Chang Sai, Ruan Wen-Chen, Xu Ya-Zhou, Wang Yun-Jie, Pang Jie, Zhang Lu-Yong, Liao Hong, Pang Tao
Jiangsu Key Laboratory of Drug Screening, State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China.
Jiangsu Key Laboratory of Drug Discovery for Metabolic Diseases, China Pharmaceutical University, Nanjing 210009, China.
Acta Pharmacol Sin. 2017 Jan;38(1):29-40. doi: 10.1038/aps.2016.115. Epub 2016 Nov 14.
Recent studies focus on promoting neurite outgrowth to remodel the central nervous network after brain injury. Currently, however, there are few drugs treating brain diseases in the clinic by enhancing neurite outgrowth. In this study, we established an NGF-induced PC12 differentiation model to screen novel compounds that have the potential to induce neuronal differentiation, and further characterized 4,10-Aromadendranediol (ARDD) isolated from the dried twigs of the Baccharis gaudichaudiana plant, which exhibited the capability of promoting neurite outgrowth in neuronal cells in vitro. ARDD (1, 10 μmol/L) significantly enhanced neurite outgrowth in NGF-treated PC12 cells and N1E115 cells in a time-dependent manner. In cultured primary cortical neurons, ARDD (5, 10 μmol/L) not only significantly increased neurite outgrowth but also increased the number of neurites on the soma and the number of bifurcations. Further analyses showed that ARDD (10 μmol/L) significantly increased the phosphorylation of ERK1/2 and the downstream GSK-3β, subsequently induced β-catenin expression and up-regulated the gene expression of the Wnt ligands Fzd1 and Wnt3a in neuronal cells. The neurite outgrowth-promoting effect of ARDD in neuronal cells was abolished by pretreatment with the specific ERK1/2 inhibitor PD98059, but was partially reversed by XAV939, an inhibitor of the Wnt/β-catenin pathway. ARDD also increased the expression of BDNF, CREB and GAP-43 in N1E115 cells, which was reversed by pretreatment with PD98059. In N1E115 cells subjected to oxygen and glucose deprivation (OGD), pretreatment with ARDD (1-10 μmol/L) significantly enhanced the phosphorylation of ERK1/2 and induced neurite outgrowth. These results demonstrated that the natural product ARDD exhibits neurite outgrowth-inducing activity in neurons via activation of the ERK signaling pathway, which may be beneficial to the treatment of brain diseases.
最近的研究集中在促进神经突生长以在脑损伤后重塑中枢神经网络。然而,目前临床上通过增强神经突生长来治疗脑部疾病的药物很少。在本研究中,我们建立了神经生长因子(NGF)诱导的PC12分化模型,以筛选具有诱导神经元分化潜力的新型化合物,并进一步对从高氏酒神菊植物干燥嫩枝中分离出的4,10-芳樟二醇(ARDD)进行了表征,该化合物在体外神经元细胞中表现出促进神经突生长的能力。ARDD(1、10 μmol/L)以时间依赖性方式显著增强了NGF处理的PC12细胞和N1E115细胞中的神经突生长。在原代培养的皮质神经元中,ARDD(5、10 μmol/L)不仅显著增加了神经突生长,还增加了胞体上的神经突数量和分支数量。进一步分析表明,ARDD(10 μmol/L)显著增加了细胞外信号调节激酶1/2(ERK1/2)和下游糖原合成酶激酶-3β(GSK-3β)的磷酸化,随后诱导β-连环蛋白表达,并上调神经元细胞中Wnt配体Fzd1和Wnt3a的基因表达。用特异性ERK1/2抑制剂PD98059预处理可消除ARDD在神经元细胞中的神经突生长促进作用,但Wnt/β-连环蛋白通路抑制剂XAV939可部分逆转该作用。ARDD还增加了N1E115细胞中脑源性神经营养因子(BDNF)、环磷腺苷效应元件结合蛋白(CREB)和生长相关蛋白43(GAP-43)的表达,用PD98059预处理可使其逆转。在经历氧糖剥夺(OGD)的N1E115细胞中,用ARDD(1-10 μmol/L)预处理显著增强了ERK1/2的磷酸化并诱导了神经突生长。这些结果表明,天然产物ARDD通过激活ERK信号通路在神经元中表现出神经突生长诱导活性,这可能对脑部疾病的治疗有益。