Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Key Laboratory of Fermentation Engineering (Ministry of Education), National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, 430068, Wuhan, China.
South Hubei Industrial Technology Research Institute for Characteristic Agriculture, 437100, Xianning, China.
Plant Foods Hum Nutr. 2022 Sep;77(3):405-411. doi: 10.1007/s11130-022-00988-x. Epub 2022 Jul 7.
Existing studies on the biological activity of theabrownins are not based on their free state but on the complexes of theabrownins, polysaccharides, proteins, and flavonoids. In this study, theabrownins (TBs-C) were prepared by weak alkali oxidation of tea polyphenols. The ultraviolet-visible scanning spectrum of TBs-C showed two characteristic absorption peaks at 203 and 270 nm. The zeta potential of the TBs-C aqueous solution was negative, and the values varied from - 6.26 to -19.55 mV with a solution pH of 3-9. Storage conditions of pH 5.0-7.0 and around 25 °C were beneficial for the physical and chemical stability of the TBS-C solution. Cells were treated with series concentrations and examined by MTT, HE staining, PI immunofluorescence staining, flow cytometry, and real-time PCR to investigate the antiproliferative effect of TBs-C on human colon cancer HT-29 cells. The results showed that TBs-C, particularly at 500 µg/mL, inhibited cell growth. TBs-C induced HT-29 cell apoptosis, as confirmed by morphological changes, nucleus propidium iodide staining, and distributions of the cell cycle. The apoptotic mechanism may be due to the intracellular redox imbalance induced by TBs-C.
现有关于茶褐素生物活性的研究不是基于其游离状态,而是基于茶褐素与多糖、蛋白质和类黄酮的复合物。本研究通过茶多酚弱碱氧化制备茶褐素(TBs-C)。TBs-C 的紫外-可见扫描光谱在 203 和 270nm 处显示出两个特征吸收峰。TBs-C 水溶液的 ζ 电位为负,溶液 pH 值为 3-9 时,其值从-6.26 到-19.55mV 变化。pH 5.0-7.0 和 25°C 左右的储存条件有利于 TBs-C 溶液的物理和化学稳定性。通过 MTT、HE 染色、PI 免疫荧光染色、流式细胞术和实时 PCR 检测系列浓度处理的细胞,研究 TBs-C 对人结肠癌 HT-29 细胞的增殖抑制作用。结果表明,TBs-C 特别是在 500μg/mL 时抑制细胞生长。TBs-C 诱导 HT-29 细胞凋亡,这通过形态变化、碘化丙啶核染色和细胞周期分布得到证实。凋亡机制可能是由于 TBs-C 引起的细胞内氧化还原失衡。