Anti-inflammatory potential of peat moss extracts in lipopolysaccharide-stimulated RAW 264.7 macrophages

被引:19
作者
Choi, Woo-Suk [1 ]
Jeong, Jin-Woo [2 ,3 ]
Kim, Sung Ok [4 ]
Kim, Gi-Young [5 ]
Kim, Byung-Woo [3 ,6 ]
Kim, Cheol Min [7 ]
Seo, Yong-Bae [1 ]
Kim, Woe-Yeon [8 ]
Lee, Sang-Yeol [8 ]
Jo, Kwon-Ho [9 ]
Choi, Young Ju [10 ]
Choi, Yung Hyun [2 ,3 ]
Kim, Gun-Do [1 ]
机构
[1] Pukyong Natl Univ, Coll Nat Sci, Dept Microbiol, Pusan 608737, South Korea
[2] Dong Eui Univ, Coll Oriental Med, Dept Biochem, Pusan 614052, South Korea
[3] Dong Eui Univ, Anti Aging Res Ctr & BlueBio Ind RIC, Pusan 614714, South Korea
[4] Daegu Haany Univ, Coll Oriental Med, Dept Herbal Pharmacol, Taegu 706828, South Korea
[5] Jeju Natl Univ, Dept Marine Life Sci, Immunobiol Lab, Cheju 690756, South Korea
[6] Dong Eui Univ, Dept Life Sci & Biotechnol, Pusan 614714, South Korea
[7] Busan Natl Univ, Coll Med, Dept Biochem, Yangsan 626870, South Korea
[8] Gyeongsang Natl Univ, Plant Mol Biol & Biotechnol Res Ctr, Div Appl Life Sci, Jinju 660701, South Korea
[9] Green Vortex Co Ltd, Pusan 614714, South Korea
[10] Silla Univ, Coll Med Life Sci, Dept Food & Nutr, Pusan 617736, South Korea
关键词
peat moss; anti-inflammation; nuclear factor-kappa B; mitogen-activated protein kinase; nuclear factor-like 2/heme oxygenase-1; NF-KAPPA-B; HEME OXYGENASE-1; NITRIC-OXIDE; TRANSCRIPTION FACTOR; POTASSIUM HUMATE; INFLAMMATORY RESPONSES; ENDOTHELIAL-CELLS; SIGNALING PATHWAY; OXIDATIVE STRESS; MAP KINASES;
D O I
10.3892/ijmm.2014.1881
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The aim of the present study was to identify the anti-inflammatory and anti-oxidative effects of peat moss aqueous extract (PME) on lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages. To demonstrate the anti-inflammatory and antioxidant effects of PME, the levels of nitric oxide (NO) and cytokines were measured using Griess reagent and cytokine ELISA kits, respectively. Reverse transcriptase-polymerase chain reaction (RT-PCR) and western blot analysis were conducted to evaluate the expression of genes and proteins. Immunofluorescence was used to measure the expression and translocation of transcription factors. Pre-treatment with PME inhibited the production of prostaglandin E-2 and NO by suppressing the gene expression of cyclooxygenase-2 and inducible NO synthase, respectively. The LPS-stimulated gene expression and the production of tumor necrosis factor-alpha and interleukin-1 beta were significantly reduced by PME. In the LPS-stimulated RAW 264.7 cells, nuclear factor-kappa B (NF-kappa B) translocated from the cytosol to the nucleus, while pre-treatment with PME induced the sequestration of NF-kappa B in the cytosol through the inhibition of I kappa B alpha degradation. In the same manner, PME contributed to the inhibition of the activation of mitogen-activated protein kinases. In addition, the PME-treated RAW 264.7 cells facilitated the activation of nuclear factor-like 2 (Nrf2), and in turn, enhanced heme oxygenase-1 (HO-1) expression. These results indicate that PME exerts anti-inflammatory and antioxidant effects, and suggest that PME may neutralize inflammation and prevent cellular damage by oxidative stress.
引用
收藏
页码:1101 / 1109
页数:9
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