硒甲基硒半胱氨酸对大鼠组织抗氧化系统的影响

Ho-Sang Shin, E. Choi
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引用次数: 0

摘要

我们评估了硒甲基硒代半胱氨酸(MSC)治疗对Sprague-Dawley大鼠组织抗氧化系统活性的影响,剂量为0.75 mg/大鼠/天,持续1或2周。谷胱甘肽和抗氧化酶活性在不同组织中有不同的变化。肝、肺和肾的谷胱甘肽含量及其还原状态在MSC治疗后升高,而脾脏的谷胱甘肽含量显著降低。在谷胱甘肽增加的组织中,有不同的酶反应:肝脏中谷胱甘肽合成途径的限制性酶g-谷氨酰半胱氨酸连接酶活性增加,而与谷胱甘肽再循环相关的酶,即谷胱甘肽过氧化物酶、谷胱甘肽还原酶和葡萄糖6-磷酸脱氢酶活性在肺和肾脏中显著增加。MSC处理后,各组织超氧化物歧化酶活性均降低,过氧化氢酶活性均升高,但肝脏除外。肺和肾的脂质过氧化水平在1周时短暂升高,而脾的脂质过氧化水平持续升高。这种增加在肝脏中并不明显。结果表明,间充质干细胞治疗导致肝、肺和肾的抗氧化能力增加,主要是通过增加谷胱甘肽含量和减少,这似乎是通过对间充质干细胞引发的氧化应激的组织依赖性适应性反应增加谷胱甘肽的合成或再循环的结果。脾脏对氧化应激非常敏感,因此,适应性反应不能提供抗氧化损伤的保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Se-methylselenocysteine on the Antioxidant System in Rat Tissues
We assessed the effect of Se-methylselenocysteine (MSC) treatment, at a dose of 0.75 mg/rat/day for 1 or 2 weeks, on the activities of antioxidant systems in Sprague-Dawley rat tissues. Significant changes in glutathione and antioxidant enzyme activities, with different patterns among tissues, were evidenced. Glutathione content and its reduction state in the liver, lung, and kidney were elevated upon MSC treatment, whereas they were significantly lowered in the spleen. Among the tissues exhibiting glutathione increase, there were different enzymatic responses: g-glutamylcysteine ligase activity, the rate-limiting enzyme in the glutathione synthesis pathway, was increased in the liver, whereas the activities of the enzymes associated with glutathione recycling, namely, glutathione peroxidase, glutathione reductase, and glucose 6-phosphate dehydrogenase, were significantly increased in the lung and the kidney. The superoxide dismutase activity was decreased in all tissues upon MSC treatment, whereas catalase activity was increased in all tissues but the liver. Lipid peroxidation level was transiently increased at 1 week in the lung and the kidney, whereas it was persistently increased in the spleen. The increase was not evident in the liver. The results indicate that the MSC treatment results in an increase in the antioxidant capacity of the liver, lung, and kidney principally via an increase in glutathione content and reduction, which appeared to be a result of increased synthesis or recycling of glutathione via tissue-dependent adaptive response to oxidative stress triggered by MSC. The spleen appeared to be very sensitive to oxidative stress, and therefore, the adaptive response could not provide protection against oxidative damage.
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