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首页> 外文期刊>Teratogenesis, carcinogenesis, and mutagenesis >Inhibitory effect of Eucommia ulmoides Oliv. on oxidative DNA damage in lymphocytes induced by H2O2.
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Inhibitory effect of Eucommia ulmoides Oliv. on oxidative DNA damage in lymphocytes induced by H2O2.

机译:杜仲对杜仲的抑制作用。对H2O2诱导的淋巴细胞氧化DNA损伤的影响。

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This study used the alkaline single cell gel electrophoresis assay (comet assay) to investigate the effect of water extracts of roasted cortex and leaves from Du-zhong on DNA damage in lymphocytes induced by H(2)O(2). The results showed that the DNA damage in human lymphocytes increased with an increase in the concentration of H(2)O(2) (0-200 micro;M), but that the water extracts from Du-zhong (0-2 g l(-1)) only slightly affected DNA damage. The inhibitory effect of leaf extract on DNA damage induced by H(2)O(2) in lymphocytes was more significant (P<0.05) than that of roasted cortex. Leaf extract showed a rather significant inhibitory effect in a concentration-dependent manner. At a concentration of 2 g l(-1), the leaf extract inhibited 37.9% DNA oxidative damage in human lymphocytes. In order to elucidate the mechanism of the leaf extract suppression effect on DNA damage induced by H(2)O(2) in lymphocytes, an experiment was divided with six groups (A-F). Group A was used to evaluate the repair ability of the leaf extract for DNA damage; Group B was employed to determine the scavenging ability on H(2)O(2); and Group C was studied to assess the ability of leaf extract to increase the defense capability. Groups D-F were negative controls and blank. The results showed that group B had the best inhibitory effect. Also, leaf extract had significant ability to scavenge H(2)O(2) in an in vitro HRP-phenol red test. Thus, it appears that H(2)O(2) scavenging potency may be the major mechanism whereby leaf extract inhibits oxidative DNA damage induced by H(2)O(2). Teratogenesis Carcinog. Mutagen. Suppl. 1:23-34, 2003. Copyright 2003 Wiley-Liss, Inc.
机译:这项研究使用碱性单细胞凝胶电泳测定法(彗星测定法)来研究杜仲的烤皮和叶的水提取物对H(2)O(2)诱导的淋巴细胞DNA损伤的影响。结果表明,人类淋巴细胞的DNA损伤随着H(2)O(2)(0-200 micro; M)浓度的增加而增加,但是水是从杜仲(0-2 gl( -1))仅轻微影响DNA损伤。叶提取物对H(2)O(2)诱导的淋巴细胞DNA损伤的抑制作用比烤皮层更显着(P <0.05)。叶提取物以浓度依赖性的方式显示出相当显着的抑制作用。在2 g l(-1)的浓度下,叶提取物可抑制人淋巴细胞中37.9%的DNA氧化损伤。为了阐明叶提取物抑制作用对淋巴细胞中H(2)O(2)诱导的DNA损伤的作用机理,将实验分为六组(A-F)。 A组用于评估叶片提取物对DNA损伤的修复能力。 B组用于确定对H(2)O(2)的清除能力;研究了C组,以评估叶提取物增强防御能力的能力。 D-F组为阴性对照,空白。结果表明,B组具有最佳的抑制作用。此外,叶提取物在体外HRP-酚红测试中具有清除H(2)O(2)的显着能力。因此,似乎H(2)O(2)清除能力可能是主要的机制,借此叶提取物抑制H(2)O(2)诱导的氧化DNA损伤。致癌作用。诱变剂。补充1:23-34,2003年。版权所有2003 Wiley-Liss,Inc.。

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