Chen Bai Hui, Park Joon Ha, Cho Jeong Hwi, Kim In Hye, Lee Jae Chul, Lee Tae-Kyeong, Ahn Ji Hyeon, Tae Hyun Jin, Shin Bich Na, Kim Jong-Dai, Kang Il Jun, Won Moo-Ho, Lee Yun Lyul
Department of Physiology, Institute of Neurodegeneration and Neuroregeneration, College of Medicine, Hallym University, Chuncheon, 24252, South Korea.
Department of Neurobiology, School of Medicine, Kangwon National University, Chuncheon, 24341, South Korea.
Neurochem Res. 2016 Aug;41(8):1958-68. doi: 10.1007/s11064-016-1906-0. Epub 2016 Apr 6.
Tanshinone I (TsI), a lipophilic diterpene extracted from Danshan (Radix Salvia miltiorrhizae), exerts neuroprotection in cerebrovascular diseases including transient ischemic attack. In this study, we examined effects of TsI on cell proliferation and neuronal differentiation in the subgranular zone (SGZ) of the mouse dentate gyrus (DG) using Ki-67, BrdU and doublecortin (DCX) immunohistochemistry. Mice were treated with 1 and 2 mg/kg TsI for 28 days. In the 1 mg/kg TsI-treated-group, distribution patterns of BrdU, Ki-67 and DCX positive ((+)) cells in the SGZ were similar to those in the vehicle-treated-group. However, in the 2 mg/kg TsI-treated-group, double labeled BrdU(+)/NeuN(+) cells, which are mature neurons, as well as Ki-67(+), DCX(+) and BrdU(+) cells were significantly increased compared with those in the vehicle-treated-group. On the other hand, immunoreactivities and protein levels of Wnt-3, β-catenin and serine-9-glycogen synthase kinase-3β (p-GSK-3β), which are related with morphogenesis, were significantly increased in the granule cell layer of the DG only in the 2 mg/kg TsI-treated-group. Therefore, these findings indicate that TsI can promote neurogenesis in the mouse DG and that the neurogenesis is related with increases of Wnt-3, p-GSK-3β and β-catenin immunoreactivities.
丹参酮I(TsI)是从丹参(丹参根)中提取的一种亲脂性二萜,在包括短暂性脑缺血发作在内的脑血管疾病中发挥神经保护作用。在本研究中,我们使用Ki-67、BrdU和双皮质素(DCX)免疫组织化学方法,检测了TsI对小鼠齿状回(DG)颗粒下区(SGZ)细胞增殖和神经元分化的影响。小鼠接受1和2mg/kg的TsI治疗28天。在1mg/kg TsI治疗组中,SGZ中BrdU、Ki-67和DCX阳性((+))细胞的分布模式与载体治疗组相似。然而,在2mg/kg TsI治疗组中,与载体治疗组相比,成熟神经元双标记的BrdU(+)/NeuN(+)细胞以及Ki-67(+)、DCX(+)和BrdU(+)细胞显著增加。另一方面,仅在2mg/kg TsI治疗组中,DG颗粒细胞层中与形态发生相关的Wnt-3、β-连环蛋白和丝氨酸-9-糖原合酶激酶-3β(p-GSK-3β)的免疫反应性和蛋白水平显著增加。因此,这些发现表明TsI可以促进小鼠DG中的神经发生,并且神经发生与Wnt-3、p-GSK-3β和β-连环蛋白免疫反应性的增加有关。