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乙酸沉香酯是一种从乳香树脂中分离出的新型抗炎化合物,可抑制核因子-κB的激活。

Incensole acetate, a novel anti-inflammatory compound isolated from Boswellia resin, inhibits nuclear factor-kappa B activation.

作者信息

Moussaieff Arieh, Shohami Esther, Kashman Yoel, Fride Ester, Schmitz M Lienhard, Renner Florian, Fiebich Bernd L, Munoz Eduardo, Ben-Neriah Yinon, Mechoulam Raphael

机构信息

Department of Medicinal Chemistry and Natural Products, Medical Faculty, Hebrew University, Jerusalem 91120, Israel.

出版信息

Mol Pharmacol. 2007 Dec;72(6):1657-64. doi: 10.1124/mol.107.038810. Epub 2007 Sep 25.

Abstract

Boswellia resin is a major anti-inflammatory agent in herbal medical tradition, as well as a common food supplement. Its anti-inflammatory activity has been attributed to boswellic acid and its derivatives. Here, we re-examined the anti-inflammatory effect of the resin, using inhibitor of nuclear factor-kappaB alpha (IkappaB alpha) degradation in tumor necrosis factor (TNF) alpha-stimulated HeLa cells for a bioassay-guided fractionation. We thus isolated two novel nuclear factor-kappaB (NF-kappaB) inhibitors from the resin, their structures elucidated as incensole acetate (IA) and its nonacetylated form, incensole (IN). IA inhibited TAK/TAB-mediated IkappaB kinase (IKK) activation loop phosphorylation, resulting in the inhibition of cytokine and lipopolysaccharide-mediated NF-kappaB activation. It had no effect on IKK activity in vitro, and it did not suppress IkappaB alpha phosphorylation in costimulated T-cells, indicating that the kinase inhibition is neither direct nor does it affect all NF-kappaB activation pathways. The inhibitory effect seems specific; IA did not interfere with TNFalpha-induced activation of c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinase. IA treatment had a robust anti-inflammatory effect in a mouse inflamed paw model. Cembrenoid diterpenoids, specifically IA and its derivatives, may thus constitute a potential novel group of NF-kappaB inhibitors, originating from an ancient anti-inflammatory herbal remedy.

摘要

乳香树脂是草药医学传统中的一种主要抗炎剂,也是一种常见的食品补充剂。其抗炎活性归因于乳香酸及其衍生物。在此,我们重新研究了该树脂的抗炎作用,利用肿瘤坏死因子(TNF)α刺激的HeLa细胞中核因子-κBα(IkappaBα)降解抑制剂进行生物测定导向的分级分离。我们由此从该树脂中分离出两种新型核因子-κB(NF-κB)抑制剂,其结构被阐明为醋酸焚香醇(IA)及其非乙酰化形式焚香醇(IN)。IA抑制TAK/TAB介导的IkappaB激酶(IKK)激活环磷酸化,从而抑制细胞因子和脂多糖介导的NF-κB激活。它在体外对IKK活性没有影响,并且在共刺激的T细胞中不抑制IkappaBα磷酸化,表明激酶抑制既不是直接的,也不影响所有的NF-κB激活途径。这种抑制作用似乎具有特异性;IA不干扰TNFα诱导的c-Jun氨基末端激酶(JNK)和p38丝裂原活化蛋白激酶的激活。在小鼠炎症爪模型中,IA治疗具有强大的抗炎作用。因此,松香烷二萜类化合物,特别是IA及其衍生物,可能构成一组潜在的新型NF-κB抑制剂,源自一种古老的抗炎草药。

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