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黄芩短梗变种 Stapf 和通过调控 NF-κB/COX-2/iNOS 通路发挥抗炎作用的活性成分。

Scutellaria brevibracteata Stapf and active principles with anti-inflammatory effects through regulation of NF-κB/COX-2/iNOS pathways.

机构信息

Department of Pharmacognosy, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey.

Department of Pharmacology, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey.

出版信息

Fitoterapia. 2022 Apr;158:105159. doi: 10.1016/j.fitote.2022.105159. Epub 2022 Feb 14.

Abstract

Inflammation is a critical defense mechanism for body which is crucial for wound healing. However, when it spirals out of control and becomes chronic, it possesses a risk for diseases such as metabolic disorders or cancer. Scutellaria L. species are known with their potent anti-inflammatory effects. We aim to investigate the potential anti-inflammatory effects of Scutellaria brevibracteata Stapf and its active principles with underlying mechanisms using both in vitro and in vivo methods. Aqueous extract of S. brevibracteata (SB) was chromatographed on several columns to get 6 main fractions and 2 pure compounds. The levels of IL-6, NO, and TNF-α were measured in LPS-induced RAW 264.7 cells. In vivo carrageenan-induced paw edema test and immunoblotting in these paws were performed. SB was significantly reduced the inflammation in LPS-induced RAW cells via IL-6 and TNF-α cytokines at 200 μg/mL (P < 0.001) and paw edema via COX-2 and iNOS (P < 0.001). 3-O-methyl kaempferol, isolated from SB, reduced the production of NO, IL-6 and TNF-α in LPS-stimulated macrophages at 50 μM (P < 0.001); it significantly diminished inflammation-induced edema and COX-2, iNOS, and NF-κB protein levels were reduced compared to control group (P < 0.001). It was noticed that the methoxylation of C3 position has no effect on the anti-inflammatory mechanism of action comparing with kaempferol. In vivo studies indicated 3-O-methyl kaempferol was as effective as indomethacin. Considering the side effects caused by indomethacin, this compound can be evaluated as a novel drug candidate in inflammatory diseases with fewer side effects.

摘要

炎症是身体的一种关键防御机制,对于伤口愈合至关重要。然而,当它失去控制并变得慢性时,就会对代谢紊乱或癌症等疾病构成风险。黄芩属植物以其强大的抗炎作用而闻名。我们旨在使用体外和体内方法研究短序黄芩的潜在抗炎作用及其活性成分及其潜在机制。短序黄芩的水提物(SB)经几种柱层析得到 6 个主要馏分和 2 个纯化合物。测量 LPS 诱导的 RAW 264.7 细胞中 IL-6、NO 和 TNF-α 的水平。在这些爪子中进行了角叉菜胶诱导的爪肿胀试验和免疫印迹。SB 通过 200μg/mL(P<0.001)的 IL-6 和 TNF-α 细胞因子和 COX-2 和 iNOS(P<0.001)显著降低了 LPS 诱导的 RAW 细胞中的炎症。从 SB 中分离出的 3-O-甲基山奈酚在 50μM 时降低了 LPS 刺激的巨噬细胞中 NO、IL-6 和 TNF-α 的产生(P<0.001);与对照组相比,它显著减少了炎症诱导的水肿和 COX-2、iNOS 和 NF-κB 蛋白水平的降低(P<0.001)。注意到 C3 位的甲氧基化对山奈酚的抗炎作用机制没有影响。体内研究表明,3-O-甲基山奈酚与吲哚美辛一样有效。考虑到吲哚美辛引起的副作用,该化合物可以作为一种新型药物候选物,用于治疗炎症性疾病,副作用更少。

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