Varela-Nallar Lorena, Arredondo Sebastian B, Tapia-Rojas Cheril, Hancke Juan, Inestrosa Nibaldo C
Centro de Investigaciones Biomédicas (CIB), Facultad de Ciencias Biológicas y Facultad de Medicina, Universidad Andrés Bello, Santiago, Chile.
Centro de Envejecimiento y Regeneración (CARE), Departamento de Biología Celular y Molecular, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Neural Plast. 2015;2015:935403. doi: 10.1155/2015/935403. Epub 2015 Dec 22.
Andrographolide (ANDRO) is a labdane diterpenoid component of Andrographis paniculata widely used for its anti-inflammatory properties. We have recently determined that ANDRO is a competitive inhibitor of glycogen synthase kinase-3β (GSK-3β), a key enzyme of the Wnt/β-catenin signaling cascade. Since this signaling pathway regulates neurogenesis in the adult hippocampus, we evaluated whether ANDRO stimulates this process. Treatment with ANDRO increased neural progenitor cell proliferation and the number of immature neurons in the hippocampus of 2- and 10-month-old mice compared to age-matched control mice. Moreover, ANDRO stimulated neurogenesis increasing the number of newborn dentate granule neurons. Also, the effect of ANDRO was evaluated in the APPswe/PS1ΔE9 transgenic mouse model of Alzheimer's disease. In these mice, ANDRO increased cell proliferation and the density of immature neurons in the dentate gyrus. Concomitantly with the increase in neurogenesis, ANDRO induced the activation of the Wnt signaling pathway in the hippocampus of wild-type and APPswe/PS1ΔE9 mice determined by increased levels of β-catenin, the inactive form of GSK-3β, and NeuroD1, a Wnt target gene involved in neurogenesis. Our findings indicate that ANDRO stimulates neurogenesis in the adult hippocampus suggesting that this drug could be used as a therapy in diseases in which neurogenesis is affected.
穿心莲内酯(ANDRO)是穿心莲中的一种贝壳杉烷二萜类成分,因其抗炎特性而被广泛应用。我们最近确定ANDRO是糖原合酶激酶-3β(GSK-3β)的竞争性抑制剂,GSK-3β是Wnt/β-连环蛋白信号级联反应的关键酶。由于该信号通路调节成年海马体中的神经发生,我们评估了ANDRO是否能刺激这一过程。与年龄匹配的对照小鼠相比,用ANDRO处理可增加2个月和10个月大的小鼠海马体中神经祖细胞的增殖以及未成熟神经元的数量。此外,ANDRO刺激神经发生,增加新生齿状颗粒神经元的数量。同时,在阿尔茨海默病的APPswe/PS1ΔE9转基因小鼠模型中评估了ANDRO的作用。在这些小鼠中,ANDRO增加了齿状回中细胞的增殖和未成熟神经元的密度。伴随着神经发生的增加,ANDRO通过增加β-连环蛋白、GSK-3β的无活性形式以及NeuroD1(一种参与神经发生的Wnt靶基因)的水平,诱导野生型和APPswe/PS1ΔE9小鼠海马体中Wnt信号通路的激活。我们的研究结果表明,ANDRO刺激成年海马体中的神经发生,提示该药物可用于治疗神经发生受影响的疾病。