Department of Anatomy and Neurobiology, and Institute of Neurodegeneration and Neuroregeneration, College of Medicine, Hallym University, Chuncheon 200-702, South Korea.
Phytother Res. 2010 Jul;24(7):1065-70. doi: 10.1002/ptr.3083.
Neurogenesis is regulated by several factors such as age, stress and pharmacological agents. We observed the effects of (-)-epigallocatechin-3-gallate (EGCG), a major catechin of green tea, on neurogenesis in mice. The animals were orally administered EGCG for 4 weeks. Brain sections were stained using a marker for cell proliferation (Ki67 and BrdU) and neuroblasts (doublecortin, DCX). In all groups, Ki67, BrdU and DCX immunoreaction were observed in the subgranular zone of the dentate gyrus. Oral administration of EGCG significantly increased the number of Ki67-, BrdU- and DCX-immunoreactive cells as well as BrdU/DCX-colabled cells in the subgranular zone when compared to those in the vehicle-treated group. These results indicate that oral administration of EGCG can enhance cell proliferation and increase the number of neuroblasts in mice hippocampal dentate gyrus.
神经发生受多种因素调节,如年龄、应激和药物等。我们观察了绿茶中主要儿茶素 (-)-表没食子儿茶素没食子酸酯 (EGCG) 对小鼠神经发生的影响。动物经口给予 EGCG 4 周。使用细胞增殖标志物 (Ki67 和 BrdU) 和神经前体细胞 (双皮质素,DCX) 对脑切片进行染色。在所有组中,均在齿状回颗粒下区观察到 Ki67、BrdU 和 DCX 免疫反应。与对照组相比,EGCG 口服给药可显著增加 Ki67、BrdU 和 DCX 免疫反应细胞以及 BrdU/DCX 标记细胞的数量。这些结果表明,EGCG 口服给药可增强细胞增殖并增加小鼠海马齿状回神经前体细胞的数量。