Anti-inflammatory effects of methanol extract of Patrinia scabiosaefolia in mice with ulcerative colitis

被引:116
作者
Cho, Eu-jin [1 ,2 ]
Shin, Ji-Sun [1 ,2 ]
Noh, Young-Su [1 ,2 ]
Cho, Young-Wuk [2 ]
Hong, Seung-Jae [2 ]
Park, Jae-Hoon [2 ]
Lee, Jae Yeol [3 ]
Lee, Jin-Yong [4 ]
Lee, Kyung-Tae [1 ,2 ]
机构
[1] Kyung Hee Univ, Dept Pharmaceut Biochem, Coll Pharm, Seoul 130701, South Korea
[2] Kyung Hee Univ, Dept Biomed Sci, Coll Med Sci, Seoul 130701, South Korea
[3] Kyung Hee Univ, Dept Chem, Coll Sci, Seoul 130701, South Korea
[4] Kyung Hee Univ, Coll Oriental Med, Seoul 130701, South Korea
关键词
Patrinia scabiosaefolia; Ulcerative colitis; DSS; INFLAMMATORY-BOWEL-DISEASE; DEXTRAN SULFATE SODIUM; NITRIC-OXIDE SYNTHASE; RECEPTOR ANTAGONIST; URSOLIC ACID; IN-VIVO; EXPRESSION; THERAPY; CELLS; MODEL;
D O I
10.1016/j.jep.2010.04.047
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Ethnopharmacological relevance: Patrinia scabiosaefolia Fisch is used in folk medicines to treat intestinal abscesses, acute appendicitis, and dysentery in Asia. Although recent reports indicate that Patrinia scabiosaefolia has sedative and anti-tumor effects, its effects on ulcerative colitis have not been previously explored. Aim of the study: To determine the effects and the mode of action of the methanol extract of the roots of Patrinia scabiosaefolia (PME) on a model of colitis in mice induced by dextran sulfate sodium (DSS). Materials and methods: We induced colitis using DSS in 5-week-ICR mice over 7 days and estimated disease activity index (DAI), which took into account body weight, stool consistency, gross bleeding, and tissue myeloperoxidase (MPO) accumulation. Colon lengths and spleen weights were measured. Histological changes were observed by H&E staining. Pro-inflammatory mediators, namely, nitric oxide (NO), tumor necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1 beta), and interleukin-6 (IL-6), were determined using Griess assays, immunoassays, and by quantitative real-time reverse-transcriptase polymerase chain reaction (qRT-PCR), respectively. Results: PME significantly attenuated DSS-induced DAI scores and tissue MPO accumulation, which implied that it suppressed weight loss, diarrhea, gross bleeding, and the infiltrations of immune cells. PME administration also effectively and dose-dependently prevented shortening of colon length and enlargement of spleen size. Histological examinations indicated that PME suppressed edema, mucosal damage, and the loss of crypts induced by DSS. Furthermore, PME inhibited the abnormal secretions and mRNA expressions of pro-inflammatory cytokines, such as, TNF-alpha, IL-1 beta, and IL-6. Conclusion: These results suggest that PME has an anti-inflammatory effect at colorectal sites that is due to the down-regulations of the productions and expressions of inflammatory mediators, and that it may have therapeutic value in the setting of inflammatory bowel disease (IBD). (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:428 / 435
页数:8
相关论文
共 53 条
[1]
[Anonymous], COCHRANE DATABASE SY
[2]
Biologic therapy for inflammatory bowel disease [J].
Ardizzone, S ;
Porro, GB .
DRUGS, 2005, 65 (16) :2253-2286
[3]
Asakura H, 1998, Nihon Rinsho, V56, P2354
[4]
Mast cells are an important cellular source of tumour necrosis factor α in human intestinal tissue [J].
Bischoff, SC ;
Lorentz, A ;
Schwengberg, S ;
Weier, G ;
Raab, R ;
Manns, MP .
GUT, 1999, 44 (05) :643-652
[5]
BOUGHTONSMITH NK, 1994, J ROY SOC MED, V87, P312
[6]
5-aminosalicylic acid and olsalazine inhibit tumor growth in a rodent model of colorectal cancer [J].
Brown, WA ;
Farmer, KC ;
Skinner, SA ;
Malcontenti-Wilson, C ;
Misajon, A ;
O'Brien, PE .
DIGESTIVE DISEASES AND SCIENCES, 2000, 45 (08) :1578-1584
[7]
CHANG HM, 1987, PHARM APPL CHINESE M, V2, P745
[8]
Ethyl acetate extract of Patrinia scabiosaefolia downregulates anti-apoptotic Bcl-2/BCI-XL expression, and induces apoptosis in human breast carcinoma MCF-7 cells independent of caspase-9 activation [J].
Chiu, LCM ;
Ho, TS ;
Wong, EYL ;
Ooi, VEC .
JOURNAL OF ETHNOPHARMACOLOGY, 2006, 105 (1-2) :263-268
[9]
Implication of TNF-α convertase (TACE/ADAM17) in inducible nitric oxide synthase expression and inflammation in an experimental model of colitis [J].
Colón, AL ;
Menchén, LA ;
Hurtado, O ;
De Cristóbal, J ;
Lizasoain, I ;
Leza, JC ;
Lorenzo, P ;
Moro, MA .
CYTOKINE, 2001, 16 (06) :220-226
[10]
Nitric oxide in inflammatory bowel disease [J].
Cross, RK ;
Wilson, KT .
INFLAMMATORY BOWEL DISEASES, 2003, 9 (03) :179-189