Yu Jisun, Kim An Keun
College Pharmacy, Sookmyung Women's University, Seoul, Korea.
Adv Exp Med Biol. 2009;643:491-9. doi: 10.1007/978-0-387-75681-3_51.
There is now increasing evidence that free radicals and reactive oxygen species (ROS) are involved in a variety of pathological events. Reactive oxygen species are produced during normal cellular function and lead to lipid peroxidation, massive protein oxidation and degradation. Taurine is an abundant free amino acid in inflammatory cells, where it is thought to be cytoprotective. The aim of the present study was to examine whether taurine enhances endogenous antioxidant enzyme activity and/or regulates ROS generation in B16F10 mouse melanoma cells. B16F10 cells were exposed to medium containing taurine for a period of 24 h. Cell viability, measured by the MTT assay, exhibited a dose-dose dependent inhibition. Taurine increased the activities of superoxide dismutase, glutathione peroxidase and CAT compared to those of the control, an effect paralleling an increase in gene expression. Taurine also reduced ROS content in a dose-dependent manner. Taken together, our results suggest that taurine decreases ROS levels by increasing the levels of the antioxidant enzymes.
现在越来越多的证据表明,自由基和活性氧(ROS)参与了多种病理过程。活性氧在正常细胞功能过程中产生,并导致脂质过氧化、大量蛋白质氧化和降解。牛磺酸是炎症细胞中一种丰富的游离氨基酸,被认为具有细胞保护作用。本研究的目的是检测牛磺酸是否能增强B16F10小鼠黑色素瘤细胞内源性抗氧化酶活性和/或调节活性氧的产生。将B16F10细胞暴露于含有牛磺酸的培养基中24小时。通过MTT法测定细胞活力,结果显示出剂量依赖性抑制。与对照组相比,牛磺酸增加了超氧化物歧化酶、谷胱甘肽过氧化物酶和CAT的活性,这一效应与基因表达的增加相平行。牛磺酸还以剂量依赖的方式降低了活性氧含量。综上所述,我们的结果表明,牛磺酸通过增加抗氧化酶水平来降低活性氧水平。