赵甜甜, 沈珑瑛, 潘显道. 白三烯B4受体拮抗剂的研究进展J. 药学学报, 2022, 57(10): 3133-3145. DOI: 10.16438/j.0513-4870.2022-0602
引用本文: 赵甜甜, 沈珑瑛, 潘显道. 白三烯B4受体拮抗剂的研究进展J. 药学学报, 2022, 57(10): 3133-3145. DOI: 10.16438/j.0513-4870.2022-0602
ZHAO Tian-tian, SHEN Long-ying, PAN Xian-dao. Research progress of leukotriene B4 receptor antagonistsJ. Acta Pharmaceutica Sinica, 2022, 57(10): 3133-3145. DOI: 10.16438/j.0513-4870.2022-0602
Citation: ZHAO Tian-tian, SHEN Long-ying, PAN Xian-dao. Research progress of leukotriene B4 receptor antagonistsJ. Acta Pharmaceutica Sinica, 2022, 57(10): 3133-3145. DOI: 10.16438/j.0513-4870.2022-0602

白三烯B4受体拮抗剂的研究进展

Research progress of leukotriene B4 receptor antagonists

  • 摘要: 白三烯B4 (leukotriene B4, LTB4) 是一种促炎调节因子, 多数炎症细胞均可产生。LTB4与其受体BLT1 (leukotriene B4 receptor 1) 结合后可通过趋化作用和黏附分子上调将嗜中性粒细胞和巨噬细胞迁移至炎症部位。大量研究表明LTB4-BLT1轴与自身免疫性疾病及炎症的发生有关。因此, LTB4受体拮抗剂对治疗这类疾病具有重要作用。本文简略描述了LTB4的作用, 综述了目前处于临床或临床前研究的LTB4受体拮抗剂的研究进展。

     

    Abstract: Leukotriene B4 (LTB4) is a proinflammatory lipid mediator that is synthesized by a number of inflammatory cells. Binding of LTB4 to its receptor leukotriene B4 receptor 1 (BLT1) can migrate neutrophils and macrophages to inflammatory sites through chemotaxis and up-regulation of adhesion molecules. Many researches have shown that LTB4-BLT1 axis is related to the occurrence of autoimmune disorders and other inflammatory diseases. Receptor antagonists of LTB4 are thus expected to be useful therapeutics for these diseases. In this review, we briefly describe the biological function of LTB4 and summarize the preclinical and clinical developments of LTB4 receptor antagonists.

     

/

返回文章
返回