首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Investigation of anti-oxidative, cytotoxic, DNA-damaging and DNA-protective effects of plant volatiles eugenol and borneol in human-derived HepG2, Caco-2 and VH10 cell lines.
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Investigation of anti-oxidative, cytotoxic, DNA-damaging and DNA-protective effects of plant volatiles eugenol and borneol in human-derived HepG2, Caco-2 and VH10 cell lines.

机译:研究植物挥发性丁香酚和冰片在人源性HepG2,Caco-2和VH10细胞系中的抗氧化,细胞毒性,DNA损伤和DNA保护作用。

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摘要

Plant volatiles, which can get into the human organism in food, medicines, or cosmetic preparations, frequently manifest antibacterial, antifungal, antiviral and other effects. We studied anti-oxidative, cytotoxic, genotoxic and possible DNA-protective effects of eugenol and borneol. Anti-oxidative activities of aqueous and ethanolic solutions of these two volatile compounds of plants were determined by a spectrophotometric method by the use of the stable DPPH radical. Borneol did not show any anti-oxidative activity even at the highest concentrations soluble in water or ethanol (<1000mM), while eugenol did manifest anti-oxidative activity, and at much lower concentrations (5-100 microM). The cytotoxicity of eugenol and borneol as well as their DNA-damaging effects and their influence on sensitivity of cells against the DNA-damaging effects of H(2)O(2) were investigated in three different cell lines, i.e. malignant HepG2 hepatoma cells, malignant Caco-2 colon cells, and nonmalignant human VH10 fibroblasts. The trypan-blue exclusion assay showed that in the three cell lines the cytotoxicity of eugenol was significantly higher than that of borneol. Single-cell gel electrophoresis revealed that borneol did not cause any DNA strand-breaks at the concentrations studied, but showed that all concentrations of eugenol (<600 microM) significantly increased the level of DNA breaks in human VH10 fibroblasts and to a lower degree in Caco-2 colon cells. The DNA-damaging effects of eugenol were not observed in metabolically active HepG2 hepatoma cells. Borneol and eugenol differed also with respect to their DNA-protective effects. While borneol protected HepG2 and, to a lesser extent, VH10 cells (but not Caco-2) against H(2)O(2)-induced DNA damage, eugenol either did not change the cellular sensitivity to H(2)O(2) (HepG2 cells) or it even increased the sensitivity (Caco-2 and VH10 cells). These results do not indicate any correlation between the DNA-protective and the anti-oxidative capacities of eugenol and borneol.
机译:在食品,药品或化妆品中可能进入人体的植物挥发物经常表现出抗菌,抗真菌,抗病毒和其他作用。我们研究了丁子香酚和冰片的抗氧化,细胞毒性,遗传毒性和可能的​​DNA保护作用。通过使用稳定的DPPH自由基,通过分光光度法测定了这两种挥发性植物化合物的水溶液和乙醇溶液的抗氧化活性。冰片即使在可溶于水或乙醇的最高浓度(<1000mM)下也没有表现出任何抗氧化活性,而丁香酚却在低得多的浓度(5-100 microM)下表现出抗氧化活性。在三种不同的细胞系(即恶性HepG2肝癌细胞)中研究了丁子香酚和冰片的细胞毒性及其DNA损伤作用及其对细胞对H(2)O(2)的DNA损伤作用的敏感性的影响。恶性Caco-2结肠细胞和非恶性人VH10成纤维细胞。锥虫蓝排除试验表明,在三种细胞系中,丁香酚的细胞毒性显着高于冰片。单细胞凝胶电泳显示,冰片在所研究的浓度下不会引起任何DNA链断裂,但显示丁香酚的所有浓度(<600 microM)都显着增加了人VH10成纤维细胞中DNA断裂的水平,并降低了水平。 Caco-2结肠细胞。在具有代谢活性的HepG2肝癌细胞中未观察到丁子香酚的DNA破坏作用。冰片和丁子香酚的DNA保护作用也不同。冰片可以保护HepG2,并在较小程度上保护VH10细胞(而不是Caco-2)抵抗H(2)O(2)诱导的DNA损伤,丁子香酚也不会对H(2)O(2)改变细胞敏感性)(HepG2细胞)或什至提高了敏感性(Caco-2和VH10细胞)。这些结果表明丁子香酚和冰片的DNA保护性和抗氧化能力之间没有任何关联。

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