School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.
School of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.
Biomed Pharmacother. 2022 Jun;150:112982. doi: 10.1016/j.biopha.2022.112982. Epub 2022 Apr 26.
Anaphylaxis is a severe systemic allergic reaction that exhibits multiple clinical symptoms. The Mas-related G protein-coupled receptor X2 (MRGPRX2) is recognized as a key cell receptor mediating allergic diseases and drug-induced anaphylactoid reactions. Thus, it has been a promising target for preventing and treating these reactions. Based on the potential activity of imperatorin and active structural feature of MRGPRX2, we first demonstrated that the synthetic imperatorin derivatives (IDs) could significantly inhibit MRGPRX2 agonist-induced degranulation and cytokine release in LAD2 cells, as well as alleviate local and systemic anaphylaxis in mice. The IC value of the most promising compound is an order of magnitude lower than that of imperatorin. IDs were further identified to display anti-pseudo-allergic activity by binding MRGPRX2 with the tertiary nitrogen substructures, just liking the reported MRGPRX2-ligand. These results would propose evidence for discovery of agents for treating MCs-dependent allergic disorders.
过敏反应是一种严重的全身性过敏反应,表现出多种临床症状。Mas 相关 G 蛋白偶联受体 X2(MRGPRX2)被认为是介导过敏疾病和药物诱导的类过敏反应的关键细胞受体。因此,它已成为预防和治疗这些反应的有前途的靶点。基于白芷素的潜在活性和 MRGPRX2 的活性结构特征,我们首先证明了合成的白芷素衍生物(IDs)可以显著抑制 LAD2 细胞中 MRGPRX2 激动剂诱导的脱颗粒和细胞因子释放,并减轻小鼠的局部和全身过敏反应。最有前途的化合物的 IC 值比白芷素低一个数量级。IDs 进一步被鉴定为通过与三级氮亚结构结合 MRGPRX2 来显示抗假过敏活性,就像报道的 MRGPRX2 配体一样。这些结果为发现治疗 MC 依赖性过敏疾病的药物提供了依据。