RSS-Feed abonnieren
DOI: 10.1055/s-0029-1240701
© Georg Thieme Verlag KG Stuttgart · New York
Comparison of the Enteric Mucosal Immunomodulatory Activity of Combinations of Coptis chinensis Franch. Rhizomes and Evodia rutaecarpa (Juss.) Benth. Fruits in Mice with Dextran Sulphate Sodium-Induced Ulcerative Colitis
Publikationsverlauf
received May 10, 2009
revised Nov. 19, 2009
accepted Nov. 23, 2009
Publikationsdatum:
23. Dezember 2009 (online)

Abstract
Combinations of crude rhizomes of Coptis chinensis Franch., Ranunculaceae, and fruits of Evodia rutaecarpa (Juss.) Benth., Rutaceae, at a ratio of 6 : 1 (formula A) and 1 : 6 (formula B) were extracted with boiling water, and their modulatory activity on enteric mucosal immune responses in mice with dextran sulphate sodium-induced ulcerative colitis was investigated. The results showed that both formulas could reduce the severity of inflammation in the colon. Formula A at a low dose can decrease myeloperoxidase (MPO) activity, and formula B was inactive. Both formulas did not affect the percentages of CD4+ and CD8+ T cells in the periphery, but they evoked an increase of CD8+ T cells among the enteric intraepithelial lymphocytes. Formula B at a low dose could increase both CD4+ and CD8+ cells, and formula A at a high dose could only increase CD8+ T cells among the Peyer's patch lymphocytes (p < 0.05). Both formulas did not affect the percentages of CD4+ and CD8+ T cells among the lamina propria lymphocytes, but decreased the serum concentration of IL-1β (p < 0.05 at a low dose of formula A) and enhanced the level of IL-10 in serum (p < 0.05 at a low dose formula B). We conclude that both formulas have a similar modulating effect on enteric mucosal immune responses, the major difference being that formula A could decrease the level of IL-1 β, while formula B could increase the IL-10 dose in serum.
Key words
Ranunculaceae - Coptis chinensis Franch. - Rutaceae - Evodia rutaecarpa (Juss.) Benth. - ulcerative colitis - mice
References
- 1 Sun W J, Zhang Y J, Yao N, Jiang H, Wang Q. Influence on rat intestinal absorption of huanglian alkalis after match-pair of huanglian-wuzhuyu. Zhongguo Zhong Yao Za Zhi. 2008; 33 2614-2616
- 2 Xiao S, Du L, Wang Z, Bi K, Chen D, Yang Z. Research and development of wuzhuyu decoction. Zhongguo Zhong Yao Za Zhi. 1999; 24 503-504
- 3 Hirano H, Osawa E, Yamaoka Y, Yokoi T. Gastric-mucous membrane protection activity of coptisine derivatives. Biol Pharm Bull. 2001; 24 1277-1281
- 4 Hamasaki N, Ishii E, Tominaga K, Tezuka Y, Nagaoka T, Kadota S, Kuroki T, Yano I. Highly selective antibacterial activity of novel alkyl quinolone alkaloids from a Chinese herbal medicine, Gosyuyu (Wu-Chu-Yu), against Helicobacter pylori in vitro. Microbiol Immunol. 2000; 44 9-15
- 5 Karlinger K, Györke T, Makö E, Mester A, Tarján Z. The epidemiology and the pathogenesis of inflammatory bowel disease. Eur J Radiol. 2000; 35 154-167
- 6 MacDonald T T, Monteleone G. Immunity, inflammation, and allergy in the gut. Science. 2005; 307 1920-1925
- 7 Yu Y, Sitaraman S, Gewirtz A T. Intestinal epithelial cell regulation of mucosal inflammation. Immunol Res. 2004; 29 55-68
- 8 Hong Y, Hui S C, Chan T Y, Hou J Y. Effect of berberine on regression of pressure-overload induced cardiac hypertrophy in rats. Am J Chin Med. 2002; 30 589-599
- 9 Lee T J, Kim E J, Kim S, Jung E M, Park J W, Jeong S H, Park S E, Yoo Y H, Kwon T K. Caspase-dependent and caspase-independent apoptosis induced by evodiamine in human leukemic U937 cells. Mol Cancer Ther. 2006; 5 2398-2407
- 10 Okayasu I, Hatakeyama S, Yamada M, Ohkusa T, Inagaki Y, Nakaya R. A novel method in the induction of reliable experimental acute and chronic ulcerative colitis in mice. Gastroenterology. 1990; 98 694-702
- 11 Krawisz J E, Sharon P, Stenson W F. Quantitative assay for acute intestinal inflammation based on myeloperoxidase activity. Assessment of inflammation in rat and hamster models. Gastroenterology. 1984; 87 1344-1350
- 12 Todd D, Singh A J, Greiner D L, Mordes J P, Rossini A A, Bortell R. A new isolation method for rat intraepithelial lymphocyte. J Immunol Methods. 1999; 224 111-127
- 13 Xiao C, Lu C, Zhao L, Liu Z, Zhang W, He Y, Chen S, Tang J C, Chan A S, Lu A. The effects of triptolide on enteric mucosal immune responses of DBA/1 mice with collagen-induced arthritis. Planta Med. 2006; 72 1268-1272
- 14 Elson C O, Sartor R B, Tennyson G S, Riddell R H. Experimental models of inflammatory bowel disease. Gastroenterology. 1995; 109 1344-1367
- 15 Mayer L. Mucosal immunity and gastrointestinal antigen processing. J Pediatr Gastroenterol Nutr. 2000; 30 S4-S12
- 16 Nagler-Anderson C, Shi H N. Peripheral nonresponsiveness to orally administered soluble protein antigens. Crit Rev Immunol. 2001; 21 121-131
- 17 Powrie F. T cells in inflammatory bowel disease: protective and pathogenic roles. Immunity. 1995; 3 171-174
- 18 Podolsky D K. Lessons from genetic models of inflammatory bowel disease. Acta Gastroenterol Belg. 1997; 60 163-165
- 19 Coombes J L, Maloy K J. Control of intestinal homeostasis by regulatory T cells and dendritic cells. Semin Immunol. 2007; 19 116-126
- 20 Ménager-Marcq I, Pomié C, Romagnoli P, van Meerwijk J P. CD8+ CD28− regulatory T lymphocytes prevent experimental inflammatory bowel disease in mice. Gastroenterology. 2006; 131 1775-1785
- 21 Allez M, Brimnes J, Dotan I, Mayer L. Expansion of CD8+ T cells with regulatory function after interaction with intestinal epithelial cells. Gastroenterology. 2002; 123 1516-1526
- 22 Yu Q T, Saruta M, Avanesyan A, Fleshner P R, Banham A H, Papadakis K A. Expression and functional characterization of FOXP3+ CD4+ regulatory T cells in ulcerative colitis. Inflamm Bowel Dis. 2007; 13 191-199
- 23 Maul J, Loddenkemper C, Mundt P, Berg E, Giese T, Stallmach A, Zeitz M, Duchmann R. Peripheral and intestinal regulatory CD4+ CD25(high) T cells in inflammatory bowel disease. Gastroenterology. 2005; 128 1868-1878
- 24 Brimnes J, Allez M, Dotan I, Shao L, Nakazawa A, Mayer L. Defects in CD8+ regulatory T cells in the lamina propria of patients with inflammatory bowel disease. J Immunol. 2005; 174 5814-5822
- 25 Funakoshi K, Sugimura K, Sasakawa T, Bannai H, Anezaki K, Ishizuka K, Yoshida K, Narisawa R, Asakura H. Study of cytokines in ulcerative colitis. J Gastroenterol. 1995; 30 61-63
- 26 Guimbaud R, Bertrand V, Chauvelot-Moachon L, Quartier G, Vidon N, Giroud J P, Couturier D, Chaussade S. Network of inflammatory cytokines and correlation with disease activity in ulcerative colitis. J Gastroenterol. 1998; 93 2397-2404
- 27 Ma T Y, Iwamoto G K, Hoa N T, Akotia V, Pedram A, Boivin M A, Said H M. TNF-α-induced increase in intestinal epithelial tight junction permeability requires NF-κB activation. Am J Physiol Gastrointest Liver Physiol. 2004; 286 G367-G376
- 28 Sangfelt P, Carlson M, Thörn M, Xu S, Lööf L, Raab Y. Local release of human neutrophil lipocalin (HNL), IL-8, and TNF-α is decreased as response to topical prednisolone treatment in distal ulcerative colitis and proctitis. Dig Dis Sci. 2002; 47 2064-2069
- 29 Rutgeerts P, Sandborn W J, Feagan B G, Reinisch W, Olson A, Johanns J, Travers S, Rachmilewitz D, Hanauer S B, Lichtenstein G R, de Villiers W J S, Present D, Sands B E, Colombel J F. Infliximab for induction and maintenance therapy for ulcerative colitis. N Engl J Med. 2005; 353 2462-2476
- 30 Regueiro M, Curtis J, Plevy S. Infliximab for hospitalized patients with severe ulcerative colitis. J Clin Gastroenterol. 2006; 40 476-481
- 31 Groux H, O'Garra A, Bigler M, Rouleau M, Antonenko S, de Vries J E, Roncarolo M G. A CD4+ T-cell subset inhibits antigen-specific T-cell responses and prevents colitis. Nature. 1997; 389 737-742
- 32 Jijon H B, Churchill T, Malfair D, Wessler A, Jewell L D, Parsons H G, Madsen K L. Inhibition of poly (ADP-ribose) polymerase attenuates inflammation in a model of chronic colitis. Am J Physiol Gastrointest Liver Physiol. 2000; 279 G641-G651
- 33 Van Montfrans C, Rodriguez Pena M S R, Pronk I, Ten Kate F J W, Te Velde A A, Van Deventer S J H. Prevention of colitis by interleukin 10-transduced T lymphocytes in the SCID mice transfer model. Gastroenterology. 2002; 123 1865-1876
Prof. PhD Aiping Lu MD
Institute of Basic Research in Clinical Medicine
China Academy of Chinese Medical Sciences
100700 Beijing
China
Telefon: + 86 10 64 06 76 11
Fax: + 86 10 84 03 28 81
eMail: lap64067611@126.com