首页> 外文期刊>Redox Report >Inhibitory effect of 18-glycyrrhetinic acid on 12-O-tetradecanoyl phorbol-13-acetate-induced cutaneous oxidative stress and tumor promotion in mice
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Inhibitory effect of 18-glycyrrhetinic acid on 12-O-tetradecanoyl phorbol-13-acetate-induced cutaneous oxidative stress and tumor promotion in mice

机译:18-甘草次酸对小鼠12-O-十四烷酰phorbol-13-乙酸盐诱导的皮肤氧化应激的抑制作用及促进肿瘤的作用

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摘要

Glycyrrhetinic acid is an aglycone of glycyrrhizic acid, another major active component of licorice roots. Licorice root extract has been used for a long time as a medicine and a natural sweetening additive. In the present study, we found that glycyrrhetinic acid inhibits 12-O-tetradecanoylphorbol-13-acetate (TPA) mediated oxidative stress and tumor promotion in murine skin. Topical application of TPA alone in mouse skin enhances ornithine decarboxylase activity and also increases [3H]-thymidine incorporation in DNA. Topical application of TPA also resulted in the depletion of glutathione, activities of glutathione metabolizing and antioxidant enzymes. Application of glycyrrhetinic acid prior to TPA treatment reduces this enhanced ODC activity, [3H]-thymidine incorporation in DNA and oxidative stress. Glycyrrhetinic acid was also found to inhibit DMBA/TPA-induced skin tumor formation at doses of 1.25 and 2.5 mg by reducing the number of tumors per mouse by 24% (P < 0.05) and 62% (P < 0.05), respectively. These results suggest that glycyrrhetinic acid, an antioxidant, is a potential chemopreventive agent that can inhibit DMBA/TPA-induced cutaneous oxidative stress and tumor promotion.
机译:甘草次酸是甘草酸的糖苷配基,甘草根的另一主要活性成分。欧亚甘草根提取物已长期用作药物和天然甜味添加剂。在本研究中,我们发现甘草次酸抑制了鼠皮肤中12-O-十四烷酰phorbol-13-乙酸盐(TPA)介导的氧化应激和肿瘤的促进。单独在小鼠皮肤中局部施用TPA可以增强鸟氨酸脱羧酶活性,并且还可以增加[ 3 H]-胸腺嘧啶脱氧核苷在DNA中的掺入。 TPA的局部应用还导致谷胱甘肽的消耗,谷胱甘肽的代谢活性和抗氧化酶。在TPA处理之前施用甘草次酸可降低这种增强的ODC活性,DNA中的[ 3 H]-胸苷掺入和氧化应激。还发现甘草次酸通过将每只小鼠的肿瘤数分别减少24%(P <0.05)和62%(P <0.05)来抑制DMBA / TPA诱导的皮肤肿瘤形成。这些结果表明,甘草次酸,一种抗氧化剂,是一种潜在的化学预防剂,可以抑制DMBA / TPA诱导的皮肤氧化应激并促进肿瘤。

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  • 来源
    《Redox Report》 |2005年第3期|151-157|共7页
  • 作者单位

    Department of Medical Elementology and Toxicology, Faculty of Science, Jamia Hamdard (Hamdard University), New Delhi, India;

    Department of Medical Elementology and Toxicology, Faculty of Science, Jamia Hamdard (Hamdard University), New Delhi, India;

    Department of Medical Elementology and Toxicology, Faculty of Science, Jamia Hamdard (Hamdard University), New Delhi, India;

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