Effects of N-Acetylcysteine Plus Mesalamine on Prostaglandin Synthesis and Nitric Oxide Generation in TNBS-Induced Colitis in Rats

被引:35
作者
Ancha, Hanumantha R. [1 ,2 ]
Kurella, Ravi R. [1 ,2 ]
McKimmey, Christine C. [1 ,2 ]
Lightfoot, Stanley [3 ]
Harty, Richard F. [1 ,2 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Med, Div Gastroenterol, Oklahoma City, OK 73104 USA
[2] Vet Affairs Med Ctr, Oklahoma City Dept, Oklahoma City, OK 73104 USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Pathol, Oklahoma City, OK 73104 USA
关键词
N-acetylcysteine plus mesalamine; PGE(2); iNOS in colitis; INFLAMMATORY-BOWEL-DISEASE; SODIUM-INDUCED COLITIS; KAPPA-B; INHIBITION; CYCLOOXYGENASE-2; METABOLITES; CHEMOKINES; PROGRESS; MUCOSA; OXYGEN;
D O I
10.1007/s10620-008-0438-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The aim of the present studies was to examine mechanisms by which the rectally administered combination of N-acetylcysteine (NAC) plus mesalamine (5-ASA) affects inducers of inflammation to promote mucosal healing and reduce tissue inflammation in chemically (trinitrobenzene sulfonic acid, TNBS) induced colitis in rats. Experimental findings demonstrate that dual therapy with NAC plus 5-ASA was superior to individual agents in reducing histological measures of colitis. NAC alone and in combination with 5-ASA suppressed COX2 gene expression and prostaglandin E-2 (PGE(2)) levels to control values. Furthermore, NAC plus 5-ASA reduced nitrate generation, an expression of inducible nitric oxide synthase (iNOS) activity, to basal levels and these results were significantly lower than those observed with either NAC or 5-ASA alone. In conclusion, these results indicate that NAC plus 5-ASA exerts therapeutic benefit, in part by countering the actions of PGE(2) and the deleterious effects of oxidative and nitrosative stress induced by TNBS colitis.
引用
收藏
页码:758 / 766
页数:9
相关论文
共 36 条
[1]   CLINICAL-EVIDENCE SUPPORTING THE RADICAL SCAVENGER MECHANISM OF 5-AMINOSALICYLIC ACID [J].
AHNFELTRONNE, I ;
NIELSEN, OH ;
CHRISTENSEN, A ;
LANGHOLZ, E ;
BINDER, V ;
RIIS, P .
GASTROENTEROLOGY, 1990, 98 (05) :1162-1169
[2]  
Akobeng A K, 2004, Cochrane Database Syst Rev, pCD003574
[3]   Replenishment of glutathione levels improves mucosal function in experimental acute colitis [J].
Ardite, E ;
Sans, M ;
Panés, J ;
Romero, FJ ;
Piqué, JM ;
Fernández-Checa, JC .
LABORATORY INVESTIGATION, 2000, 80 (05) :735-744
[4]  
Bantel H, 2000, AM J GASTROENTEROL, V95, P3452
[5]  
Bonner GF, 2002, AM J GASTROENTEROL, V97, P783
[6]   The metabolic effects of inhibitors of 5-lipoxygenase and of cyclooxygenase 1 and 2 are an advancement in the efficacy and safety of anti-inflammatory therapy [J].
Celotti, F ;
Durand, T .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 2003, 71 (3-4) :147-162
[7]   Anti-inflammatory drugs: New multitarget compounds to face an old problem. The dual inhibition concept [J].
Celotti, F ;
Laufer, S .
PHARMACOLOGICAL RESEARCH, 2001, 43 (05) :429-436
[8]   INHIBITION OF PROSTAGLANDIN BIOSYNTHESIS BY SULFASALAZINE AND ITS METABOLITES [J].
COLLIER, HOJ ;
FRANCIS, AA ;
MCDONALDGIBSON, WJ ;
SAEED, SA .
PROSTAGLANDINS, 1976, 11 (02) :219-225
[9]  
DRYDEN GW, 2007, CURR GASTROENTEROL R, V7, P306
[10]   Non-stop progress in inflammatory bowel disease: new players, new understanding, new therapies [J].
Fiocchi, C .
CURRENT OPINION IN GASTROENTEROLOGY, 2006, 22 (04) :347-348