首页> 外文期刊>Pharmacology and Toxicology: An International Journal >Myrica nagi attenuates cumene hydroperoxide-induced cutaneous oxidative stress and toxicity in Swiss albino mice.
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Myrica nagi attenuates cumene hydroperoxide-induced cutaneous oxidative stress and toxicity in Swiss albino mice.

机译:杨梅(Myrica nagi)减轻了瑞士白化病小鼠中异丙苯过氧化氢诱导的皮肤氧化应激和毒性。

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In recent years, considerable efforts have been made to identify new chemopreventive agents which could be useful for man. Myrica nagi, a subtropical shrub, has been shown to possess significant activity against hepatotoxicity and other pharmacological and physiological disorders. We have shown a chemopreventive effect of Myrica nagi on cumene hydroperoxide-induced cutaneous oxidative stress and toxicity in mice. Cumene hydroperoxide treatment at a dose level of 30 mg/animal/0.2 ml acetone enhances susceptibility of cutaneous microsomal membrane for iron-ascorbate-induced lipid peroxidation and induction of xanthine oxidase activity which are accompanied by decrease in the activities of cutaneous antioxidant enzymes such as catalase, glutathione peroxidase, glutathione reductase, glucose-6-phosphate dehydrogenase and depletion in the level of cutaneous glutathione. Parallel to these changes a sharp decrease in the activities of phase II metabolizing enzymes such as glutathione S-transferase and quinone reductase has been observed. Application of Myrica nagi at doses of 2.0 mg and 4.0 mg/kg body weight in acetone prior to that of cumene hydroperoxide (30 mg/animal/0.2 ml acetone) treatment resulted in significant inhibition of cumene hydroperoxide-induced cutaneous oxidative stress and toxicity in a dose-dependent manner. Enhanced susceptibility of cutaneous microsomal membrane for lipid peroxidation induced by iron ascorbate and xanthine oxidase activities were significantly reduced (P<0.05). In addition the depleted level of glutathione, the inhibited activities of antioxidants, and phase II metabolizing enzymes were recovered to a significant level (P<0.05). The protective effect of Myrica nagi was dose-dependent. In summary our data suggest that Myrica nagi is an effective chemopreventive agent in skin and capable of ameliorating cumene hydroperoxide-induced cutaneous oxidative stress and toxicity.
机译:近年来,已经做出了巨大的努力来确定对人类有用的新的化学预防剂。洋紫苏,一种亚热带灌木,已显示出对肝毒性和其他药理和生理疾病具有显着活性。我们已经显示了杨梅(Myrica nagi)对异丙苯异丙基苯过氧化物诱导的小鼠皮肤氧化应激和毒性的化学预防作用。异丙苯以30 mg /动物/0.2 ml丙酮的剂量处理过氧化氢会增强皮肤微粒体膜对抗坏血酸铁引起的脂质过氧化和黄嘌呤氧化酶活性的敏感性,并伴随着皮肤抗氧化酶活性的降低,例如过氧化氢酶,谷胱甘肽过氧化物酶,谷胱甘肽还原酶,6-磷酸葡萄糖脱氢酶和皮肤谷胱甘肽水平的降低。与这些变化平行,已经观察到II期代谢酶如谷胱甘肽S-转移酶和醌还原酶的活性急剧下降。在异丙苯过氧化氢异丙苯(30 mg /动物/0.2 ml丙酮)处理之前,在丙酮中以2.0 mg和4.0 mg / kg体重的剂量施用Myrica nagi可以显着抑制异丙苯过氧化氢诱导的皮肤氧化应激和毒性。剂量依赖性的方式。皮肤微粒体膜对抗坏血酸铁引起的脂质过氧化和黄嘌呤氧化酶活性的敏感性增强(P <0.05)。此外,谷胱甘肽的消耗水平,抗氧化剂的抑制活性和II期代谢酶也被恢复到显着水平(P <0.05)。杨梅的保护作用是剂量依赖性的。总而言之,我们的数据表明,杨梅是一种有效的皮肤化学预防剂,能够改善异丙苯过氧化氢诱导的皮肤氧化应激和毒性。

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