Department of Chemical and Pharmaceutical Engineering, College of Chemical Engineering, Huaqiao University, Xiamen, 361021, Fujian province, PR China.
Xiamen Medicine Research Institute, Xiamen, 361008, Fujian province, PR China.
J Ethnopharmacol. 2021 Jun 28;274:114046. doi: 10.1016/j.jep.2021.114046. Epub 2021 Mar 20.
Ethnopharmacological relevance Paeonia lactiflora is a famous Traditional Chinese medicine widely used for immunological regulation. Paeoniflorin, the main component of Paeonia lactiflora, exerts neuroprotective and antidepressant-like effects in rodents.
Fibroblast growth factor 2 (FGF-2) is essentially required in the central nervous system as it acts as both a neurotrophic factor and an anti-inflammatory factor participating in the regulation of proliferation, differentiation and apoptosis of neurons in the brain. However, it is unclear whether paeoniflorin could exert antidepressant effects via regulating FGF-2.
In the present study, the effects of paeoniflorin were evaluated in depressive mice induced by the endotoxin lipopolysaccharide (LPS) injection.
The results showed that paeoniflorin markedly increased sucrose preference and reduced immobility time in LPS mice, indicating antidepressant effects. Consistent with the results from molecular docking showing paeoniflorin antagonizes TLR4, NF-κB and NLRP3, the biochemical analysis also indicated paeoniflorin inhibited TLR4/NF-κB/NLRP3 signaling, decreased proinflammatory cytokine levels and microglial activation in the hippocampus of LPS induced mice. In addition, the levels of neuronal FGF-2 and the density of dendritic spine were improved by paeoniflorin. More importantly, the FGFR1 inhibitor SU5402 prevented the antidepressant effects of paeoniflorin and blocked the neuroinflammatory and neurogenic regulatory effects of paeoniflorin, indicating that FGF-2/FGFR1 activation was required for the effects of paeoniflorin.
Taken together, the results demonstrate that paeoniflorin exhibits neuroprotective and antidepressant effects in mice, which may be mediated by activating neuronal FGF-2/FGFR1 signaling via the inhibition of microglial activation in the hippocampus.
白芍是一种著名的中药,广泛用于免疫调节。芍药苷是白芍的主要成分,在啮齿类动物中具有神经保护和抗抑郁样作用。
成纤维细胞生长因子 2 (FGF-2) 是中枢神经系统中必不可少的物质,因为它既是神经营养因子,也是抗炎因子,参与调节大脑中神经元的增殖、分化和凋亡。然而,芍药苷是否可以通过调节 FGF-2 发挥抗抑郁作用尚不清楚。
本研究评估了芍药苷在脂多糖 (LPS) 注射诱导的抑郁小鼠中的作用。
结果表明,芍药苷显著增加 LPS 小鼠的蔗糖偏好,减少不动时间,表明具有抗抑郁作用。与分子对接结果一致,表明芍药苷拮抗 TLR4、NF-κB 和 NLRP3,生化分析还表明芍药苷抑制 TLR4/NF-κB/NLRP3 信号通路,降低 LPS 诱导的小鼠海马促炎细胞因子水平和小胶质细胞激活。此外,芍药苷还改善了神经元 FGF-2 水平和树突棘密度。更重要的是,FGFR1 抑制剂 SU5402 可预防芍药苷的抗抑郁作用,并阻断芍药苷的神经炎症和神经发生调节作用,表明 FGF-2/FGFR1 激活是芍药苷作用所必需的。
综上所述,研究结果表明,芍药苷在小鼠中表现出神经保护和抗抑郁作用,这可能是通过抑制海马中小胶质细胞的激活来激活神经元 FGF-2/FGFR1 信号通路介导的。