首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Inhibitory effect of dihydroartemisinin against phorbol ester-induced cyclooxygenase-2 expression in macrophages
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Inhibitory effect of dihydroartemisinin against phorbol ester-induced cyclooxygenase-2 expression in macrophages

机译:双氢青蒿素对佛波酯诱导的巨噬细胞环氧合酶-2表达的抑制作用

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摘要

Dihydroartemisinin (DHA), a semi-synthetic derivative of artemisinin isolated from the traditional Chinese herb Artemisia annua L., has recently been shown to possess antitumor activity in various cancer cells. However, the effect of anti-inflammatory potentials of DHA in murine macrophage RAW 264.7 cells has not been studied. The present study investigated the effect of COX-2 and molecular mechanisms by DHA in PMA stimulated RAW 264.7 cells. DHA dose-dependently decreased PMA-induced COX-2 expression and PGE2 production, as well as COX-2 promoter-driven luciferase activity. Additionally, DHA decreased luciferase activity of COX-2 regulation-related transcription factors including NF-κB, AP-1, C/EBP and CREB. DHA also remarkably reduced PMA-induced p65, C/EBPβ, c-jun and CREB nuclear translocation. Furthermore, DHA evidently inhibited PMA-induced phosphorylation of AKT and the MAP Kinases, such as ERK, JNK and p38. Taken together, our data indicated that DHA effectively attenuates COX-2 production via down-regulation of AKT and MAPK pathway, revealing partial molecular basis for the anti-inflammatory properties of DHA.
机译:二氢青蒿素(DHA)是从传统中草药青蒿(Artemisia annua L.)分离出来的青蒿素的半合成衍生物,最近被证明在多种癌细胞中都具有抗肿瘤活性。但是,尚未研究DHA在小鼠巨噬细胞RAW 264.7细胞中的抗炎潜力。本研究调查了DHA对PMA刺激的RAW 264.7细胞产生COX-2的作用及其分子机制。 DHA剂量依赖性降低PMA诱导的COX-2表达和PGE2产生,以及COX-2启动子驱动的萤光素酶活性。此外,DHA降低了COX-2调节相关转录因子(包括NF-κB,AP-1,C / EBP和CREB)的萤光素酶活性。 DHA还显着降低了PMA诱导的p65,C /EBPβ,c-jun和CREB核易位。此外,DHA明显抑制了PMA诱导的AKT和MAP激酶(如ERK,JNK和p38)的磷酸化。两者合计,我们的数据表明DHA通过下调AKT和MAPK途径有效地减弱了COX-2的产生,揭示了DHA抗炎特性的部分分子基础。

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