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C5a适体在三硝基苯磺酸诱导的结肠炎小鼠模型中的有效性。

Effectiveness of C5a aptamers in a TNBS-induced colitis mouse model.

作者信息

Li Zhiping, Wang Xiwen, Chen Man, Wang Yuanyuan, Sun Rui, Qu Han, Sun Yu, Gao Weicun, Li Bo, Dong Xiaolin, Zhang Yandong, Xia Zhiping

机构信息

Key Laboratory of Jilin Province for Zoonosis Prevention and Control, Military Veterinary Institute, Academy of Military Medical Sciences, Changchun, Jilin 130000, P.R. China.

Department of Rheumatology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.

出版信息

Exp Ther Med. 2017 Dec;14(6):6119-6124. doi: 10.3892/etm.2017.5277. Epub 2017 Oct 10.

Abstract

The complement-activated product, complement component 5a (C5a), is a potent inflammatory peptide with a broad spectrum of functions. and studies have demonstrated that C5a serves an important role in inflammation; however, the role of C5a in the pathogenesis of inflammatory bowel disease (IBD) is not known. The purpose of the current study was to investigate the role of C5a in IBD using an experimental mouse model of colitis. Colitis was induced in mice using 2,4,6-trinitrobenzene sulfonic acid (TNBS), and C5a aptamers were subsequently administered via intraperitoneal injection. Clinical symptoms of the disease, histopathological analysis of the colon and the level of inflammatory components were examined. The symptoms of colitis, including changes in behavior, weight loss, colon damage and an increase in inflammatory cytokines, were attenuated following the treatment of mice with TNBS-induced colitis with C5a aptamers. The aptamer-treated mice exhibited a marked attenuation of colitis when compared with untreated mice, as demonstrated by the phenotypic observations, histological examinations and inflammatory cytokine levels. Colitis is characterized by an imbalance between pro-inflammatory and anti-inflammatory mediators. The results of the current study suggest that C5a may serve a critical role in inflammation in IBD.

摘要

补体激活产物补体成分5a(C5a)是一种具有广泛功能的强效炎症肽。并且研究表明C5a在炎症中起重要作用;然而,C5a在炎症性肠病(IBD)发病机制中的作用尚不清楚。本研究的目的是使用实验性小鼠结肠炎模型研究C5a在IBD中的作用。使用2,4,6-三硝基苯磺酸(TNBS)诱导小鼠发生结肠炎,随后通过腹腔注射给予C5a适体。检查了疾病的临床症状、结肠的组织病理学分析以及炎症成分水平。在用C5a适体治疗TNBS诱导的结肠炎小鼠后,结肠炎的症状,包括行为改变、体重减轻、结肠损伤和炎症细胞因子增加,均得到减轻。与未治疗的小鼠相比,适体治疗的小鼠表现出明显的结肠炎减轻,这通过表型观察、组织学检查和炎症细胞因子水平得到证实。结肠炎的特征是促炎介质和抗炎介质之间的失衡。本研究结果表明,C5a可能在IBD的炎症中起关键作用。

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本文引用的文献

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The complement system in inflammatory bowel disease.炎症性肠病中的补体系统。
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Curr Opin Pharmacol. 2010 Oct;10(5):557-62. doi: 10.1016/j.coph.2010.06.009. Epub 2010 Jul 17.

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