Nakashima Takako, Maeda Takashi, Nagamoto Hisashi, Kumakura Takeshi, Takai Masaaki, Mori Toyoki
Research Institute of Pharmacological and Therapeutical Development, Otsuka Pharmaceutical Co. Ltd., Tokushima 771-0192, Japan.
Dig Dis Sci. 2005 Oct;50 Suppl 1:S124-31. doi: 10.1007/s10620-005-2817-0.
We investigated therapeutic efficacy of rebamipide using dextran sulfate sodium (DSS) induced colitis model in rats. Three percent DSS solution was given to rats for 9 days. After that, we evaluated the drug efficacy on colitis sustained with continuous drinking of 1% DSS. Twice-daily treatment with 0.3% or 1% rebamipide for 14 days significantly ameliorated the stool abnormality in the colitis model, preferentially suppressed hematochezia. The colonic mucosal lesion, determined by Alcian blue staining on day 24, was significantly reduced by rebamipide enema in a dose-dependent manner. Either rebamipide or 5-aminosalycilic acid (5-ASA) enema treated once daily significantly ameliorated colitis. The minimum effective dose of rebamipide was 0.3% in once-daily treatment, and that of 5-ASA was 10%. In a mechanistic study, the epithelial cell sheet formation of the T84 colon cancer cell was measured as an increase in generation of trans-epithelial electrical resistance in vitro. Rebamipide accelerated the increase, while 5-ASA conversely suppressed it. These results suggest that rebamipide enema is effective for treatment of experimental ulcerative colitis (UC).
我们使用葡聚糖硫酸钠(DSS)诱导的大鼠结肠炎模型研究了瑞巴派特的治疗效果。给大鼠饮用3%的DSS溶液,持续9天。之后,我们评估了连续饮用1% DSS维持的结肠炎的药物疗效。每天两次用0.3%或1%的瑞巴派特治疗14天,可显著改善结肠炎模型中的粪便异常,优先抑制便血。在第24天通过阿尔新蓝染色确定的结肠黏膜损伤,瑞巴派特灌肠以剂量依赖的方式显著减轻。瑞巴派特或5-氨基水杨酸(5-ASA)每日灌肠一次均可显著改善结肠炎。瑞巴派特每日一次治疗的最小有效剂量为0.3%,5-ASA为10%。在一项机制研究中,通过测量体外跨上皮电阻的增加来检测T84结肠癌细胞的上皮细胞片形成。瑞巴派特加速了这种增加,而5-ASA则相反地抑制了它。这些结果表明,瑞巴派特灌肠对实验性溃疡性结肠炎(UC)的治疗有效。