Ye Zhong, Mishchuk Darya O, Stephens Natasha S, Slupsky Carolyn M
Department of Nutrition, University of California, Davis, One Shields Avenue, Davis, CA 95616, USA; E-Mail:
Int J Mol Sci. 2011;12(4):2325-35. doi: 10.3390/ijms12042325. Epub 2011 Apr 4.
To understand and characterize the pathogenic mechanisms of inflammatory bowel disease, dextran sulfate sodium (DSS) has been used to induce acute and chronic colitis in animal models by causing intestinal epithelium damage. The mechanism of action of DSS in producing this outcome is not well understood. In an effort to understand how DSS might impact epithelial cell metabolism, we studied the intestinal epithelial cell line Caco-2 incubated with 1% DSS over 56 hours using (1)H NMR spectroscopy. We observed no difference in cell viability as compared to control cultures, and an approximately 1.5-fold increase in IL-6 production upon incubation with 1% DSS. The effect on Caco-2 cell metabolism as measured through changes in the concentration of metabolites in the cell supernatant included a three-fold decrease in the concentration of alanine. Given that the concentrations of other amino acids in the cell culture supernatant were not different between treated and control cultures over 56 hours suggest that DSS inhibits alanine synthesis, specifically alanine aminotransferase, without affecting other key metabolic pathways. The importance of alanine aminotransferase in inflammatory bowel disease is discussed.
为了理解和描述炎症性肠病的致病机制,硫酸葡聚糖钠(DSS)已被用于通过造成肠上皮损伤在动物模型中诱导急性和慢性结肠炎。DSS产生这种结果的作用机制尚不清楚。为了了解DSS如何影响上皮细胞代谢,我们使用¹H NMR光谱研究了在56小时内用1% DSS孵育的肠上皮细胞系Caco-2。与对照培养物相比,我们观察到细胞活力没有差异,并且在与1% DSS孵育后IL-6产生增加了约1.5倍。通过细胞上清液中代谢物浓度变化来衡量,对Caco-2细胞代谢的影响包括丙氨酸浓度下降了三倍。鉴于在56小时内处理组和对照组细胞培养上清液中其他氨基酸的浓度没有差异,这表明DSS抑制丙氨酸合成,特别是丙氨酸转氨酶,而不影响其他关键代谢途径。本文讨论了丙氨酸转氨酶在炎症性肠病中的重要性。