not affect the mutant frequency in the Hprt locus but altered the mutation spectrum by increasing the proportion of deletions and decreasing that of base pair substitutions. Induction of chromosome mutations was supported by a slight but significant increase in the number of micronucleated cells containing chromosomal fragments despite activation of three cell cycle checkpoints possibly interfering with micronuclei formation. Moreover, IRI exhibited a strong aneugenic potential characterized by disrupted mitotic spindles, mitotic arrest, and asymmetrical cell divisions leading to chromosome loss, nuclear fragmentation as well as mitotic catastrophe. Thus, IRI might be another isoflavone to be taken into account in safety assessment of dietary supplements.
食用基于红三叶草的膳食补充剂后,异黄酮鸢尾酮(IRI)的血浆浓度与研究充分的大豆苷元相当。由于一些异黄酮具有基因毒性,因此对IRI诱导突变的潜力进行了研究。通过次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(HPRT)测定法确定基因突变,并对突变cDNA进行测序,通过微核测定法结合培养的V79细胞中着丝粒蛋白和微管的免疫化学染色来检测染色体和基因组突变。通过电子细胞计数、流式细胞术和荧光显微镜监测细胞增殖。IRI不影响Hprt基因座中的突变频率,但通过增加缺失比例和降低碱基对替换比例改变了突变谱。尽管三个细胞周期检查点被激活可能会干扰微核形成,但含有染色体片段的微核细胞数量略有但显著增加,这支持了染色体突变的诱导。此外,IRI表现出很强的非整倍体诱导潜力,其特征是有丝分裂纺锤体破坏、有丝分裂停滞以及不对称细胞分裂,导致染色体丢失、核碎裂以及有丝分裂灾难。因此,在膳食补充剂的安全性评估中,IRI可能是另一种需要考虑的异黄酮。