Anti-inflammatory effects of methanol extracts of the root of Lilium lancifolium on LPS-stimulated Raw264.7 cells

被引:100
作者
Kwon, Ok-Kyoung [1 ]
Lee, Mee-Young [2 ]
Yuk, Ji-Eun [1 ]
Oh, Sei-Ryang [1 ]
Chin, Young-Won [1 ]
Lee, Hyeong-Kyu [1 ]
Ahn, Kyung-Seop [1 ]
机构
[1] Korea Res Inst Biosci & Biotechnol, Immune Modulator Res Ctr, Cheongwon Gun, Chungbuk, South Korea
[2] Korea Inst Oriental Med, EBM Res Ctr, Taejon 305811, South Korea
关键词
Lilium lancifolium; Inflammation; iNOS; COX-2; TNF-alpha; NF-kappa B; IL-4; IL-13; NITRIC-OXIDE SYNTHASE; KINASE; ACTIVATION; MACROPHAGES; NOS;
D O I
10.1016/j.jep.2010.04.002
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Aim of the study: Lilium lancifolium is commonly used to treat bronchitis, pneumonia, etc. In this study, we investigated the anti-inflammatory effects of methanol extracts of the root of Lilium lancifolium (LL extracts) in LPS-stimulated Raw264.7 cells. Material and methods: Levels of NO, PGE(2) and pro-inflammatory cytokines (IL-6 and TNF-alpha) in the supernatant fraction were determined using sandwich ELISA. Expression of COX-2 and iNOS, phosphorylation of MAPK subgroups (ERK and JNK), and NF-kappa B activation in extracts were detected via Western blot and immunocytochemistry assays. Results: The LL extract significantly inhibited NO, PGE(2), IL-6 and INF-alpha production in LPS-stimulated cells, and suppressed iNOS and COX-2 expression. A mechanism-based study showed that phosphorylation of ERK1/2 and JNK and translocation of the NF-kappa B p65 subunit into nuclei were inhibited by the LL extract. Furthermore, interleukin-4 and interleukin-13 production in Con A-induced splenocytes was suppressed. Conclusion: These results indicate that anti-inflammatory effects of methanol extracts from Lilium lancifolium are due to downregulation of iNOS and COX-2 via suppression of NF-kappa B activation and nuclear translocation as well as blocking of ERK and JNK signaling in LPS-stimulated Raw264.7 cells. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:28 / 34
页数:7
相关论文
共 26 条
[1]   Inflammation and cancer: How hot is the link? [J].
Aggarwal, Bharat B. ;
Shishodia, Shishir ;
Sandur, Santosh K. ;
Pandey, Manoj K. ;
Sethi, Gautam .
BIOCHEMICAL PHARMACOLOGY, 2006, 72 (11) :1605-1621
[2]   Nitric oxide and cell viability in inflammatory cells:: a role for NO in macrophage function and fate [J].
Boscá, L ;
Zeini, M ;
Travès, PG ;
Hortelano, S .
TOXICOLOGY, 2005, 208 (02) :249-258
[3]   Role of inducible nitric oxide synthase and NADPH oxidase in early control of Burkholderia pseudomallei infection in mice [J].
Breitbach, Katrin ;
Klocke, Sonja ;
Tschernig, Thomas ;
van Rooijen, Nico ;
Baumann, Ulrich ;
Steinmetz, Ivo .
INFECTION AND IMMUNITY, 2006, 74 (11) :6300-6309
[4]  
CHOI CR, 2003, DONGEEBOKAM JABBEONG
[5]   Sarcomas often express constitutive nitric oxide synthases (NOS) but infrequently inducible NOS [J].
Cunha, Isabela W. ;
Lopes, Ademar ;
Falzoni, Roberto ;
Soares, Fernando A. .
APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY, 2006, 14 (04) :404-410
[6]   Effects of macrophage inducible nitric oxide synthase in murine septic lung injury [J].
Farley, KS ;
Wang, LF ;
Razavi, HM ;
Law, C ;
Rohan, M ;
McCormack, DG ;
Mehta, S .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2006, 290 (06) :L1164-L1172
[7]   Oxygen metabolism by neuronal nitric-oxide synthase [J].
Gao, Ying Tong ;
Panda, Satya Prakash ;
Roman, Linda J. ;
Martasek, Pavel ;
Ishimura, Yuzuru ;
Masters, Bettie Sue S. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (11) :7921-7929
[8]  
GENG Y, 1993, J IMMUNOL, V151, P6692
[9]  
GEPPERT TD, 1994, MOL MED, V1, P93
[10]   Activation of c-Jun N-terminal kinase in bacterial lipopolysaccharide-stimulated macrophages [J].
Hambleton, J ;
Weinstein, SL ;
Lem, L ;
DeFranco, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (07) :2774-2778