Department of Bioscience and Biotechnology, Konkuk University, Seoul, Republic of Korea.
J Med Food. 2010 Dec;13(6):1468-77. doi: 10.1089/jmf.2010.1131. Epub 2010 Sep 27.
The immunomodulatory activity of an organic extract of Phellinus linteus grown on slightly germinated brown rice (PBR) was previously demonstrated. Here, we investigated the possible anti-inflammatory activity of the PBR extract by analyzing its effect on the expression of macrophage-derived cytokines, chemokines, and mediator genes that participate in immune and inflammatory responses and diseases. The extract profoundly inhibited the induction of cytokines and chemokines, including tumor necrosis factor-α, chemokine (C-X-C motif) ligand-10, granulocyte-macrophage colony-stimulating factor, and interleukin-6, in lipopolysaccharide (LPS)-stimulated RAW264.7 mouse macrophage cells. It also greatly inhibited LPS-stimulated production of nitric oxide (NO) and prostaglandin E(2) in RAW264.7 cells by suppressing the expression of inducible NO synthase and cyclooxygenase-2. PBR extract inhibited NO production with a twofold lower half-maximal inhibitory concentration value than P. linteus extract. To elucidate the underlying mechanism of action, we examined the effect of the PBR extract on the LPS-induced phosphorylation of mitogen-activated protein kinases (MAPKs) in RAW264.7 cells. PBR extract greatly inhibited extracellular signal-regulated kinase and c-Jun N-terminal kinase phosphorylation and slightly inhibited p38 MAPK phosphorylation. It also significantly increased intracellular glutathione peroxidase activity and heme oxygenase-1 protein expression. Thus, the PBR extract has anti-inflammatory activity in LPS-stimulated RAW264.7 cells by virtue of its ability to suppress the production of inflammatory cytokines and chemokines via inhibition of MAPK activation and up-regulation of antioxidant activities.
先前已经证实,糙皮侧耳菌在略微发芽糙米(PBR)上生长的有机提取物具有免疫调节活性。在这里,我们通过分析其对参与免疫和炎症反应和疾病的巨噬细胞衍生细胞因子、趋化因子和介质基因表达的影响,研究了 PBR 提取物的可能抗炎活性。该提取物能强烈抑制细胞因子和趋化因子(包括肿瘤坏死因子-α、趋化因子(C-X-C 基序)配体 10、粒细胞-巨噬细胞集落刺激因子和白细胞介素-6)在脂多糖(LPS)刺激的 RAW264.7 小鼠巨噬细胞中的诱导。它还通过抑制诱导型一氧化氮合酶和环氧化酶-2 的表达,极大地抑制了 LPS 刺激的 RAW264.7 细胞中一氧化氮(NO)和前列腺素 E(2)的产生。PBR 提取物抑制 NO 产生的半最大抑制浓度值比 P. linteus 提取物低两倍。为了阐明其作用机制,我们研究了 PBR 提取物对 LPS 诱导的 RAW264.7 细胞中丝裂原活化蛋白激酶(MAPKs)磷酸化的影响。PBR 提取物能强烈抑制细胞外信号调节激酶和 c-Jun N 末端激酶磷酸化,轻度抑制 p38 MAPK 磷酸化。它还显著增加了细胞内谷胱甘肽过氧化物酶活性和血红素加氧酶-1 蛋白的表达。因此,PBR 提取物通过抑制 MAPK 激活和上调抗氧化活性,抑制促炎细胞因子和趋化因子的产生,从而在 LPS 刺激的 RAW264.7 细胞中具有抗炎活性。