Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Shenzhen University Medical School, Shenzhen University, No. 1066 Xueyuan Road, Nanshan District, Shenzhen 518055, China.
Molecules. 2023 Jul 7;28(13):5271. doi: 10.3390/molecules28135271.
Formononetin (FNT) is a plant-derived isoflavone natural product with anti-inflammatory, antioxidant, and anti-allergic properties. We showed previously that FNT inhibits immunoglobulin E (IgE)-dependent mast cell (MC) activation, but the effect of FNT on IgE-independent MC activation is yet unknown. Our aim was to investigate the effects and possible mechanisms of action of FNT on IgE-independent MC activation and pseudoallergic inflammation. We studied the effects of FNT on MC degranulation in vitro with a cell culture model using compound C48/80 to stimulate either mouse bone marrow-derived mast cells (BMMCs) or RBL-2H3 cells. We subsequently measured β-hexosaminase and histamine release, the expression of inflammatory factors, cell morphological changes, and changes in NF-κB signaling. We also studied the effects of FNT in several in vivo murine models of allergic reaction: C48/80-mediated passive cutaneous anaphylaxis (PCA), active systemic anaphylaxis (ASA), and 2,4-dinitrobenzene (DNCB)-induced atopic dermatitis (AD). The results showed that FNT inhibited IgE-independent degranulation of MCs, evaluated by a decrease in the release of β-hexosaminase and histamine and a decreased expression of inflammatory factors. Additionally, FNT reduced cytomorphological elongation and F-actin reorganization and attenuated NF-κB p65 phosphorylation and NF-κB-dependent promoter activity. Moreover, the administration of FNT alleviated pseudoallergic responses in vivo in mouse models of C48/80-stimulated PCA and ASA, and DNCB-induced AD. In conclusion, we suggest that FNT may be a novel anti-allergic drug with great potential to alleviate pseudoallergic responses via the inhibition of IgE-independent MC degranulation and NF-κB signaling.
芒柄花素(FNT)是一种具有抗炎、抗氧化和抗过敏特性的植物衍生异黄酮天然产物。我们之前曾表明,FNT 可抑制免疫球蛋白 E(IgE)依赖性肥大细胞(MC)激活,但 FNT 对 IgE 非依赖性 MC 激活的影响尚不清楚。我们的目的是研究 FNT 对 IgE 非依赖性 MC 激活和假过敏炎症的作用及其可能的作用机制。我们使用化合物 C48/80 刺激体外细胞培养模型,研究了 FNT 对 MC 脱颗粒的影响,该模型使用了来自小鼠骨髓的肥大细胞(BMMC)或 RBL-2H3 细胞。随后,我们测量了β-己糖胺酶和组氨酸的释放、炎症因子的表达、细胞形态变化以及 NF-κB 信号的变化。我们还研究了 FNT 在几种过敏反应的体内小鼠模型中的作用:C48/80 介导的被动皮肤过敏反应(PCA)、主动全身性过敏反应(ASA)和 2,4-二硝基苯(DNCB)诱导的特应性皮炎(AD)。结果表明,FNT 通过降低β-己糖胺酶和组氨酸的释放以及降低炎症因子的表达,抑制了 IgE 非依赖性 MC 的脱颗粒。此外,FNT 减少了细胞形态的伸长和 F-肌动蛋白的重组,并减弱了 NF-κB p65 磷酸化和 NF-κB 依赖性启动子活性。此外,FNT 可减轻体内 C48/80 刺激 PCA 和 ASA 以及 DNCB 诱导 AD 的小鼠模型中的假过敏反应。总之,我们认为 FNT 可能是一种新型的抗过敏药物,通过抑制 IgE 非依赖性 MC 脱颗粒和 NF-κB 信号传导,具有缓解假过敏反应的巨大潜力。