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首页> 外文期刊>Oxidative Medicine and Cellular Longevity >Proanthocyanidins Produce Significant Attenuation of Doxorubicin-Induced Mutagenicity via Suppression of Oxidative Stress
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Proanthocyanidins Produce Significant Attenuation of Doxorubicin-Induced Mutagenicity via Suppression of Oxidative Stress

机译:原花青素通过抑制氧化应激产生阿霉素诱导的致突变性显着降低。

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This study has been initiated to determine whether proanthocyanidins can protect against doxorubicin-induced mutagenicity in mice and to elucidate the potential mechanism of this protection. Pretreatment of mice with proanthocyanidins (100 mg/kg/day, orally) for 7 days and simultaneously with doxorubicin (12 mg/kg, i.p.) for another day, significantly reduced the frequency of bone marrow DNA strand breaks and micronucleated polychromatic erythrocytes compared to doxorubicin-treated mice alone. Furthermore, proanthocyanidins caused a reduction in bone marrow suppression induced by doxorubicin treatment. In male germline, orally administration of proanthocyanidins (100 mg/kg/day, orally) for 7 consecutive days before and 7 consecutive days after treatment with doxorubicin (12 mg/ kg, i.p.), significantly elevated the levels of sperm count and motility reduced by doxorubicin treatment. Furthermore, proanthocyanidins significantly decreased the elevated levels of spermatogonial and spermatocyte chromosomal aberrations and sperm head abnormality induced by doxorubicin. Prior administration of proanthocyanidins ahead of doxorubicin reduced the doxorubicin induced testicular lipid peroxidation and prevented the reduction in testicularnonprotein sulfhydryl significantly. Conclusively, this study provides for the first time that proanthocyanidins have a protective role in the abatement of doxorubicin-induced mutagenesis and cell proliferation changes in germinal cells of mice that reside, at least in part, in their radical scavengeractivity. Therefore, proanthocyanidins can be a promising chemopreventive agent to avert secondary malignancy and abnormal reproductive outcomes risks in cancer patients receiving doxorubicin-involved treatment.
机译:这项研究已经开始,以确定原花青素是否可以保护小鼠免受阿霉素诱导的致突变性,并阐明这种保护的潜在机制。与原花青素(100 mg / kg /天,口服)一起对小鼠进行预处理7天,同时与阿霉素(12 mg / kg,腹膜内)同时进行另一天的预处理,与之相比,显着降低了骨髓DNA链断裂和微核多色红细胞的频率单独使用阿霉素治疗的小鼠。此外,原花青素引起由阿霉素治疗引起的骨髓抑制的减少。在雄性种系中,在用阿霉素(12 mg / kg,ip)治疗之前连续7天和治疗后连续7天口服原花青素(100 mg / kg /天,口服),显着提高了精子数量水平,降低了运动能力通过阿霉素治疗。此外,原花青素显着降低了阿霉素引起的精原细胞和精细胞染色体畸变以及精子头部异常的升高水平。在阿霉素之前预先施用原花青素可降低阿霉素诱导的睾丸脂质过氧化作用,并显着阻止睾丸非蛋白巯基的减少。结论是,这项研究首次提供了原花青素在减轻阿霉素诱导的诱变和小鼠生发细胞中细胞增殖变化方面的保护作用,这些小鼠至少部分地存在于其自由基清除能力中。因此,原花青素可以成为有希望的化学预防剂,以防止接受阿霉素治疗的癌症患者继发恶性肿瘤和异常生殖结果风险。

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