Inhibitory effect of phellodendrine on C48/80-induced allergic reaction in vitro and in vivo

体内 体外 化学 抑制性突触后电位 药理学 生物 生物化学 神经科学 生物技术
作者
Jing Wang,Jianzeng Liu,Yang Yang,Guang Sun,Guang Sun,Dan Yang,Shuhe Yin,Shuai Zhang,Wenqi Jin,Daqing Zhao,Liwei Sun,Rui Jiang
出处
期刊:International Immunopharmacology [Elsevier BV]
卷期号:134: 112256-112256 被引量:12
标识
DOI:10.1016/j.intimp.2024.112256
摘要

The incidence of allergic reactions has risen steadily in recent years, prompting growing interest in the identification of efficacious and safe natural compounds that can prevent or treat allergic diseases. Phellodendron amurense Rupr. has long been applied as a treatment for allergic diseases, whose primary component is phellodendrine. However, the efficacy of phellodendrine as a treatment for allergic diseases remains to be assessed. Mast cells are the primary effectors of allergic reactions, which are not only activated by IgE-dependent pathway, but also by IgE-independent pathways via human MRGPRX2, rat counterpart MRGPRB3. As such, this study explored the effect and mechanism of phellodendrine through this family receptors in treating allergic diseases in vitro and in vivo. These analyses revealed that phellodendrine administration was sufficient to protect against C48/80-induced foot swelling and Evans blue exudation in mice, and suppressed C48/80-induced RBL-2H3 rat basophilic leukemia cells degranulation, and β-HEX, HIS, IL-4, and TNF-α release. Moreover, phellodendrine could reduce the mRNA expression of MRGPRB3 and responsiveness of MRGPRX2 by altering its structure. It was able to decrease Ca
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