Inflammation Drug Discovery Unit, Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Int Immunopharmacol. 2013 Jan;15(1):23-9. doi: 10.1016/j.intimp.2012.10.022. Epub 2012 Nov 6.
The dextran sulfate sodium (DSS)-induced model of colitis is a commonly used model of inflammatory bowel disease (IBD) in animals. However, there were few studies on the therapeutic efficacy of drugs for IBD after the onset of colitis in this model. We established a semi-chronic model of DSS-induced colitis in mice and used it to assess the therapeutic efficacy of agents for IBD.
Colitis was induced by administration of 3% DSS in drinking water to mice for 7days followed by 5days of normal drinking water.
Ulcerative colitis (UC)-like symptoms including diarrhea, bloody stools and body-weight loss were observed from days 3 to 5, and continued until day 12 after DSS administration. Persistent colitis was associated with sustained local production of cytokines and was characterized by infiltration of inflammatory cells, crypt loss and erosion in the distal colon. These features are similar to those found in patients with UC. In this model, anti-tumor necrosis factor (TNF)-α antibody or anti-interleukin (IL)-12/23p40 antibody significantly ameliorated colitis when administered after the onset of colitis. However, treatment with FK506, prednisolone or sulfasalazine provided limited therapeutic benefit.
The DSS-induced colitis established here showed similar symptomatic and histopathological features to those seen in human UC. This model may be available for predicting the clinical efficacy of candidate compounds for UC.
葡聚糖硫酸钠(DSS)诱导的结肠炎模型是动物中常用的炎症性肠病(IBD)模型。然而,在该模型中,结肠炎发病后很少有研究评估 IBD 药物的治疗效果。我们建立了 DSS 诱导的结肠炎半慢性模型,并使用该模型评估 IBD 药物的治疗效果。
通过给小鼠饮用含 3% DSS 的水诱导结肠炎,持续 7 天,然后改为正常饮用水 5 天。
从第 3 天到第 5 天,观察到类似溃疡性结肠炎(UC)的症状,包括腹泻、血便和体重减轻,并持续到 DSS 给药后第 12 天。持续性结肠炎与持续性细胞因子局部产生有关,并表现为远端结肠炎症细胞浸润、隐窝缺失和溃疡。这些特征与 UC 患者的特征相似。在该模型中,抗肿瘤坏死因子(TNF)-α 抗体或抗白细胞介素(IL)-12/23p40 抗体在结肠炎发病后给药可显著改善结肠炎。然而,FK506、泼尼松龙或柳氮磺胺吡啶治疗提供的治疗效果有限。
此处建立的 DSS 诱导的结肠炎在症状和组织病理学特征上与人类 UC 相似。该模型可能可用于预测 UC 候选化合物的临床疗效。