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首页> 外文期刊>Oxidative Medicine and Cellular Longevity >Antigenotoxic and Apoptotic Activity of Green Tea Polyphenol Extracts on Hexavalent Chromium-Induced DNA Damage in Peripheral Blood of CD-1 Mice: Analysis with Differential Acridine Orange/Ethidium Bromide Staining
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Antigenotoxic and Apoptotic Activity of Green Tea Polyphenol Extracts on Hexavalent Chromium-Induced DNA Damage in Peripheral Blood of CD-1 Mice: Analysis with Differential Acridine Orange/Ethidium Bromide Staining

机译:绿茶多酚提取物对六价铬诱导的CD-1小鼠外周血DNA损伤的抗遗传毒性和凋亡活性:差示A啶橙/溴化乙锭染色分析

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This study was conducted to investigate the modulating effects of green tea polyphenols on genotoxic damage and apoptotic activity induced by hexavalent chromium [Cr (VI)] in CD-1 mice. Animals were divided into the following groups: (i) injected with vehicle; (ii) treated with green tea polyphenols (30 mg/kg) via gavage; (iii) injected with CrO3(20 mg/kg) intraperitoneally; (iv) treated with green tea polyphenols in addition to CrO3. Genotoxic damage was evaluated by examining micronucleated polychromatic erythrocytes (MN-PCEs) obtained from peripheral blood at 0, 24, 48, and 72 h after treatment. Induction of apoptosis and cell viability were assessed by differential acridine orange/ethidium bromide (AO/EB) staining. Treatment of green tea polyphenols led to no significant changes in the MN-PCEs. However, CrO3treatment significantly increased MN-PCEs at 24 and 48 h after injection. Green tea polyphenols treatment prior to CrO3injection led to a decrease in MN-PCEs compared to the group treated with CrO3only. The average of apoptotic cells was increased at 48 h after treatment compared to control mice, suggesting that apoptosis could contribute to eliminate the DNA damaged cells induced by Cr (VI). Our findings support the proposed protective effects of green tea polyphenols against the genotoxic damage induced by Cr (VI).
机译:进行这项研究以研究绿茶多酚对CD-1小鼠中六价铬[Cr(VI)]诱导的遗传毒性损伤和细胞凋亡活性的调节作用。将动物分为以下几组:(i)注射媒介物; (ii)通过管饲法用绿茶多酚(30毫克/千克)处理; (iii)腹腔注射CrO3(20 mg / kg); (iv)除CrO3外,还用绿茶多酚处理。通过检查在治疗后0、24、48和72 h从外周血获得的微核多色红细胞(MN-PCE)来评估遗传毒性损害。通过差异differential啶橙/溴化乙锭(AO / EB)染色评估凋亡的诱导和细胞活力。绿茶多酚的处理未导致MN-PCE发生明显变化。但是,CrO3处理在注射后24和48 h显着增加了MN-PCE。与仅用CrO3处理的组相比,在注射CrO3之前的绿茶多酚处理导致MN-PCE减少。与对照小鼠相比,在处理后48小时,凋亡细胞的平均值增加了,这表明细胞凋亡可能有助于消除由Cr(VI)诱导的DNA损伤的细胞。我们的发现支持拟议的绿茶多酚对Cr(VI)引起的遗传毒性损害的保护作用。

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