Journal of Food and Nutrition Research
ISSN (Print): 2333-1119 ISSN (Online): 2333-1240 Website: http://www.sciepub.com/journal/jfnr Editor-in-chief: Prabhat Kumar Mandal
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Journal of Food and Nutrition Research. 2018, 6(1), 26-31
DOI: 10.12691/jfnr-6-1-5
Open AccessArticle

Anti-inflammatory Effects of Moutan Cortex Radicis Extract, Paeoniflorin and Oxypaeoniflorin through TLR Signaling Pathway in RAW264.7 Cells

Chang-Kil Yoo1, Ji-Hyun Hwang2, 3, Kippeum Lee2, Young-Jin Lee1, Kui-Jin Kim2, and Boo-Yong Lee2,

1Graduate School of Integrative Medicine, CHA University, Pocheon 11160, Republic of Korea

2Department of Food Science and Biotechnology, CHA University, Seongnam, Kyeonggi 463-400, Republic of Korea

3Systems Biotechnology Research Center, Korea Institute of Science and Technology (KIST), Gangneung 2541, Republic of Korea

Pub. Date: January 05, 2018

Cite this paper:
Chang-Kil Yoo, Ji-Hyun Hwang, Kippeum Lee, Young-Jin Lee, Kui-Jin Kim and Boo-Yong Lee. Anti-inflammatory Effects of Moutan Cortex Radicis Extract, Paeoniflorin and Oxypaeoniflorin through TLR Signaling Pathway in RAW264.7 Cells. Journal of Food and Nutrition Research. 2018; 6(1):26-31. doi: 10.12691/jfnr-6-1-5

Abstract

Moutan cortex radicis (MCR), the root bark of Paeonia suffruticosa, has been widely used as a traditional herb. In this study, we evaluated whether the MCR extract and two active compounds of the bark, paeoniflorin (paeo) and oxypaeoniflorin (oxypaeo), alleviate lipopolysaccharide (LPS)-induced inflammatory responses in RAW264.7 cells and whether they controlled TLR signaling pathway. RAW264.7 cells were treated with the MCR extract or two active compounds in the presence or absence of LPS. The extract and two active compounds inhibited LPS-stimulated nitric oxide (NO) production and inducible nitric oxide synthase (iNOS) gene expression. Additionally, the extract and two active compounds suppressed inflammatory cytokine secretion and gene expression in LPS-stimulated cells. The extract and two active compounds alleviated NF-κB activation by regulating upstream genes in TLR signaling pathway. In addition, the extract and two active compounds decreased phosphorylation of ERK and p38 MAPK. These results indicate that the MCR extract, paeo and oxypaeo have anti-inflammatory effects through regulation of TLR signaling pathway in RAW264.7 cells.

Keywords:
Moutan cortex radicis extract paeoniflorin oxypaeoniflorin inflammation TLR4 NF-κB IRF3 MAPKs

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

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References:

[1]  Hwang, J.H., K.J. Kim, S.J. Ryu, and B.Y. Lee, Caffeine prevents LPS-induced inflammatory responses in RAW264.7 cells and zebrafish. Chemico-biological interactions, 2016. 248: p. 1-7.
 
[2]  Cho, H.J., M.R. Seon, Y.M. Lee, J. Kim, J.K. Kim, S.G. Kim, and J.H. Park, 3,3'-Diindolylmethane suppresses the inflammatory response to lipopolysaccharide in murine macrophages. The Journal of nutrition, 2008. 138(1): p. 17-23.
 
[3]  Hofseth, L.J. and L. Ying, Identifying and defusing weapons of mass inflammation in carcinogenesis. Biochimica et biophysica acta, 2006. 1765(1): p. 74-84.
 
[4]  Takeuchi, O. and S. Akira, Pattern recognition receptors and inflammation. Cell, 2010. 140(6): p. 805-20.
 
[5]  Kawai, T. and S. Akira, TLR signaling. Cell death and differentiation, 2006. 13(5): p. 816-25.
 
[6]  Lu, Y.C., W.C. Yeh, and P.S. Ohashi, LPS/TLR4 signal transduction pathway. Cytokine, 2008. 42(2): p. 145-51.
 
[7]  Takeda, K. and S. Akira, TLR signaling pathways. Seminars in immunology, 2004. 16(1): p. 3-9.
 
[8]  Wieland, C.W., S. Florquin, N.A. Maris, K. Hoebe, B. Beutler, K. Takeda, S. Akira, and T. van der Poll, The MyD88-dependent, but not the MyD88-independent, pathway of TLR4 signaling is important in clearing nontypeable haemophilus influenzae from the mouse lung. The Journal of Immunology, 2005. 175(9): p. 6042-6049.
 
[9]  Huang, P., J. Han, and L. Hui, MAPK signaling in inflammation-associated cancer development. Protein & cell, 2010. 1(3): p. 218-26.
 
[10]  Wagner, E.F. and A.R. Nebreda, Signal integration by JNK and p38 MAPK pathways in cancer development. Nature reviews. Cancer, 2009. 9(8): p. 537-49.
 
[11]  Karin, M., Y. Yamamoto, and Q.M. Wang, The IKK NF-kappa B system: a treasure trove for drug development. Nature reviews. Drug discovery, 2004. 3(1): p. 17-26.
 
[12]  Choi, J., K.J. Kim, B.H. Kim, E.J. Koh, M.J. Seo, and B.Y. Lee, 6-Gingerol Suppresses Adipocyte-Derived Mediators of Inflammation In Vitro and in High-Fat Diet-Induced Obese Zebra Fish. Planta medica, 2017. 83(3-04): p. 245-253.
 
[13]  Yun, C.S., Y.G. Choi, M.Y. Jeong, J.H. Lee, and S. Lim, Moutan Cortex Radicis inhibits inflammatory changes of gene expression in lipopolysaccharide-stimulated gingival fibroblasts. Journal of natural medicines, 2013. 67(3): p. 576-89.
 
[14]  Jang, M.H., K.Y. Kim, P.H. Song, S.Y. Baek, H.L. Seo, E.H. Lee, S.G. Lee, K.I. Park, S.C. Ahn, S.C. Kim, and Y.W. Kim, Moutan Cortex Protects Hepatocytes against Oxidative Injury through AMP-Activated Protein Kinase Pathway. Biological & pharmaceutical bulletin, 2017. 40(6): p. 797-806.
 
[15]  Mao, Q.Q., X.M. Zhong, C.R. Feng, A.J. Pan, Z.Y. Li, and Z. Huang, Protective effects of paeoniflorin against glutamate-induced neurotoxicity in PC12 cells via antioxidant mechanisms and Ca(2+) antagonism. Cellular and molecular neurobiology, 2010. 30(7): p. 1059-66.
 
[16]  Liu, D.Z., K.Q. Xie, X.Q. Ji, Y. Ye, C.L. Jiang, and X.Z. Zhu, Neuroprotective effect of paeoniflorin on cerebral ischemic rat by activating adenosine A1 receptor in a manner different from its classical agonists. British journal of pharmacology, 2005. 146(4): p. 604-11.
 
[17]  Katsuyama, K., M. Shichiri, F. Marumo, and Y. Hirata, NO inhibits cytokine-induced iNOS expression and NF-kappaB activation by interfering with phosphorylation and degradation of IkappaB-alpha. Arteriosclerosis, thrombosis, and vascular biology, 1998. 18(11): p. 1796-802.
 
[18]  Takeda, K. and S. Akira, Toll-like receptors in innate immunity. International immunology, 2005. 17(1): p. 1-14.
 
[19]  Barton, G.M. and R. Medzhitov, Toll-like receptor signaling pathways. Science, 2003. 300(5625): p. 1524-5.
 
[20]  Hwang, J.H., K.J. Kim, and B.Y. Lee, Crude Ecklonia cava Flake Extracts Attenuate Inflammation through the Regulation of TLR4 Signaling Pathway in LPS-Induced RAW264.7 Cells. Molecules, 2017. 22(5).
 
[21]  Cheng, P., T. Wang, W. Li, I. Muhammad, H. Wang, X. Sun, Y. Yang, J. Li, T. Xiao, and X. Zhang, Baicalin Alleviates Lipopolysaccharide-Induced Liver Inflammation in Chicken by Suppressing TLR4-Mediated NF-kappaB Pathway. Frontiers in pharmacology, 2017. 8: p. 547.
 
[22]  Tak, P.P. and G.S. Firestein, NF-kappaB: a key role in inflammatory diseases. The Journal of clinical investigation, 2001. 107(1): p. 7-11.
 
[23]  Vanden Berghe, W., S. Plaisance, E. Boone, K. De Bosscher, M.L. Schmitz, W. Fiers, and G. Haegeman, p38 and extracellular signal-regulated kinase mitogen-activated protein kinase pathways are required for nuclear factor-kappaB p65 transactivation mediated by tumor necrosis factor. The Journal of biological chemistry, 1998. 273(6): p. 3285-90.