The role of CCL3/macrophage inflammatory protein-1α in experimental colitis

被引:29
作者
Ajuebor, MN
Kunkel, SL
Hogaboam, CM
机构
[1] Univ Calgary, Fac Med, Gastrointestinal Res Grp, Calgary, AB T2N 4N1, Canada
[2] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
基金
加拿大健康研究院;
关键词
neutrophil; CC chemokine; colitis; inflammation; TNBS;
D O I
10.1016/j.ejphar.2004.07.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
CCL3/macrophage inflammatory protein (MIP-1)-1alpha is elevated in the rectal biopsies of patients with active inflammatory bowel diseases, but its role remains undefined. The present study examined the role of CCL3/MIP-1alpha during trinitrobenzene sulfonic acid (TNBS)induced colitis in the rat. Colonic CCL3/MIP-1alpha levels were elevated (>20-fold above control) within 24 h and remained elevated to day 7 of colitis induction by TNBS administration. In addition, significant increases in colonic neutrophil accumulation were observed within 24 h to day 7 of TNBS treatment. Pre-treatment of rats with a single dose of CCL3/MIP-1alpha antibody significantly reduced (47%) colonic neutrophil accumulation during the early (24 h) phase of TNBS-induced colitis. In contrast, chronic (repeated) administration of CCL3/MIP-1alpha antibody did not attenuate colonic neutrophil accumulation during the late phase (day 7) of TNBS-induced colitis. These results suggest a role for CCL3/MIP-1alpha in promoting colonic neutrophil accumulation during the early (24 h) phase of TNBS-induced colitis. (C) 2004 Elsevier B.V. All fights reserved.
引用
收藏
页码:343 / 349
页数:7
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