Amelioration of experimental colitis by Astragalus membranaceus through anti-oxidation and inhibition of adhesion molecule synthesis

被引:71
作者
Ko, Joshua Ka-Shun [1 ]
Lam, Flora Ying-Lee [1 ]
Cheung, Andrew Pok-Lap [1 ]
机构
[1] Hong Kong Baptist Univ, Sch Chinese Med, Kowloon Tong, Hong Kong, Peoples R China
关键词
IBD; Astragalus membranaceus; Reactive oxygen metabolites; Adhesion molecules;
D O I
10.3748/wjg.v11.i37.5787
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the protective effects of Astragalus membranaceus (Am) against hapten-induced colitis in male Sprague-Dawley rats as well as its underlying mechanism. METHODS: Experimental colitis was induced in rats by enema administration of 2,4-dinitrobenzene sulfonic acid (DNBS). Rats were either pretreated with Am extract (2 or 4 g/kg, p.o. once daily) starting from 10 d before DNBS enema, or received Am post-treatment (2 or 4 g/kg, p.o. twice daily) on the three consecutive days following DNBS administration. Colonic lesion area and histological damage were determined, while the activities of myeloperoxidase (MPO) and xanthine oxidase, as well as reduced glutathione (GSH) content were measured in the excised colonic tissues. Besides, protein expression of inducible nitrite oxide synthase (iNOS), intercellular adhesion molecule-1 (ICAM-1) and P-selectin was also detected by Western blot analysis. RESULTS: Our findings had shown that both macroscopic lesion area and histological colonic damage induced by DNBS were significantly reduced by both Am pre- and post-treatments. These were accompanied by attenuation of the elevated colonic MPO activity and downregulation of the iNOS, P-selectin, and ICAM-1 protein expression. Besides, deprivation of colonic GSH level under colitis condition was also preserved. CONCLUSION: These results demonstrate that Am possesses both preventive and therapeutic potential in experimental colitis. The anti-inflammatory actions involve anti-oxidation along with inhibition of adhesion molecule synthesis in the colonic tissues. (C) 2005 The WJG Press and Elsevier Inc. All rights reserved.
引用
收藏
页码:5787 / 5794
页数:8
相关论文
共 57 条
[31]   Current theories on the causes of inflammatory bowel disease [J].
Papadakis, KA ;
Targan, SR .
GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 1999, 28 (02) :283-+
[32]   CONVERSION OF XANTHINE DEHYDROGENASE TO OXIDASE IN ISCHEMIC RAT INTESTINE - A REEVALUATION [J].
PARKS, DA ;
WILLIAMS, TK ;
BECKMAN, JS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 254 (05) :G768-G774
[33]  
*PHARM COMM PEOPL, 2000, PHARM PEOPL REP CHIN, V1
[34]   ENHANCED COLONIC NITRIC-OXIDE GENERATION AND NITRIC-OXIDE SYNTHASE ACTIVITY IN ULCERATIVE-COLITIS AND CROHNS-DISEASE [J].
RACHMILEWITZ, D ;
STAMLER, JS ;
BACHWICH, D ;
KARMELI, F ;
ACKERMAN, Z ;
PODOLSKY, DK .
GUT, 1995, 36 (05) :718-723
[35]   PEROXYNITRITE-INDUCED RAT COLITIS - A NEW MODEL OF COLONIC INFLAMMATION [J].
RACHMILEWITZ, D ;
STAMLER, JS ;
KARMELI, F ;
MULLINS, ME ;
SINGEL, DJ ;
LOSCALZO, J ;
XAVIER, RJ ;
PODOLSKY, DK .
GASTROENTEROLOGY, 1993, 105 (06) :1681-1688
[36]   Circulating antioxidants in ulcerative colitis and their relationship to disease severity and activity [J].
Ramakrishna, BS ;
Varghese, R ;
Jayakumar, S ;
Mathan, M ;
Balasubramanian, KA .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1997, 12 (07) :490-494
[37]   Xanthine oxidase activity is not increased in the colonic mucosa of ulcerative colitis [J].
Reynolds, PD ;
Rhenius, ST ;
Hunter, JO .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 1996, 10 (05) :737-741
[38]  
RIDDELL RH, 1988, INFLAMM BOWEL DIS, P329
[39]  
Saiki Tomohisa, 1998, Kurume Medical Journal, V45, P69
[40]   Differential role of selectins in experimental colitis [J].
Sans, M ;
Salas, A ;
Soriano, A ;
Prats, N ;
Gironella, M ;
Pizcueta, P ;
Elena, M ;
Anderson, DC ;
Piqué, JM ;
Panés, J .
GASTROENTEROLOGY, 2001, 120 (05) :1162-1172