青藤碱
脂多糖
麦加明
肿瘤坏死因子α
化学
药理学
小干扰RNA
基因敲除
炎症
烟碱拮抗剂
受体
烟碱激动剂
免疫学
医学
生物化学
转染
基因
细胞凋亡
作者
Lang Yi,Jin-Fang Luo,Bing Xie,Jianxin Liu,Jun-yue Wang,Liang Liu,Peixun Wang,Hua Zhou,Yan Dong
出处
期刊:Shock
[Lippincott Williams & Wilkins]
日期:2015-04-18
卷期号:44 (2): 188-195
被引量:55
标识
DOI:10.1097/shk.0000000000000389
摘要
Sinomenine (SIN), an alkaloid derived from the plant Sinomenium acutum, has anti-inflammatory and analgesic effects and has been used for rheumatoid arthritis treatment in China. This study aims to verify the hypothesis that SIN acts on α7 nicotinic acetylcholine receptor (α7nAChR) to inhibit the activation of macrophages stimulated by lipopolysaccharide. The prototypical α7nAChR antagonist α-bungarotoxin and mecamylamine attenuated the effect of SIN on tumor necrosis factor-α and interleukin-6 in RAW264.7 murine macrophage-like cells and primary peritoneal macrophages of mouse induced by lipopolysaccharide. With the knockdown of α7nAChR expression in RAW264.7 cells by small interfering RNA, the inhibitory effect of SIN on tumor necrosis factor-α and interleukin-6 was reversed. Sinomenine decreased p65 expression in nuclear and increased IκBα expression in cytoplasm, and these effects were reversed by the α7nAChR small interfering RNA as well. These results indicate that the anti-inflammatory effects of SIN on macrophages in vitro depend on α7nAChR.
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