Department of Integrative Biotechnology, Sungkyunkwan University, Suwon 16419, Korea.
Biomedical Institute for Convergence at SKKU (BICS), Sungkyunkwan University, Suwon 16419, Korea.
Int J Mol Sci. 2022 Apr 3;23(7):3986. doi: 10.3390/ijms23073986.
Loratadine is an anti-histamine routinely used for treating allergies. However, recent findings have shown that Loratadine may also have anti-inflammatory functions, while their exact mechanisms have not yet been fully uncovered. In this paper, we investigated whether Loratadine can be utilized as an anti-inflammatory drug through a series of in vitro and in vivo experiments using a murine macrophage cell line and an acute gastritis mouse model. Loratadine was found to dramatically reduce the expression of pro-inflammatory genes, including MMP1, MMP3, and MMP9, and inhibit AP-1 transcriptional activation, as demonstrated by the luciferase assay. Therefore, we decided to further explore its role in the AP-1 signaling pathway. The expression of c-Jun and c-Fos, AP-1 subunits, was repressed by Loratadine and, correspondingly, the expression of p-JNK, p-MKK7, and p-TAK1 was also inhibited. In addition, Loratadine was able to reduce gastric bleeding in acute gastritis-induced mice; Western blotting using the stomach samples showed reduced p-c-Fos protein levels. Loratadine was shown to effectively suppress inflammation by specifically targeting TAK1 and suppressing consequent AP-1 signaling pathway activation and inflammatory cytokine production.
氯雷他定是一种常用于治疗过敏的抗组胺药。然而,最近的研究结果表明,氯雷他定可能还具有抗炎作用,但其确切机制尚未完全揭示。在本文中,我们通过一系列使用鼠巨噬细胞系和急性胃炎小鼠模型的体外和体内实验,研究了氯雷他定是否可以作为一种抗炎药物。荧光素酶检测表明,氯雷他定可显著降低促炎基因 MMP1、MMP3 和 MMP9 的表达,并抑制 AP-1 转录激活。因此,我们决定进一步探索其在 AP-1 信号通路中的作用。氯雷他定抑制 AP-1 亚基 c-Jun 和 c-Fos 的表达,相应地,抑制 p-JNK、p-MKK7 和 p-TAK1 的表达。此外,氯雷他定能够减少急性胃炎诱导的小鼠胃出血;胃组织样本的 Western blot 分析显示 p-c-Fos 蛋白水平降低。氯雷他定通过特异性靶向 TAK1 并抑制随后的 AP-1 信号通路激活和炎症细胞因子的产生,有效地抑制炎症。