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平行的体外和计算机研究非prenylated 芪类化合物的抗炎作用。

Parallel in vitro and in silico investigations into anti-inflammatory effects of non-prenylated stilbenoids.

机构信息

Department of Natural Drugs, University of Veterinary and Pharmaceutical Sciences Brno, Palackého třída 1946/1, 61242 Brno, Czech Republic; Department of Molecular Biology and Pharmaceutical Biotechnology, University of Veterinary and Pharmaceutical Sciences Brno, Palackého třída 1946/1, 61242 Brno, Czech Republic.

Department of Natural Drugs, University of Veterinary and Pharmaceutical Sciences Brno, Palackého třída 1946/1, 61242 Brno, Czech Republic.

出版信息

Food Chem. 2019 Jul 1;285:431-440. doi: 10.1016/j.foodchem.2019.01.128. Epub 2019 Jan 31.

Abstract

Stilbenoids represent a large group of bioactive compounds, which occur in food and medicinal plants. Twenty-five stilbenoids were screened in vitro for their ability to inhibit COX-1, COX-2 and 5-LOX. Piceatannol and pinostilbene showed activity comparable to the zileuton and ibuprofen, respectively. The anti-inflammatory potential of stilbenoids was further evaluated using THP-1 human monocytic leukemia cell line. Tests of the cytotoxicity on the THP-1 and HCT116 cell lines showed very low toxic effects. The tested stilbenoids were evaluated for their ability to attenuate the LPS-stimulated activation of NF-κB/AP-1. Most of the tested substances reduced the activity of NF-κB/AP-1 and later attenuated the expression of TNF-α. The effects of selected stilbenoids were further investigated on inflammatory signaling pathways. Non-prenylated stilbenoids regulated attenuation of NF-ĸB/AP-1 activity upstream by inhibiting the phosphorylation of MAPKs. A docking study used to in silico analyze the tested compounds confirmed their interaction with NF-ĸB, COX-2 and 5-LOX.

摘要

芪类化合物是一大类生物活性化合物,存在于食物和药用植物中。本研究筛选了 25 种芪类化合物,以评估它们抑制 COX-1、COX-2 和 5-LOX 的能力。白藜芦醇和紫檀芪的活性分别与齐留通和布洛芬相当。通过 THP-1 人单核白血病细胞系进一步评估了芪类化合物的抗炎潜力。在 THP-1 和 HCT116 细胞系上的细胞毒性测试显示出非常低的毒性作用。对测试的芪类化合物进行了评估,以确定它们减轻 LPS 刺激的 NF-κB/AP-1 激活的能力。大多数测试物质降低了 NF-κB/AP-1 的活性,随后减弱了 TNF-α 的表达。进一步研究了选定芪类化合物对炎症信号通路的影响。非 prenylated 芪类化合物通过抑制 MAPKs 的磷酸化,在上游调节 NF-ĸB/AP-1 活性的衰减。使用对接研究在计算机上分析了测试化合物,证实了它们与 NF-ĸB、COX-2 和 5-LOX 的相互作用。

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