Liu Xu, Wang Dongxiao, Zhao Runqing, Dong Xianzhe, Hu Yuan, Liu Ping
Department of Clinical Pharmacology and Pharmacy, Pharmacy Care Center, Chinese PLA General Hospital Beijing, China.
Front Pharmacol. 2016 Sep 27;7:337. doi: 10.3389/fphar.2016.00337. eCollection 2016.
As two natural oligosaccharide esters, 3,6'-Disinapoyl sucrose (DISS) and tenuifolisideA (TFSA) are originating from the root of Willd, a traditional Chinese medicine used in treatment of mental disorders. Previous reports have shown that both of them possess neuroprotective effects by stimulating different upstream pathways related with cyclic AMP-responsive element-binding protein (CREB). In the present study, we investigated the additive neuroprotective effects of DISS and TFSA on Glu-induced damage of SY5Y cells and purposed the possible underlying mechanism. The interaction between DISS and TFSA showed a clear-cut synergistic effect as evidenced by combination index (CI). Additional evidence from biochemical (NOS activity) assays confirmed their additive inhibition on the Glu-induced NOS hyperactivation. Moreover, we showed that co-treatment of DISS and TFSA resulted in an additively up-regulated phosphorylation of CREB as well as increased expressions of CRTC1 and BDNF. Neuroprotective effects of DISS and TFSA on Glu-induced decrease in cell viability were blocked by MAPK/ERK1/2 inhibitor (U0126) and PI3-K inhibitor (LY290042). Nevertheless, the CRTC1 or BDNF expression induced by these two compounds was significantly reduced in the presence of either ERK or PI3-K inhibitor, indicating that the two oligosaccharide esters shared some common pathways in the regulation of CREB-BDNF pathway. Taken together, we, for the first time, showed that DISS and TFSA exerted the additive neuroprotective effects on CREB-BDNF signaling pathway through complementary mechanisms.
作为两种天然低聚糖酯,3,6'-二芥子酰蔗糖(DISS)和细叶远志苷A(TFSA)源自远志,一种用于治疗精神障碍的传统中药。先前的报道表明,它们两者都通过刺激与环磷酸腺苷反应元件结合蛋白(CREB)相关的不同上游途径而具有神经保护作用。在本研究中,我们研究了DISS和TFSA对谷氨酸(Glu)诱导的SY5Y细胞损伤的相加神经保护作用,并探讨了可能的潜在机制。DISS和TFSA之间的相互作用表现出明显的协同效应,联合指数(CI)证明了这一点。来自生化(一氧化氮合酶活性)测定的额外证据证实了它们对Glu诱导的一氧化氮合酶过度激活的相加抑制作用。此外,我们表明,DISS和TFSA共同处理导致CREB的磷酸化相加上调以及CRTC1和脑源性神经营养因子(BDNF)的表达增加。DISS和TFSA对Glu诱导的细胞活力下降的神经保护作用被丝裂原活化蛋白激酶/细胞外信号调节激酶1/2(MAPK/ERK1/2)抑制剂(U0126)和磷脂酰肌醇-3激酶(PI3-K)抑制剂(LY294002)阻断。然而,在存在ERK或PI3-K抑制剂的情况下,这两种化合物诱导的CRTC1或BDNF表达显著降低,表明这两种低聚糖酯在CREB-BDNF途径的调节中共享一些共同途径。综上所述,我们首次表明,DISS和TFSA通过互补机制对CREB-BDNF信号通路发挥相加神经保护作用。