State Key Laboratory of Biomembrane and Membrane Biotechnology, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Brain Res. 2013 Apr 19;1506:35-43. doi: 10.1016/j.brainres.2013.02.026. Epub 2013 Feb 27.
Huperzine A (Hup A) is a lycopodium alkaloid from Huperzia serrata, which has been used as a therapeutic agent in several neurological disorders. Despite the diverse pharmacological activities Hup A has, its role in hippocampal neurogenesis remains to be established. This study showed that Hup A not only promoted the proliferation of cultured mouse embryonic hippocampal neural stem cells (NSCs), but also increased the newly generated cells in the subgranular zone (SGZ) of the hippocampus in adult mice. Furthermore, the in vitro findings indicated that low concentrations of Hup A stimulated the proliferation of cultured NSCs, whereas extremely high concentration of it decreased the cell proliferation. Hup A activated mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) signaling pathway, which was a well-known regulator of biological processes including cell proliferation and differentiation. ERK inhibitor dramatically inhibited the proliferative effect of Hup A on NSCs. Administration of Hup A to adult mice significantly enhanced the cell proliferation in dentate gyrus of hippocampus, and increased the remaining newborn cells 4 weeks after the drug administration. Moreover, the newly generated BrdU(+)/NeuN(+) neurons were also increased by Hup A treatment. These findings suggest a novel role of Hup A in neurogenesis and provide a new insight into its therapeutic effects in neurological disorders via a neurogenesis-related mechanism.
石杉碱甲(Hup A)是石杉属植物中的一种裂环烯醚萜类生物碱,已被用于多种神经退行性疾病的治疗。尽管 Hup A 具有多种药理学活性,但它在海马神经发生中的作用仍有待确定。本研究表明,Hup A 不仅促进了培养的小鼠胚胎海马神经干细胞(NSC)的增殖,而且增加了成年小鼠海马颗粒下区(SGZ)中新生成的细胞。此外,体外研究结果表明,低浓度的 Hup A 刺激了培养的 NSC 的增殖,而极高浓度的 Hup A 则降低了细胞增殖。Hup A 激活了丝裂原活化蛋白激酶/细胞外信号调节激酶(MAPK/ERK)信号通路,该通路是调节细胞增殖和分化等生物过程的重要信号通路。ERK 抑制剂显著抑制了 Hup A 对 NSC 的增殖作用。给予成年小鼠 Hup A 可显著增强海马齿状回的细胞增殖,并在给药 4 周后增加剩余的新生细胞。此外,Hup A 处理还增加了新生成的 BrdU(+) / NeuN(+)神经元的数量。这些发现提示 Hup A 在神经发生中具有新的作用,并为其通过神经发生相关机制在神经退行性疾病中的治疗作用提供了新的见解。