Department of Strategic Surveillance for Functional Food and Comprehensive Traditional Medicine, Wakayama Medical University, 811-1 Kimiidera, Wakayama City, Wakayama, 641-0012, Japan.
Department of Applied Chemistry and Biochemistry, National Institute of Technology, Wakayama College, 77 Noshima, Nada, Gobo, Wakayama, 644-0023, Japan.
Eur J Pharmacol. 2020 Oct 15;885:173435. doi: 10.1016/j.ejphar.2020.173435. Epub 2020 Jul 31.
Zanthoxylum piperitum (ZP, 'Japanese pepper') is a traditional medicine and pepper used in Asian countries such as Japan. Hydroxy-α-sanshool, a pungent-tasting substance contained within ZP, has been reported to slightly suppress immunoglobulin E (IgE)-mediated mast cell degranulation. The current study aims to newly identify anti-allergic compounds derived from ZP. We examine the inhibitory mechanisms behind IgE-mediated mast cell degranulation. By inhibitory effect-guided isolation, we identified degranulation inhibitory compounds derived from ZP fruit: 1-acetoxy-7-hydroxy-3, 7-dimethylocta-2E, 5E-diene (ZP1) and 8-hydroxygeranyl acetate (ZP2). ZP1 and ZP2 inhibited IgE-mediated degranulation and A23187-mediated degranulation in RBL-2H3 mast cells. Our findings suggest the inhibition of degranulation by ZP1 and ZP2 was by inhibition of Lyn phosphorylation, followed by inhibition of intracellular Ca mobilization, protein kinase C alpha phosphorylation, membrane ruffling, and granule-to-plasma membrane fusion. Oral administration of ZP1 or ZP2 attenuated an IgE-mediated passive cutaneous anaphylactic reaction in mice. Histological observation suggests that this effect occurred via inhibition of mast cell degranulation. These findings indicate that ZP1 and ZP2 attenuate allergic reaction via inhibition of IgE-mediated mast cell degranulation.
花椒(ZP,“日本胡椒”)是一种传统药物和胡椒,在日本等亚洲国家使用。ZP 中含有的羟基-α-山椒素,已被报道可轻微抑制免疫球蛋白 E(IgE)介导的肥大细胞脱颗粒。本研究旨在从 ZP 中鉴定新的抗过敏化合物。我们研究了 IgE 介导的肥大细胞脱颗粒的抑制机制。通过抑制作用导向分离,我们从 ZP 果实中鉴定出了具有脱颗粒抑制作用的化合物:1-乙酰氧基-7-羟基-3,7-二甲基辛-2E,5E-二烯(ZP1)和 8-羟基香叶基乙酸酯(ZP2)。ZP1 和 ZP2 抑制 RBL-2H3 肥大细胞中 IgE 介导的脱颗粒和 A23187 介导的脱颗粒。我们的研究结果表明,ZP1 和 ZP2 通过抑制 Lyn 磷酸化,进而抑制细胞内 Ca2+动员、蛋白激酶 Cα 磷酸化、膜皱襞形成和颗粒与质膜融合,来抑制脱颗粒。ZP1 或 ZP2 的口服给药可减轻小鼠 IgE 介导的被动皮肤过敏反应。组织学观察表明,这种作用是通过抑制肥大细胞脱颗粒来实现的。这些发现表明,ZP1 和 ZP2 通过抑制 IgE 介导的肥大细胞脱颗粒来减轻过敏反应。