杨梅减轻异丙苯氢过氧化物诱导的瑞士白化病小鼠皮肤氧化应激和毒性。

A Alam, M Iqbal, M Saleem, S Ahmed, S Sultana
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引用次数: 13

摘要

近年来,已经作出了相当大的努力,以确定可能对人类有用的新的化学预防剂。杨梅是一种亚热带灌木,已被证明具有显著的抗肝毒性和其他药理和生理疾病的活性。我们已经证明了杨梅对异丙苯氢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。30 mg/只/0.2 ml丙酮剂量水平的异丙苯氢过氧化物处理提高了皮肤微粒体膜对铁抗坏血酸诱导的脂质过氧化和黄嘌呤氧化酶活性的敏感性,并伴有皮肤过氧化氢酶、谷胱甘肽过氧化物酶、谷胱甘肽还原酶、葡萄糖-6-磷酸脱氢酶活性的降低和皮肤谷胱甘肽水平的降低。与这些变化平行的是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(30 mg/只动物/0.2 ml丙酮)治疗之前,分别用2.0 mg和4.0 mg/kg体重剂量的杨梅在丙酮中应用,可显著抑制异丙苯过氧化氢引起的皮肤氧化应激和毒性,且呈剂量依赖性。抗坏血酸铁诱导皮肤微粒体膜对脂质过氧化的敏感性增强,黄嘌呤氧化酶活性显著降低(P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myrica nagi attenuates cumene hydroperoxide-induced cutaneous oxidative stress and toxicity in Swiss albino mice.

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.

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