Aggravating effect of cigarette smoke exposure on experimental colitis is associated with leukotriene B4 and reactive oxygen metabolites

被引:26
作者
Guo, X
Ko, JKS
Mei, QB
Cho, CH
机构
[1] Univ Hong Kong, Fac Med, Dept Pharmacol, Hong Kong, Hong Kong, Peoples R China
[2] Fourth Mil Med Univ, Dept Pharmacol, Xian 710032, Peoples R China
关键词
cigarette smoke; experimental colitis; leukotriene B-4; reactive oxygen metabolites; glutathione;
D O I
10.1159/000051887
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Cigarette smoking is closely related to the development and recurrence of inflammatory bowel disease (IBD). The present study aimed to investigate the underlying mechanisms of the adverse action of cigarette smoke (CS) exposure on trinitrobenzene sulfonic acid (TNBS)-induced IBD. Methods: Rats were preexposed to CS once daily far 4 days before receiving a TNBS enema, and they were killed 24 h afterwards. The colonic myeloperoxidase (MPO) and xanthine oxidase (XO) activities, leukorriene B-4 (LTB4) and glutathione (GSH) levels, as well as the production of reactive oxygen metabolites (ROMs) were measured. Results: CS preexposure significantly augmented the adverse effects of the TNBS enema on colonic damage and increase in MPO activity, while it did not significantly alter the XO activity. Meanwhile, the elevation of ROM production and LTB4 concentration in colonic tissues after the TNBS enema was also markedly enhanced by CS exposure. in contrast, the depressive action of the TNBS enema on cellular antioxidant GSH levels was reduced further by CS exposure. Pretreatment with a specific LTB4 antagonist, ONO-4057, protected against colonic damage, particularly in the CS group. Conclusions CS exposure aggravated experimental IBD. This adverse action could be due to the depletion of GSH together with overproduction of LTB4, followed by the accumulation of neutrophils and ROMs in the colonic tissue. Copyright (C) 2001 S. Karger AG, Basel.
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页码:180 / 187
页数:8
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