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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Cytotoxicity and gene induction by some essential oils in the yeast Saccharomyces cerevisiae.
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Cytotoxicity and gene induction by some essential oils in the yeast Saccharomyces cerevisiae.

机译:酿酒酵母中某些精油的细胞毒性和基因诱导。

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In order to get an insight into the possible genotoxicity of essential oils (EOs) used in traditional pharmacological applications we tested five different oils extracted from the medicinal plants Origanum compactum, Coriandrum sativum, Artemisia herba alba, Cinnamomum camphora (Ravintsara aromatica) and Helichrysum italicum (Calendula officinalis) for genotoxic effects using the yeast Saccharomyces cerevisiae. Clear cytotoxic effects were observed in the diploid yeast strain D7, with the cells being more sensitive to EOs in exponential than in stationary growth phase. The cytotoxicity decreased in the following order: Origanum compactum>Coriandrum sativum>Artemisia herba alba>Cinnamomum camphora>Helichrysum italicum. In the same order, all EOs, except that derived from Helichrysum italicum, clearly induced cytoplasmic petite mutations indicating damage to mitochondrial DNA. However, no nuclear genetic events such as point mutations or mitotic intragenic or intergenic recombination were induced. The capacity of EOs to induce nuclear DNA damage-responsive genes was tested using suitable Lac-Z fusion strains for RNR3 and RAD51, which are genes involved in DNA metabolism and DNA repair, respectively. At equitoxic doses, all EOs demonstrated significant gene induction, approximately the same as that caused by hydrogen peroxide, but much lower than that caused by methyl methanesulfonate (MMS). EOs affect mitochondrial structure and function and can stimulate the transcriptional expression of DNA damage-responsive genes. The induction of mitochondrial damage by EOs appears to be closely linked to overall cellular cytotoxicity and appears to mask the occurrence of nuclear genetic events. EO-induced cytotoxicity involves oxidative stress, as is evident from the protection observed in the presence of ROS inhibitors such as glutathione, catalase or the iron-chelating agent deferoxamine.
机译:为了深入了解传统药理学中使用的精油(EOs)的潜在遗传毒性,我们测试了从药用植物Origanum compactum,Coriandrum sativum,Artemisia herba alba,Cinnamomum camphora(Ravintsara aromaa)和Helichrysum italicum提取的五种不同的油。 (Calendula officinalis)对啤酒酵母具有遗传毒性作用。在二倍体酵母菌株D7中观察到明显的细胞毒性作用,该细胞对EO的指数敏感性高于对静止生长期的敏感性。细胞毒性按以下顺序降低:紧凑牛至>小花ori>白蒿>樟树>蜡菊。以同样的顺序,除了从意大利蜡菊提取的外,所有EOs均明显诱导了胞质小突变,表明线粒体DNA受损。但是,没有诱导核遗传事件,如点突变或有丝分裂基因内或基因间重组。使用合适的RNC3和RAD51的Lac-Z融合菌株测试了EOs诱导核DNA损伤应答基因的能力,这两个菌株分别涉及DNA代谢和DNA修复。在等毒性剂量下,所有EOs均表现出显着的基因诱导,与过氧化氢引起的诱导大致相同,但远低于甲磺酸甲酯(MMS)引起的诱导。 EOs影响线粒体的结构和功能,并可以刺激DNA损伤反应基因的转录表达。 EOs诱导线粒体损伤似乎与总体细胞毒性密切相关,并且似乎掩盖了核遗传事件的发生。 EO诱导的细胞毒性涉及氧化应激,从存在ROS抑制剂(如谷胱甘肽,过氧化氢酶或铁螯合剂去铁胺)的情况下所观察到的保护作用可以明显看出。

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