Suppr超能文献

黄芩素通过雌激素受体和 NF-κB 依赖性途径在 LPS 刺激的 RAW264.7 巨噬细胞中发挥抗炎作用。

Anti-inflammatory activity of baicalein in LPS-stimulated RAW264.7 macrophages via estrogen receptor and NF-κB-dependent pathways.

机构信息

State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 300193, China.

出版信息

Inflammation. 2013 Dec;36(6):1584-91. doi: 10.1007/s10753-013-9703-2.

Abstract

Baicalein has been used for many years as a popular antiviral and antibacterial in China. Recent investigations revealed that baicalein also has anti-inflammatory activities. Our results indicated that baicalein increases ERE-luciferase activity in an estrogen receptor (ER)-dependent manner when either ERα or ERβ were coexpressed in Hela cells. This study examined whether baicalein exerts an anti-inflammatory effect in RAW264.7 cells through an estrogen receptor-dependent pathway and through regulation of NF-ĸB activation. In lipopolysaccharide (LPS)-induced RAW264.7 cells, baicalein exerts anti-inflammatory effects by inhibiting iNOS, COX-2, and TNF-α mRNA expression; NO production; as well as inflammatory cytokine (IL-1β, PGE2, and TNF-α) production through an ER-dependent pathway. These effects are accompanied with the inhibition of the transcription factor NF-ĸB activation and IκBα phosphorylation. We therefore conclude that baicalein inhibits LPS-induced inflammatory cytokine production via regulation of the NF-ĸB pathway and estrogen-like activity, suggesting that it may be useful for preventing inflammation-related diseases.

摘要

黄芩素在中国已被用作一种流行的抗病毒和抗菌药物多年。最近的研究表明,黄芩素还具有抗炎活性。我们的结果表明,黄芩素在 Hela 细胞中同时表达 ERα或 ERβ时,以雌激素受体(ER)依赖性方式增加 ERE-荧光素酶活性。本研究通过雌激素受体依赖性途径和 NF-ĸB 激活的调节,研究了黄芩素是否通过雌激素受体依赖性途径在 RAW264.7 细胞中发挥抗炎作用。在脂多糖(LPS)诱导的 RAW264.7 细胞中,黄芩素通过抑制 iNOS、COX-2 和 TNF-α mRNA 表达、NO 产生以及炎症细胞因子(IL-1β、PGE2 和 TNF-α)的产生来发挥抗炎作用。这些作用伴随着转录因子 NF-ĸB 激活和 IκBα磷酸化的抑制。因此,我们得出结论,黄芩素通过调节 NF-ĸB 途径和雌激素样活性抑制 LPS 诱导的炎症细胞因子产生,表明它可能有助于预防与炎症相关的疾病。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验