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首页> 外文期刊>Life sciences >Effects of naringin on cytosine arabinoside (Ara-C)-induced cytotoxicity and apoptosis in P388 cells.
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Effects of naringin on cytosine arabinoside (Ara-C)-induced cytotoxicity and apoptosis in P388 cells.

机译:柚皮苷对阿糖胞苷(Ara-C)诱导的P388细胞毒性和凋亡的影响。

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摘要

Naringin (NG), a flavonoid in grapefruit and citrus, has been reported to exhibit antioxidant effects and pharmacological actions. Recently, we have reported that NG suppressed the cytotoxicity and apoptosis induced by H(2)O(2), a typical pro-oxidant, in mouse leukemia P388 cells. Cytosine arabinoside (1-beta-d-arabinofuranosylcytosine; Ara-C) is the most important antimetabolite chemotherapeutic drug used for acute leukemia. It has been suggested that Ara-C-induced cytotoxicity is caused by apoptosis, which is mediated by reactive oxygen species (ROS). In this study, we examined the effect of NG on the cytotoxicity and apoptosis in mouse leukemia P388 cells treated with Ara-C. Ara-C caused cytotoxicity in a concentration and time-dependent manner in the cells. N-Acetyl-L-cysteine (NAC), cystamine (CysA) or a reduced form of glutathione (GSH), typical antioxidants significantly blocked Ara-C-induced cytotoxicity. Similarly, Ara-C-induced cell death was completely prevented by NG. NG strongly reduced ROS production caused by Ara-C in the cells. NG slightly increased the activities of antioxidant enzymes, catalase and glutathione peroxidase. Ara-C caused apoptosis with nuclear morphological change and DNA fragmentation. NG remarkably attenuated the Ara-C-induced apoptosis. NG completely blocked the DNA damage caused by Ara-C treatment at 6 h using the Comet assay. Our data suggest that NG reduces Ara-C-induced oxidative stress through both an inhibition of the generation of ROS production and an increase in antioxidant enzyme activities. Consequently, NG blocked apoptosis caused by Ara-C-induced oxidative stress, resulting in the inhibition of the cytotoxicity of Ara-C.
机译:据报道柚皮和柑橘中的类黄酮柚皮素(NG)具有抗氧化作用和药理作用。最近,我们已经报道了NG抑制了小鼠白血病P388细胞中典型的促氧化剂H(2)O(2)诱导的细胞毒性和凋亡。胞嘧啶阿拉伯糖苷(1-β-d-阿拉伯呋喃糖基胞嘧啶; Ara-C)是用于急性白血病的最重要的抗代谢药物。已经提出,Ara-C诱导的细胞毒性是由凋亡引起的,凋亡是由活性氧(ROS)介导的。在这项研究中,我们检查了NG对Ara-C处理的小鼠白血病P388细胞的细胞毒性和凋亡的影响。 Ara-C在细胞中以浓度和时间依赖性方式引起细胞毒性。 N-乙酰基-L-半胱氨酸(NAC),胱胺(CysA)或还原型谷胱甘肽(GSH)是典型的抗氧化剂,可显着阻断Ara-C诱导的细胞毒性。类似地,NG完全防止了Ara-C诱导的细胞死亡。 NG强烈减少了细胞中由Ara-C引起的ROS产生。 NG略微增加了抗氧化酶,过氧化氢酶和谷胱甘肽过氧化物酶的活性。 Ara-C引起细胞凋亡,具有核形态变化和DNA片段化。 NG显着减弱了Ara-C诱导的细胞凋亡。 NG使用彗星分析法完全阻断了由Ara-C处理在6小时内引起的DNA损伤。我们的数据表明,NG可通过抑制ROS的产生和增加抗氧化酶的活性来降低Ara-C诱导的氧化应激。因此,NG阻断了由Ara-C诱导的氧化应激引起的细胞凋亡,从而抑制了Ara-C的细胞毒性。

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