刘继勇, 赵永哲, 彭程, 李凤前, 朱全刚, 胡晋红. 盐酸西替利嗪对表皮角质形成细胞和真皮成纤维细胞P物质受体和细胞因子表达的影响J. 药学学报, 2008, 43(4): 383-387.
引用本文: 刘继勇, 赵永哲, 彭程, 李凤前, 朱全刚, 胡晋红. 盐酸西替利嗪对表皮角质形成细胞和真皮成纤维细胞P物质受体和细胞因子表达的影响J. 药学学报, 2008, 43(4): 383-387.
LIU Ji-yong, ZHAO Yong-zhe, PENG Cheng, LI Feng-qian, ZHU Quan-gang, HU Jin-hong. Effect of cetirizine hydrochloride on the expression of substance P receptor and cytokines production in human epidermal keratinocytes and dermal fibroblastsJ. Acta Pharmaceutica Sinica, 2008, 43(4): 383-387.
Citation: LIU Ji-yong, ZHAO Yong-zhe, PENG Cheng, LI Feng-qian, ZHU Quan-gang, HU Jin-hong. Effect of cetirizine hydrochloride on the expression of substance P receptor and cytokines production in human epidermal keratinocytes and dermal fibroblastsJ. Acta Pharmaceutica Sinica, 2008, 43(4): 383-387.

盐酸西替利嗪对表皮角质形成细胞和真皮成纤维细胞P物质受体和细胞因子表达的影响

Effect of cetirizine hydrochloride on the expression of substance P receptor and cytokines production in human epidermal keratinocytes and dermal fibroblasts

  • 摘要: 研究抗组胺药盐酸西替利嗪对表皮角质形成细胞系HaCaT细胞和真皮成纤维细胞P物质受体表达以及对P物质诱导两种细胞表达IFN-γ、IL-1β、IL-6及IL-8的影响。采用流式细胞术和Western blotting检测分析西替利嗪对两种皮肤细胞P物质受体表达的影响;以P物质刺激HaCaT细胞和真皮成纤维细胞,加入不同剂量的西替利嗪共孵育,采用ELISA方法测定西替利嗪对IFN-γ、IL-1β、IL-6及IL-8分泌的影响。结果表明,西替利嗪显著抑制HaCaT细胞和真皮成纤维细胞P物质受体的表达;P物质刺激可以显著增加HaCaT细胞和真皮成纤维细胞IFN-γ、IL-1β、IL-8的分泌量;1~100 μmol·L-1的西替利嗪均可抑制皮肤细胞IL-1β、IL-8的分泌,但对IFN-γ的分泌无明显影响。P物质和西替利嗪对两种皮肤细胞IL-6的产生均无显著影响。

     

    Abstract: To investigate the effect of cetirizine hydrochloride on the expression of neurokinin 1 receptor (NK-1R) and cytokines production induced by substance P (SP) in HaCaT cells (a human epidermal keratinocyte cell line) and dermal fibroblasts. The effect of cetirizine on the expression of NK-1R protein was detected by flow cytometry and Western blotting analysis. The modulation of cetirizine on the production of interferon (IFN)-γ, interleukin (IL)-1β, IL-6 and IL-8 in HaCaT cells and fibroblasts was measured by ELISA. The results showed that cetirizine significantly inhibited the expression of NK-1R in HaCaT cells and fibroblasts. SP induced the production of IFN-γ, IL-1β and IL-8 in both cell types. Cetirizine 1-100 μmol·L-1 inhibited SP-induced IL-1β and IL-8 production in HaCaT cells and fibroblasts, while had no effect on the production of IFN-γ in both cells. Both SP and cetirizine had no effect on the secretion of IL-6 in HaCaT cells and fibroblasts. These findings suggest that cetirizine may be involved in the treatment of SP-induced skin inflammation by inhibiting the expression of substance P receptor and regulation the production of IL-1β and IL-8 in epidermal keratinocyte and dermal fibroblasts.

     

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