Anti-inflammatory Activity of Saxifragin via Inhibition of NF-κB Involves Caspase-1 Activation

被引:26
作者
Cheon, Se-Yun [1 ]
Chung, Kyung-Sook [1 ]
Jeon, Eunjin [1 ]
Nugroho, Agung [2 ]
Park, Hee-Jun [3 ]
An, Hyo-Jin [1 ]
机构
[1] Sangji Univ, Coll Oriental Med, Dept Pharmacol, Gangwon Do 220702, South Korea
[2] Lambing Mangkurat Univ, Dept Agroind Technol, Banjarbaru, Indonesia
[3] Sangji Univ, Coll Hlth Sci, Dept Pharmaceut Engn, Wonju, South Korea
来源
JOURNAL OF NATURAL PRODUCTS | 2015年 / 78卷 / 07期
基金
新加坡国家研究基金会;
关键词
NITRIC-OXIDE SYNTHASE; INFLAMMASOME ACTIVATION; MURINE MACROPHAGES; RECRUITMENT DOMAIN; NUCLEAR-FACTOR; LIPOPOLYSACCHARIDE; CELLS; P38; CYCLOOXYGENASE-2; TRANSCRIPTION;
D O I
10.1021/acs.jnatprod.5b00145
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Saxifragin, the 5-glucoside of the flavonoid quercetin, is found in plants and insects. It has been reported that saxifragin has peroxynitrite-scavenging effects. However, the mechanism of anti-inflammatory effects of saxifragin has not yet been clearly identified. In this study, we investigated the anti-inflammatory effects of saxifragin in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages and animal models of inflammation. We found that saxifragin suppressed the production of nitric oxide (NO) and prostaglandin E-2 (PGE(2)) in LPS-activated RAW 264.7 macrophages by suppressing the level of protein and mRNA expression of inducible nitric oxide synthase (iNOS) and cydooxygenase-2 (COX-2), respectively. Furthermore, saxifragin inhibited mRNA expression of pro-inflammatory cytokines including tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, and IL-1 beta. We studied the inhibitory effects of saxifragin on the nuclear translocation of nuclear factor (NF)-kappa B, activation of caspase-1, and phosphorylation of c-Jun N-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK). Furthermore, pretreatment with saxifragin increased the survival rate of mice with LPS-induced septic death. Collectively, these findings suggest that saxifragin exerts anti-inflammatory activity by inhibiting NF-kappa B, caspase-1, and mitogen-activated protein kinase (MAPK) activation.
引用
收藏
页码:1579 / 1585
页数:7
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