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裙带菜乙醇提取物对脂多糖刺激的 RAW 264.7 小鼠巨噬细胞的抗炎活性。

Anti-inflammatory activities of an ethanol extract of Ecklonia stolonifera in lipopolysaccharide-stimulated RAW 264.7 murine macrophage cells.

机构信息

Department of Food Science and Nutrition, Pukyong National University, Busan 608-737, South Korea.

出版信息

J Agric Food Chem. 2012 Sep 12;60(36):9120-9. doi: 10.1021/jf3022018. Epub 2012 Aug 28.

DOI:10.1021/jf3022018
PMID:22897701
Abstract

Ecklonia stolonifera is a brown alga that was shown to have antioxidant, anti-inflammatory, tyrosinase inhibitory, and chemopreventive activities. However, the molecular mechanisms underlying its anti-inflammatory activity remain unclear. In this study, we investigated the molecular mechanism of the anti-inflammatory action of E. stolonifera ethanolic extracts (ESE) using lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. ESE inhibited LPS-induced nitric oxide (IC(50) = 72 ± 1.9 μg/mL) and prostaglandin E(2) (IC(50) = 98 ± 5.3 μg/mL) production in a dose-dependent manner and suppressed the expression of inducible nitric oxide synthase and cyclooxygenase-2 in RAW 264.7 cells. ESE also reduced the production of pro-inflammatory cytokines in LPS-stimulated RAW 264.7 cells. LPS-induced nuclear factor-κB (NF-κB) transcriptional activity and NF-κB translocation into the nucleus were significantly inhibited by ESE treatment through the prevention of the degradation of inhibitor κB-α. Moreover, ESE inhibited the activation of Akt, ERK, JNK1/2, and p38 MAPK in LPS-stimulated RAW 264.7 cells. The main components with anti-inflammatory activity in ESE were identified as phlorofucofuroeckol A and B based on the inhibition of NO production. Our results indicate that ESE can be considered as a potential source of therapeutic agents for inflammatory diseases.

摘要

裙带菜是一种褐藻,具有抗氧化、抗炎、抑制酪氨酸酶和化学预防作用。然而,其抗炎活性的分子机制尚不清楚。在这项研究中,我们使用脂多糖(LPS)刺激的 RAW 264.7 细胞研究了裙带菜乙醇提取物(ESE)抗炎作用的分子机制。ESE 以剂量依赖性方式抑制 LPS 诱导的一氧化氮(IC50 = 72 ± 1.9 μg/mL)和前列腺素 E2(IC50 = 98 ± 5.3 μg/mL)的产生,并抑制 RAW 264.7 细胞中诱导型一氧化氮合酶和环氧化酶-2 的表达。ESE 还降低了 LPS 刺激的 RAW 264.7 细胞中促炎细胞因子的产生。ESE 通过阻止抑制剂 κB-α 的降解,显著抑制 LPS 诱导的核因子-κB(NF-κB)转录活性和 NF-κB 向核内易位。此外,ESE 抑制了 LPS 刺激的 RAW 264.7 细胞中 Akt、ERK、JNK1/2 和 p38 MAPK 的激活。根据 NO 产生的抑制作用,确定 ESE 中具有抗炎活性的主要成分是 phlorofucofuroeckol A 和 B。我们的结果表明,ESE 可以被认为是治疗炎症性疾病的潜在药物来源。

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