Suppr超能文献

山茶花油的抗炎活性。

Anti-inflammatory activity of Camellia japonica oil.

作者信息

Kim Seungbeom, Jung Eunsun, Shin Seungwoo, Kim Moohan, Kim Young-Soo, Lee Jongsung, Park Deokhoon

机构信息

Biospectrum Life Science Institute, Seongnam, Korea.

出版信息

BMB Rep. 2012 Mar;45(3):177-82. doi: 10.5483/BMBRep.2012.45.3.177.

Abstract

Camellia japonica oil (CJ oil) has been used traditionally in East Asia to nourish and soothe the skin as well as help restore the elasticity of skin. CJ oil has also been used on all types of bleeding instances. However, little is known about its anti-inflammatory effects. Therefore, the anti-inflammatory effects of CJ oil and its mechanisms of action were investigated. CJ oil inhibited LPS-induced production of NO, PGE(2), and TNF-α in RAW264.7 cells. In addition, expression of COX-2 and iNOS genes was reduced. To evaluate the mechanism of the anti-inflammatory activity of CJ oil, LPS-induced activation of AP-1 and NF-κB promoters was found to be significantly reduced by CJ oil. LPS-induced phosphorylation of IκBα, ERK, p38, and JNK was also attenuated. Our results indicate that CJ oil exerts anti-inflammatory effects by downregulating the expression of iNOS and COX-2 genes through inhibition of NF-κB and AP-1 signaling. [BMB reports 2012; 45(3): 177-182].

摘要

山茶油(CJ油)在东亚地区传统上一直被用于滋养和舒缓肌肤,以及帮助恢复皮肤弹性。CJ油也被用于各类出血情况。然而,其抗炎作用却鲜为人知。因此,对CJ油的抗炎作用及其作用机制进行了研究。CJ油可抑制RAW264.7细胞中脂多糖(LPS)诱导的一氧化氮(NO)、前列腺素E2(PGE2)和肿瘤坏死因子-α(TNF-α)的产生。此外,环氧化酶-2(COX-2)和诱导型一氧化氮合酶(iNOS)基因的表达也有所降低。为评估CJ油抗炎活性的机制,发现CJ油可显著降低LPS诱导的活化蛋白-1(AP-1)和核因子-κB(NF-κB)启动子的活性。LPS诱导的IκBα、细胞外信号调节激酶(ERK)、p38和应激活化蛋白激酶(JNK)的磷酸化也有所减弱。我们的结果表明,CJ油通过抑制NF-κB和AP-1信号传导来下调iNOS和COX-2基因的表达,从而发挥抗炎作用。[《BMB报告》2012年;45(3): 177-182]

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