Department of Molecular Pharmacology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8505, Japan.
Department of Pharmacognosy, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8505, Japan.
J Med Invest. 2020;67(3.4):289-297. doi: 10.2152/jmi.67.289.
As the expression level of allergic disease sensitive genes are correlated with the severity of allergic symptoms, suppression of these gene expressions could be promising therapeutics. We demonstrated that protein kinase Cδ / heat shock protein 90-mediated H1R gene expression signaling and nuclear factor of activated T-cells (NFAT)-mediated IL-9 gene expression signaling are responsible for the pathogenesis of pollinosis. Treatment with Awa-tea combined with wild grape hot water extract suppressed these signaling and alleviated nasal symptoms in toluene-2,4-diisocyanate (TDI)-sensitized rats. However, the underlying mechanism of its anti-allergic activity is not elucidated yet. Here, we sought to identify an anti-allergic compound from Awa-tea and pyrogallol was identified as an active compound. Pyrogallol strongly suppressed ionomycin-induced up-regulation of IL-9 gene expression in RBL-2H3 cells. Treatment with pyrogallol in combination with epinastine alleviated nasal symptoms and suppressed up-regulation of IL-9 gene expression in TDI-sensitized rats. Pyrogallol itself did not inhibit calcineurin phosphatase activity. However, pyrogallol suppressed ionomycin-induced dephosphorylation and nuclear translocation of NFAT. These data suggest pyrogallol is an anti-allergic compound in Awa-tea and it suppressed NFAT-mediated IL-9 gene expression through the inhibition of dephosphorylation of NFAT. This might be the underlying mechanism of the therapeutic effects of combined therapy of pyrogallol with antihistamine. J. Med. Invest. 67 : 289-297, August, 2020.
由于过敏疾病敏感基因的表达水平与过敏症状的严重程度相关,因此抑制这些基因的表达可能是一种有前途的治疗方法。我们证明蛋白激酶 Cδ/热休克蛋白 90 介导的 H1R 基因表达信号和激活的 T 细胞核因子 (NFAT) 介导的 IL-9 基因表达信号负责花粉病的发病机制。用 Awa 茶联合野生葡萄热水提取物治疗可抑制这些信号,并缓解甲苯二异氰酸酯 (TDI) 致敏大鼠的鼻症状。然而,其抗过敏活性的潜在机制尚未阐明。在这里,我们试图从 Awa 茶中鉴定出一种抗过敏化合物,发现焦倍酚是一种活性化合物。焦倍酚强烈抑制 RBL-2H3 细胞中离子霉素诱导的 IL-9 基因表达上调。焦倍酚与依帕司他联合治疗可缓解 TDI 致敏大鼠的鼻症状,并抑制 IL-9 基因表达的上调。焦倍酚本身不能抑制钙调神经磷酸酶活性。然而,焦倍酚抑制了离子霉素诱导的 NFAT 去磷酸化和核转位。这些数据表明,焦倍酚是 Awa 茶中的一种抗过敏化合物,它通过抑制 NFAT 的去磷酸化来抑制 NFAT 介导的 IL-9 基因表达。这可能是焦倍酚与抗组胺药联合治疗的治疗效果的潜在机制。医学研究杂志 67:289-297,2020 年 8 月。