Kim Seungbeom, Jung Eunsun, Shin Seungwoo, Kim Moohan, Kim Young-Soo, Lee Jongsung, Park Deokhoon
Biospectrum Life Science Institute, Seongnam, Korea.
BMB Rep. 2012 Mar;45(3):177-82. doi: 10.5483/BMBRep.2012.45.3.177.
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].
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]