Moutan Cortex Radicis inhibits inflammatory changes of gene expression in lipopolysaccharide-stimulated gingival fibroblasts

被引:47
作者
Yun, Cheol-Sang [1 ]
Choi, Yeong-Gon [1 ,2 ]
Jeong, Mi-Young [1 ,2 ]
Lee, Je-Hyun [3 ]
Lim, Sabina [1 ,2 ]
机构
[1] Kyung Hee Univ, Coll Oriental Med, Dept Basic Oriental Med Sci, Seoul 130701, South Korea
[2] Kyung Hee Univ, East West Med Res Inst, WHO Collaborating Ctr Tradit Med, Res Grp Pain & Neurosci, Seoul 130701, South Korea
[3] Dongguk Univ, Dept Herbol, Coll Oriental Med, Gyeongju, South Korea
关键词
Anti-inflammation; Gene array; HPLC; Periodontal disease; NECROSIS-FACTOR-ALPHA; ACTIVATED T-CELLS; INTERFERON-GAMMA; INDUCIBLE PROTEIN-10; DENDRITIC CELLS; DECOY RECEPTOR; PAEONIA-SUFFRUTICOSA; IDO EXPRESSION; CXC-CHEMOKINE; INTERLEUKIN-8;
D O I
10.1007/s11418-012-0714-3
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Moutan Cortex Radicis (MCR), the root bark of Paeonia suffruticosa Andrews (Paeoniaceae), is found in the traditional Chinese medicinal formulae which were used to treat periodontal diseases. This study investigated the changes in gene expression by MCR treatment when stimulated with lipopolysaccharide (LPS) in cultured human gingival fibroblasts (HGFs). A genome-wide expression GeneChip was used for the gene array analysis, and real-time reverse transcription polymerase chain reaction (RT-PCR) analysis was also performed to confirm the gene expression. It was shown that 42 of the 643 genes up-regulated by LPS, when compared to the control, were down-regulated by the MCR treatment. Of these 42 genes, the inflammation and immune response-related genes were especially noted, which indicates that MCR inhibits the induction of inflammation by LPS stimulation. In addition, 33 of the 519 genes down-regulated by LPS, when compared to the control, were up-regulated by the MCR treatment. The expression patterns of some representative genes by real-time RT-PCR correlated with those of the genes shown in the microarray. In addition, the MCR extract contained paeonol and paeoniflorin, which are known to have the anti-inflammatory effect as the major phenolic components of MCR. This study showed that the MCR extract could comprehensively inhibit a wide variety of activations of inflammation-related genes, which may be due to paeonol and paeoniflorin. It is, thus, suggested that MCR may be applied to alleviate the inflammation of periodontal diseases.
引用
收藏
页码:576 / 589
页数:14
相关论文
共 57 条
[1]   Opposing effects of monomeric and pentameric C-reactive protein on endothelial progenitor cells [J].
Ahrens, I. ;
Domeij, H. ;
Eisenhardt, S. U. ;
Topcic, D. ;
Albrecht, M. ;
Leitner, E. ;
Viitaniemi, K. ;
Jowett, J. B. ;
Lappas, M. ;
Bode, C. ;
Haviv, I. ;
Peter, K. .
BASIC RESEARCH IN CARDIOLOGY, 2011, 106 (05) :879-895
[2]   Identification of Gliotropic Factors That Induce Human Stem Cell Migration to Malignant Tumor [J].
An, Jeung Hee ;
Lee, Soo Youn ;
Jeon, Jeong Yong ;
Cho, Kyung Gi ;
Kim, Seong U. ;
Lee, Myung Ae .
JOURNAL OF PROTEOME RESEARCH, 2009, 8 (06) :2873-2881
[3]   HUMAN INTERFERON-INDUCIBLE PROTEIN-10 IS A POTENT INHIBITOR OF ANGIOGENESIS IN-VIVO [J].
ANGIOLILLO, AL ;
SGADARI, C ;
TAUB, DD ;
LIAO, F ;
FARBER, JM ;
MAHESHWARI, S ;
KLEINMAN, HK ;
REAMAN, GH ;
TOSATO, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (01) :155-162
[4]   A comparison of HIV-1 integrase inhibition by aqueous and methanol extracts of Chinese medicinal herbs [J].
Au, TK ;
Lam, TL ;
Ng, TB ;
Fong, WP ;
Wan, DCC .
LIFE SCIENCES, 2001, 68 (14) :1687-1694
[5]   Chemokine IP-10 expression in cultured human keratinocytes [J].
Boorsma, DM ;
Flier, J ;
Sampat, S ;
Ottevanger, C ;
de Haan, P ;
Hooft, L ;
Willemze, R ;
Tensen, CP ;
Stoof, TJ .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1998, 290 (06) :335-341
[6]   The CXCR3 binding chemokine IP-10/CXCL10: Structure and receptor interactions [J].
Booth, V ;
Keizer, DW ;
Kamphuis, MB ;
Clark-Lewis, I ;
Sykes, BD .
BIOCHEMISTRY, 2002, 41 (33) :10418-10425
[7]   Interferon-inducible T cell alpha chemoattractant (I-TAC): A novel non-ELR CXC chemokine with potent activity on activated T cells through selective high affinity binding to CXCR3 [J].
Cole, KE ;
Strick, CA ;
Paradis, TJ ;
Ogborne, KT ;
Loetscher, M ;
Gladue, RP ;
Lin, W ;
Boyd, JG ;
Moser, B ;
Wood, DE ;
Sahagan, BG ;
Neote, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (12) :2009-2021
[8]   Human gingival fibroblasts produce nitric oxide in response to proinflammatory cytokines [J].
Daghigh, F ;
Borghaei, RC ;
Thornton, RD ;
Bee, JH .
JOURNAL OF PERIODONTOLOGY, 2002, 73 (04) :392-400
[9]  
Ding HY, 1999, CHEM PHARM BULL, V47, P652
[10]   IFN-γ-Inducible protein 10 (IP-10; CXCL10)-deficient mice reveal a role for IP-10 in effector T cell generation and trafficking [J].
Dufour, JH ;
Dziejman, M ;
Liu, MT ;
Leung, JH ;
Lane, TE ;
Luster, AD .
JOURNAL OF IMMUNOLOGY, 2002, 168 (07) :3195-3204