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Diminution of free radical induced DNA damage by extracts/fractions from bark of Schleichera oleosa (Lour.) Oken

机译:鞘脂schleichera oleosa(Lour。)Oken的树皮提取物/馏分减少自由基诱导的DNA损伤

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The present study was undertaken to investigate the effect of extracts of Schleichera oleosa (Sapindaceae) for its cytotoxic and hydroxyl radical-scavenging activities. The bark of the tree was used to prepare extracts with different solvents (i.e., hexane, chloroform, ethyl acetate, methanol, and water). The extracts were initially assessed for their in vitro cytotoxicity potential in the sulforhodamine B dye assay against cell lines, such as 502713 (colon), SW-620 (colon), HCT-15 (colon), A-549 (lung), HEP-2 (liver), SK-NS-H (central nervous system), and IMR-32 (neuroblastoma). It was observed that the water extract was effective against all the three colon cancer cell lines, while only methanol and water extracts were effective against A-549 (lung) and HEP-2 (liver), respectively. As DNA damage is one of the hallmarks of cell death, so the extracts were assessed for their ability to scavenge hydroxyl radicals, in the deoxyribose degradation assay (site- and nonsite specific) as well as their protective effect against the hydroxyl radical-induced DNA damage in the plasmid nicking assay, using pBR322. It was observed that all the extracts, except chloroform and hexane, exhibited relatively greater antioxidant activity in the nonsite-specific than in the site-specific assay. Similarly, the extracts were also found to be effective in inhibiting the hydroxyl radical-induced unwinding of supercoiled DNA, which further confirmed the hydroxyl radical-scavenging ability of the extracts in the deoxyribose degradation method.
机译:进行本研究以研究油茶schleichera oleosa(Sapindaceae)提取物的细胞毒性和清除羟自由基的作用。树皮被用来制备具有不同溶剂(即己烷,氯仿,乙酸乙酯,甲醇和水)的提取物。最初在磺基罗丹明B染料分析中评估了提取物对细胞系(例如502713(冒号),SW-620(冒号),HCT-15(冒号),A-549(肺),HEP)的体外细胞毒性潜力-2(肝脏),SK-NS-H(中枢神经系统)和IMR-32(神经母细胞瘤)。观察到水提取物对所有三种结肠癌细胞系均有效,而仅甲醇和水提取物分别对A-549(肺)和HEP-2(肝)有效。由于DNA损伤是细胞死亡的标志之一,因此在脱氧核糖降解试验(位点和非位点特异性)中评估了提取物清除羟自由基的能力以及对羟自由基诱导的DNA的保护作用。使用pBR322在质粒切口分析中发现损伤。观察到,除氯仿和己烷外,所有提取物在非位点特异性检测中均显示出比位点特异性检测法相对更高的抗氧化活性。类似地,还发现提取物可有效抑制羟自由基诱导的超螺旋DNA的解旋,这进一步证实了在脱氧核糖降解方法中提取物的羟自由基清除能力。

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