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Quantitative measurements of oxidative stress in mouse skin induced by X-ray irradiation

机译:X射线照射引起的小鼠皮肤氧化应激的定量测量

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摘要

To find efficient methods to evaluate oxidative stress in mouse skin caused by X-ray irradiation, several markers and methodologies were examined. Hairless mice were irradiated with 50 Gy X-rays and skin homogenates or skin strips were prepared. Lipid peroxidation was measured using the skin homogenate as the level of thiobarbituric acid reactive substances. The level of lipid peroxidation increased with time after irradiation and was twice that of the control at 78 h. ESR spectra of skin strips showed a clear signal for the ascorbyl radical, which increased with time after irradiation in a manner similar to that of lipid peroxidation. To measure levels of glutathione (GSH) and its oxidized forms (GSSG) simultaneously, two HPLC methods, sample derivatization with 1-fluoro-2,4-dinitrobenzene and detection with a UV detector (method A) and no derivatization and detection with an electrochemical detector (method B), were compared and the latter was found to be better. No significant change was observed within 24 h after irradiation in the levels of GSH and GSSG measured by method B. The GSH/GSSG ratio may be a less sensitive parameter for the evaluation of acute oxidative stress caused by X-ray irradiation in the skin. Monitoring the ascorbyl radical seems to be a good way to evaluate oxidative stress in skin in vivo.
机译:为了找到评估由X射线照射引起的小鼠皮肤氧化应激的有效方法,研究了几种标记物和方法。用50 Gy X射线照射无毛小鼠,制备皮肤匀浆或皮肤条。使用皮肤匀浆作为硫代巴比妥酸反应性物质的水平,测量脂质过氧化。辐照后脂质过氧化水平随时间增加,在78 h时是对照的两倍。皮肤条的ESR光谱显示出抗坏血酸基团的清晰信号,该信号在辐射后随时间增加,其方式类似于脂质过氧化作用。为了同时测量谷胱甘肽(GSH)和其氧化形式(GSSG)的水平,有两种HPLC方法:使用1-氟-2,4-二硝基苯进行样品衍生化和使用UV检测器进行检测(方法A),而无需进行衍生化和检测。比较了电化学检测器(方法B),发现后者更好。照射后24小时内,方法B测得的GSH和GSSG含量未见明显变化。GSH/ GSSG比可能不是评估皮肤X射线照射引起的急性氧化应激的敏感参数。监测抗坏血酸基团似乎是评估体内皮肤氧化应激的好方法。

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