Aged red garlic extract reduces lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophages and acute pulmonary inflammation through haeme oxygenase-1 induction

被引:54
作者
Park, H. -J. [1 ]
Jeon, B. T. [2 ]
Kim, H. C. [3 ]
Roh, G. S. [2 ]
Shin, J. -H. [4 ]
Sung, N. -J. [4 ,5 ]
Han, J. [1 ]
Kang, D. [1 ]
机构
[1] Gyeongsang Natl Univ, Dept Physiol, Sch Med, Jinju 660751, South Korea
[2] Gyeongsang Natl Univ, Dept Anat, Sch Med, Jinju 660751, South Korea
[3] Gyeongsang Natl Univ, Dept Internal Med, Inst Hlth Sci, Sch Med, Jinju 660751, South Korea
[4] Namhae Garl Res Inst, Namhae, South Korea
[5] Gyeongsang Natl Univ, Dept Food & Nutr, Inst Agr & Life Sci, Jinju 660751, South Korea
基金
新加坡国家研究基金会;
关键词
garlic; haeme oxygenase-1; lipopolysaccharide; macrophage; nitric oxide; ANTIOXIDANT; INHIBITION; CELLS; MODEL; HEALTH;
D O I
10.1111/j.1748-1716.2012.02425.x
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
Aim It is known that garlic has antioxidative and anti-inflammatory properties. Aged red garlic (ARG), a novel aged garlic formulation, has higher antioxidant effects than fresh raw garlic. This study was performed to examine the anti-inflammatory effects of ARG extract (ARGE). Methods The anti-inflammatory effects of ARGE were evaluated in the lipopolysaccharide (LPS)-treated Raw 264.7 macrophages and acute lung inflammatory mice. NO production was determined by the Griess method, and iNOS, HO-1 and COX-2 expressions were measured using Western blot analysis. Histology and inflammation extent of lung were analysed using haematoxylin-eosin staining and immunohistochemistry. Results ARGE treatment markedly reduced LPS-induced nitrite production in RAW 264.7 macrophages and reduced inducible nitric oxide synthase (iNOS) expression. Treatment of cells with ARGE led to a significant increase in haeme oxygenase-1 (HO-1) protein expression, which was mediated by stimulating the expression of nuclear factor erythroid 2-related factor 2 (Nrf2). Treatment with zinc protoporphyrin, a selective inhibitor of HO-1, significantly reversed the ARGE-mediated inhibition of nitrite production (P < 0.05). In LPS-induced inflammatory mice, ARGE treatment down-regulated iNOS and COX-2 expressions, while it up-regulated HO-1 expression. Conclusion These results show that ARGE reduces LPS-induced nitric oxide production in RAW 264.7 macrophages through HO-1 induction and suggest that ARGE may have potential effects on prevention and treatment of acute inflammatory lung injury.
引用
收藏
页码:61 / 70
页数:10
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