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奥佛酚对脂多糖处理的RAW 264.7细胞中一氧化氮生成及NF-κB/MAP激酶激活的抑制作用

Inhibitory effect of obovatol on nitric oxide production and activation of NF-kappaB/MAP kinases in lipopolysaccharide-treated RAW 264.7cells.

作者信息

Choi Myoung Suk, Lee Seung Ho, Cho Ho Seong, Kim Youngsoo, Yun Yeo Pyo, Jung Hai Young, Jung Jae Kyoung, Lee Bum Chun, Pyo Hyeong Bae, Hong Jin Tae

机构信息

College of Pharmacy, Chungbuk National University, 48, Gaesin-dong, Heungduk-gu, Cheongju, Chungbuk 361-763, South Korea.

出版信息

Eur J Pharmacol. 2007 Feb 5;556(1-3):181-9. doi: 10.1016/j.ejphar.2006.10.054. Epub 2006 Oct 28.

Abstract

The components of Magnolia obovata are known to have many pharmacological activities. In this study, we investigated the effects of obovatol, a neolignan compound isolated from the leaves of M. obovata, on nitric oxide (NO) production and NF-kappaB activity in lipopolysaccharide (LPS)-activated RAW 264.7 cells. The results show that obovatol (1-5 microM) significantly inhibited LPS-induced NO production in a concentration-dependent manner (IC(50): 0.91 microM). Consistent with the inhibitory effect on NO production, obovatol inhibits the expression of inducible nitric oxide synthase and cyclooxygenase-2 expression. Furthermore, obovatol suppressed NF-kappaB (p50 and p65) translocation to the nucleus as well as IkappaB release resulting in the inhibition of the DNA binding activity of the NF-kappaB. Obovatol also inhibited c-Jun N-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) signal, which are the most significantly involved signal in NO production and NF-kappaB activation. When the cells were treated with the combination of obovatol with U0126 (an ERK inhibitor) or SP600125 (a JNK inhibitor) as well as with SC-514 (an IKK2 inhibitor), much more inhibition of NO production was observed than that by obovatol alone. The present results suggest that obovatol has an inhibitory effect on NO production through the inhibition of NF-kappaB/MAPK activity, and thus can be used as an anti-inflammatory agent.

摘要

已知厚朴的成分具有多种药理活性。在本研究中,我们研究了从厚朴叶中分离出的一种新木脂素化合物——倒卵叶木兰脂素(obovatol)对脂多糖(LPS)激活的RAW 264.7细胞中一氧化氮(NO)生成和核因子κB(NF-κB)活性的影响。结果表明,倒卵叶木兰脂素(1-5微摩尔)以浓度依赖性方式显著抑制LPS诱导的NO生成(半数抑制浓度(IC50):0.91微摩尔)。与对NO生成的抑制作用一致,倒卵叶木兰脂素抑制诱导型一氧化氮合酶的表达和环氧合酶-2的表达。此外,倒卵叶木兰脂素抑制NF-κB(p50和p65)向细胞核的转位以及IκB的释放,从而抑制NF-κB的DNA结合活性。倒卵叶木兰脂素还抑制c-Jun氨基末端激酶(JNK)和细胞外信号调节激酶(ERK)信号,这是NO生成和NF-κB激活中最显著涉及的信号。当细胞用倒卵叶木兰脂素与U0126(一种ERK抑制剂)或SP600125(一种JNK抑制剂)以及SC-514(一种IKK2抑制剂)联合处理时,观察到对NO生成的抑制作用比单独使用倒卵叶木兰脂素更强。目前的结果表明,倒卵叶木兰脂素通过抑制NF-κB/丝裂原活化蛋白激酶(MAPK)活性对NO生成具有抑制作用,因此可作为一种抗炎剂。

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